The dipeptidyl peptidase-4 substrate CXCL12 has opposing cardiac effects in young mice
and aged diabetic mice mediated by Ca2+ flux and phosphoinositide 3 kinase γγγγ
Sri N. Batchu1, Karina Thieme
1, Farigol H. Zadeh
2,3, Tamadher A. Alghamdi
1, Veera Ganesh
Yerra1, Mitchell J. Hadden
1, Syamantak Majumder
1, M. Golam Kabir
1, Bridgit B. Bowskill
1,
Danyal Ladha1, Anthony O. Gramolini
2,3, Kim A. Connelly
1, Andrew Advani
1
1Keenan Research Centre for Biomedical Science and Li Ka Shing Knowledge Institute, St.
Michael’s Hospital, Toronto, ON, Canada; 2Department of Physiology, University of Toronto,
Toronto, ON, Canada; 3Ted Rogers Centre for Heart Research, University of Toronto, Toronto,
ON, Canada
Address for correspondence: Dr. Andrew Advani
Associate Professor/Clinician Scientist
St. Michael’s Hospital
6-151 61 Queen Street East
Toronto, Ontario, Canada, M5C 2T2
Tel: 416 864 6060 x8413
Fax: 416 867 3696
Email: [email protected]
Running title: Cardiac actions of DPP-4 substrates; Word count 4,604 words; Total number of
figures 8; Total number of supplementary tables 8; Total number of supplementary figures 1
K.T.’s present address is: Institute of Biomedical Sciences, Department of Physiology and
Biophysics, University of São Paulo, São Paulo, Brazil. S.M.’s present address is: Department
of Biological Sciences, Birla Institute of Technology and Sciences (BITS), Pilani, Rajasthan,
India.
Page 1 of 49 Diabetes
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Diabetes Publish Ahead of Print, published online August 27, 2018
2
ABSTRACT
Blood glucose lowering therapies can positively or negatively affect heart function in Type 2
diabetes, or they can have neutral effects. Dipeptidyl peptidase-4 (DPP-4) inhibitors lower blood
glucose by preventing the proteolytic inactivation of glucagon-like peptide-1 (GLP-1).
However, GLP-1 is not the only peptide substrate of DPP-4. Here, we investigated the GLP-1
independent cardiac effects of DPP-4 substrates. Pointing to GLP-1 receptor (GLP-1R)
independent actions, DPP-4 inhibition prevented systolic dysfunction equally in pressure
overloaded wildtype and GLP-1R knockout mice. Likewise, DPP-4 inhibition or the DPP-4
substrates, substance P or CXCL12 improved contractile recovery following no-flow ischemia in
the hearts of otherwise healthy young adult mice. Either DPP-4 inhibition or CXCL12 increased
phosphorylation of the Ca2+
regulatory protein, phospholamban and CXCL12 directly enhanced
cardiomyocyte Ca2+
flux. In contrast, hearts of aged, obese diabetic mice (which may better
mimic the comorbid patient population) had diminished levels of phospholamban
phosphorylation. In this setting, CXCL12 paradoxically impaired cardiac contractility in a
phosphoinositide 3-kinase γ dependent manner. These findings indicate that the cardiac effects
of DPP-4 inhibition primarily occur through GLP-1R independent processes and that ostensibly
beneficial DPP-4 substrates can paradoxically worsen heart function in the presence of comorbid
diabetes.
Page 2 of 49Diabetes
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Historically overlooked, heart failure is now firmly recognized as being a major long-term
complication of diabetes. On the one hand, diabetes confers an increased risk of heart failure (1).
On the other hand, whereas certain medications used in the treatment of diabetes may reduce the
risk of heart failure (2), others are neutral (3) and some actually increase heart failure risk (4). In
the case of the dipeptidyl peptidase-4 (DPP-4) inhibitor class of anti-hyperglycemic medication
some DPP-4 inhibitors have demonstrated neutrality (e.g. sitagliptin) (3), whereas one
(saxagliptin) was associated with an unexpected increase in risk of hospitalization for heart
failure (5) and another (alogliptin) was associated with a numerical, albeit non-significant,
increase in heart failure risk (6). These observations are generally discordant with most
preclinical studies that have reported overall favorable cardiac effects of various DPP-4
inhibitors (reviewed in (7)).
DPP-4 inhibitors lower blood glucose levels by preventing the enzymatic degradation of the gut
hormones, glucagon-like peptide-1 (GLP-1) and gastric inhibitory polypeptide (GIP) by DPP-4,
a serine exopeptidase. DPP-4 acts by catalyzing the hydrolysis of N-terminal dipeptides from
polypeptides that contain either an alanine or a proline residue at position two. However, GLP-1
and GIP are not the only peptides that possess this amino acid configuration and, as a result,
DPP-4 inhibitors have the capacity to increase the biological activity of a number of other
peptide substrates. Although non-GLP-1 peptide substrates of DPP-4 may not regulate glucose
homeostasis some, such as substance P (8) and C-X-C motif chemokine ligand 12 (CXCL12,
stromal cell-derived factor-1α (SDF-1α)) (9), may play important roles in cardiovascular
(patho)physiology. The increased biological activity of these alternative substrates has been
proposed as mediating some of the cardiovascular effects of DPP-4 inhibitors (10). However, in
Page 3 of 49 Diabetes
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most cases it has not been possible to discern whether the effects of DPP-4 inhibition on
cardiovascular function are mediated by conventional GLP-1 receptor (GLP-1R)-dependent
processes or by alternative DPP-4 substrates.
Here, we hypothesized that the cardiac effects of DPP-4 inhibition are mediated by mechanisms
that do not involve classical GLP-1R mediated events. During the course of our studies we
became mindful of the historical discordance between the effects of DPP-4 inhibition in
experimental rodents and in clinical trials. Accordingly, we went on to compare the effects of
DPP-4 substrates in the hearts of young adult mice, that are typically employed in preclinical
studies, with older obese diabetic mice that may better reflect the comorbid condition of the
patient populations typically studied in cardiovascular outcome trials. Through this comparison,
we discovered a dichotomous effect of the DPP-4 peptide substrate CXCL12, enhancing calcium
(Ca2+
) handling and improving contractility in young hearts but paradoxically impairing cardiac
contractility in aged diabetic hearts in a phosphoinositide 3-kinase γ (PI3Kγ)-dependent manner.
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RESEARCH DESIGN AND METHODS
Dipeptidyl peptidase-4 activity
Plasma DPP-4 activity was determined in wildtype (C57BL/6) mice treated with either normal
chow or linagliptin (0.083g/kg (11)) in chow (Harlan laboratories Inc., Madison, WI), or in the
hearts of diabetic high fat diet-fed (DM-HFD) mice, as previously described (12).
Transverse aortic constriction (TAC) study
GLP-1R-/-
mice were provided by Dr. Daniel J. Drucker at University of Toronto (13). Male
wildtype (C57BL/6) and GLP-1R knockout (GLP-1R-/-
) mice (aged 6-13 weeks) were bred at
Charles River (Sulzfeld, Germany) and they were studied at St. Michael’s Hospital (Toronto,
Ontario, Canada). TAC (or sham) surgery was conducted as previously described (14). Briefly,
a thoracotomy was performed in the second left intercostal space, the aorta was cleared distal to
the subclavian artery and a 7-0 silk suture was used to constrict the aortic arch. Sham surgery
consisted of thoracotomy without placement of an aortic suture. Following TAC surgery, mice
were randomly allocated to receive either linagliptin in chow (0.083g/kg) (11) or chow alone and
they were followed for eight weeks. HbA1c was determined using A1cNow+ (Roxon medi-tech
ltd., Etobicoke, Ontario, Canada). After eight weeks, transthoracic echocardiography was
performed using a high-frequency ultrasound system (Vevo 2100, MS-250 transducer;
VisualSonics Inc., Toronto, Ontario, Canada) and linear dimensions were analyzed offline (Vevo
2100 software v. 1.8) by a single investigator masked to the treatment groups. At sacrifice, mice
were anesthetized, intubated and artificially ventilated. Left ventricular cardiac catheterization
was performed through the right internal carotid artery (Millar Mikro-Tip, 1.4F; AD Instruments,
Page 5 of 49 Diabetes
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Colorado Springs, CO) (15). Data were acquired and analyzed using LabChart Pro (AD
Instruments).
Isolated heart perfusions
Hearts from wildtype (C57BL/6) mice were perfused using a retrograde isolated perfusion
technique as described previously (16). For determination of the effects of DPP-4 peptide
substrates ex vivo, Krebs-Henseleit buffer (KHB) was supplemented with GLP-1 (10nM (17;
18); Bachem, Bubendorf, Switzerland), GLP-2 (10nM (19); Prospec Technologies Inc.,
Mississauga, Ontario, Canada), GIP (10nM (20); Phoenix Pharmaceuticals Inc., Burlingame,
CA), substance P (1µM (21); Tocris Bioscience, Bristol, UK) or CXCL12 (25nM (22);
Shenandoah Biotechnology Inc., Warwick, PA) throughout the procedure. For inhibition of
PI3Kγ, hearts from DM-HFD mice were perfused with IPI-549 (30nM, Chemietek, Indianapolis,
IN) and contractility and heart rate parameters were measured after 20 minutes. The cellular IC50
for IPI-549 is 1.2nM (vs. 250nM for PI3Kα, 240nM for PI3Kß and 180nM for PI3Kδ) (23). Left
ventricular developed pressure (LVDP), maximum and minimum dP/dt and heart rate were
collected and analyzed using PowerLab 8/35 and LabChart Pro (AD Instruments).
High fat diet-fed diabetic mice studies
Male C57BL/6 mice aged eight weeks were obtained from Charles River Laboratories
(Montreal, Quebec, Canada) and placed on a high fat diet (45% kcal fat, 35% kcal carbohydrate,
0.05% wt/wt cholesterol; Research Diets Inc., New Brunswick, NJ). After 12 weeks, mice
received a single intraperitoneal injection of streptozotocin (STZ; 90mg/kg in 0.1M sodium
citrate, pH 4.5). Diabetes was confirmed two weeks after STZ injection by blood glucose testing
Page 6 of 49Diabetes
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(One Touch UltraMini, LifeScan Canada Ltd., Burnaby, BC, Canada) and mice that were not
diabetic (blood glucose <12mmol/L) received a second dose of STZ. Animals were followed for
a total of 26 weeks before hearts were harvested for perfusion in the Langendorff mode.
All experimental procedures adhered to the guidelines of the Canadian Council on Animal Care
and were approved by the St. Michael’s Hospital Animal Care Committee.
Myocyte hypertrophy, nuclear volume and picrosirius red staining
Cardiac myocyte hypertrophy was determined on hematoxylin and eosin (H&E) stained
sections as previously reported (15; 24) and using a method adapted from Frustaci et al (25).
Nuclear volume was determined in 50 cardiomyocytes on each H&E stained sections using a
method adapted from Gerdes et al in which nuclear volume is considered to be that of a
prolate ellipsoid (26). Picrosirius red-stained sections of the left ventricular myocardium were
scanned (Leica Microsystems Inc., Concord, Ontario, Canada) and quantified as the
proportion of positive red staining in 10 randomly chosen fields (x20 magnification) using
ImageScope (Leica Microsystems Inc.).
Quantitative reverse transcriptase PCR (qRT-PCR)
SYBR green based qRT-PCR was performed on a ViiA7 Real-Time PCR System (ThermoFisher
Scientific, Rockford, IL). Primer sequences are listed in Supplemental Table 1. Data analysis
was performed using Applied Biosystems Comparative CT method.
Immunoblotting
Page 7 of 49 Diabetes
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Immunoblotting was performed with antibodies in the following concentrations: phosphorylated
phospholamban (phospho-PLN) (Ser16) 1:1000 (A285 (27)), phospholamban (1D11 (28)),
SERCA2a 1:1000 (IID8F6 (29)), phospho-PLN (Thr17) 1:1000 (sc-17024-R, Santa Cruz
Biotechnology, Dallas, TX), p110γ 1:1000 (sc-166365, Santa Cruz Biotechnology), GAPDH
1:5000 (sc-25778, Santa Cruz Biotechnology). Densitometry was performed using Image J
version 1.39 (National Institutes of Health, Bethesda, MD).
Adult mouse cardiomyocyte isolation and Ca2+ transients measurement
Adult mouse cardiac myocytes were isolated following the protocol developed by Ackerson-
Johnson et al (30). Cells were loaded with 1µM Fura-2AM (ThermoFisher Scientific) and
placed under an Olympus IX81 fluorescence microscope (Tokyo, Japan) with an X-cite 120Q
light source (EXFO, Quebec City, Quebec, Canada; Fura 2B filter set from Semrock, Rochester,
NY). Fura-2AM was excited using single-band excitation (387nm) and emission was recorded
with a single-band filter (510nm). Images were acquired using a Rolera MGi plus EMCCD
camera (QImaging, Surrey, British Columbia, Canada) and analyzed with MetaMorph v7.6.6
software (MetaMorph, Nashville, TN). Cardiac myocytes were stimulated at 5V with a
frequency of 1Hz. After taking control readings, cells were treated with 25nM CXCL12
(Shenandoah Biotechnology Inc.). Ca2+
transients were calculated from 200 frames taken over
one minute.
Phosphodiesterase activity
Phosphodiesterase (PDE) activity was determined in heart homogenates using a PDELight-HTS
cAMP Phosphodiesterase Kit (LT07-600, Lonza Inc., Rockland, ME).
Page 8 of 49Diabetes
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Statistics
Data are expressed as mean ± s.d.. Statistical significance was determined by 1-way ANOVA
with a Fisher least significant difference test for comparison of multiple groups and 2-tailed
Student t test for comparison between two groups. Statistical analyses were performed using
GraphPad Prism 6 for Mac OS X (GraphPad Software Inc., San Diego, CA). A P value less than
0.05 was considered statistically significant.
Page 9 of 49 Diabetes
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RESULTS
DPP-4 inhibition improves left ventricular function in mice with hypertrophic heart failure
through GLP-1R independent mechanisms
In our first experiments, we set out to determine whether the cardiac effects of DPP-4 inhibition
are mediated through GLP-1R dependent or GLP-1R independent actions. Left ventricular
hypertrophy (LVH) is a major determinant of impaired contractile function in Type 2 diabetes
(reviewed in (31)), occurring in up to one third of cases (32). Because mouse models of diabetes
often do not develop LVH (33), we elected to examine the GLP-1R independent effects of DPP-
4 inhibition in mice subjected to transverse aortic constriction (TAC), a model of hypertrophic
heart failure (34). We treated wildtype and GLP-1R-/-
mice with the DPP-4 inhibitor, linagliptin,
which at a dose of 0.083g/kg resulted in a 77.5% reduction in plasma DPP-4 activity (plasma
DPP-4 activity (AU), control (n=5) 640±399, linagliptin (n=6) 144±52, p<0.05). Eight weeks
after TAC surgery, heart weight:tibial length and left ventricular (LV) mass were increased
equivalently in wildtype and GLP-1R-/-
mice (Supplemental Tables 2-5; Figure 1, A and B).
Linagliptin treatment had no effect on LV mass in either wildtype or GLP-1R-/-
mice (Figure 1, A
and B). Heart weight:tibial length was also unaltered with DPP-4 inhibition, although it was
marginally, but non-significantly, lower in linagliptin-treated TAC mice than TAC mice treated
with vehicle (Supplemental Tables 1 and 2). Despite little change in cardiac hypertrophy,
ejection fraction (Figure 1C), fractional shortening (Figure 1D), stroke volume (Figure 1E) and
cardiac output (Figure 1F) were all higher in linagliptin-fed wildtype and linagliptin-fed GLP-
1R-/-
TAC mice in comparison to TAC mice fed normal chow, with an equivalent increase in
each of these measures irrespective of the presence or absence of the GLP-1R (Figure 1C-F).
Page 10 of 49Diabetes
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With respect to hemodynamic parameters, both end systolic pressure and peak systolic pressure
were increased in both wildtype and GLP-1R-/-
TAC mice treated with vehicle or linagliptin and,
like heart weight:tibial length, they were numerically but non-significantly lower with linagliptin
treatment (Supplemental Tables 6 and 7). As we have observed previously (35), the indicator of
diastolic function, Tau was unaltered in TAC mice (Supplemental Tables 6 and 7).
Paralleling the changes in LV mass, cardiomyocyte size, nuclear volume and ß-myosin heavy
chain mRNA levels were increased equivalently in wildtype and GLP-1R-/-
TAC mice, without
significant change with linagliptin treatment (Figure 2, A-D). Likewise, interstitial collagen
deposition was also increased in wildtype and GLP-1R-/-
TAC mice and was unchanged with
DPP-4 inhibition (Figure 2, E and F). In contrast, the preservation of cardiac contractile function
in wildtype and GLP-1R-/-
TAC mice treated with linagliptin was accompanied by an increase in
serine 16 phosphorylation of the Ca2+
handling protein phospholamban (PLN; phospho-PLN
(Ser16)) (Figure 2G), whereas total PLN and SERCA2a levels were unaltered (Figure 2, H and
I).
Linagliptin and the DPP-4 substrates substance P and CXCL12 improve recovery of ex
vivo cardiac contractility following ischemia reperfusion
The equivalent contractility enhancing effects of linagliptin in both TAC wildtype and TAC
GLP-1R-/-
mice suggested to us that at least some of the effects of DPP-4 inhibition are mediated
through GLP-1R independent actions, potentially non-GLP-1 substrates of DPP-4. To
investigate this possibility further we turned to an ex vivo isolated perfused heart system and we
subjected mouse hearts to 20 minutes no-flow ischemia followed by 40 minutes reperfusion. We
Page 11 of 49 Diabetes
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first studied the hearts of wildtype mice fed normal chow or linagliptin in chow. Baseline LVDP
did not differ between the hearts of chow-fed mice and mice treated with linagliptin (Figure 3A).
However, there was an approximate doubling in LVDP with linagliptin after no-flow ischemia
(Figure 3, A and B). Likewise, peak maximum and minimum dP/dt were also increased with
linagliptin after ischemia-reperfusion (Figure 3, C and D). Heart rate did not differ between the
groups either at baseline or following ischemia reperfusion (Figure 3E).
Next, we questioned whether the improvement in post-ischemic recovery with DPP-4 inhibition
could be mimicked by any of the physiological peptide substrates of DPP-4 and we perfused the
hearts of normal chow-fed wildtype mice with one of several different peptides i.e. GLP-1, GLP-
2, GIP, substance P or CXCL12 (36). Forty minutes after 20 minutes no-flow ischemia, LVDP
was significantly increased in substance P perfused hearts and CXCL12 perfused hearts, whereas
GLP-1, GLP-2 and GIP had no effect (Figure 4, A and B). Peak maximum and minimum dP/dt
and heart rate were marginally increased at baseline in GLP-1 perfused hearts, although only
peak minimum dP/dt achieved statistical significance (Figure 4, C and D). Maximum dP/dt,
minimum dP/dt and heart rate did not differ significantly between the various experimental
conditions after no-flow ischemia (Figure 4, C-E).
The DPP-4 substrates substance P and CXCL12 fail to improve post-ischemic recovery in
the hearts of aged, obese diabetic mice and paradoxically worsen basal contractility
Because young mice and aged, diabetic high fat diet-fed mice have recently been reported to
exhibit discordant responses to DPP-4 knockout or inhibition (37), we next set out to determine
whether the contractile effects of either substance P or CXCL12 would be different in the hearts
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of aged, diabetic, high fat diet-fed (DM-HFD) mice (mean body weight 44.4±5.6g , mean blood
glucose 17.5±5.0mmol/L). Plasma DPP-4 activity was increased in DM-HFD mice (plasma
DPP-4 activity (AU) 1102±278 (n=5, p<0.01 vs. control)). Baseline LVDP and peak maximum
and minimum dP/dt did not differ between DM-HFD mice and age-matched non-diabetic normal
chow-fed mice (control) (Figure 5, A-C). However, unlike the hearts of the young adult mice
earlier studied, perfusion of DM-HFD hearts with either substance P or CXCL12 diminished
baseline LVDP and maximum and minimum dP/dt (Figure 5, A-C). Heart rate tended to be
lower in DM-HFD mouse hearts and was significantly lower than age-matched control hearts
after perfusion with either substance P or CXCL12 (Figure 5D). After no-flow ischemia, LVDP
(Figure 5A) and the percentage recovery of LVDP (Figure 5E) were significantly lower in DM-
HFD hearts than age-matched controls. Neither CXCL12 nor substance P improved post-
ischemic recovery in DM-HFD hearts (Figure 5E).
Both the DPP-4 inhibitor linagliptin and the DPP-4 substrate CXCL12 cause
phosphorylation of the regulator of cardiac Ca2+ cycling, PLN
Next, we set out to determine whether DPP-4 inhibition and the DPP-4 substrates, substance P
and CXCL12 activated similar signaling pathways in the hearts of non-diabetic mice subjected to
no-flow ischemia and whether these pathways are altered in DM-HFD hearts. Because we had
observed an increase in PLN (Ser16) phosphorylation in the hearts of TAC mice treated with
linagliptin, we focused our studies on Ca2+
regulatory protein changes. Like in TAC mice,
linagliptin also increased PLN (Ser16) phosphorylation in isolated perfused hearts (Figure 6A).
Interestingly, hearts perfused with CXCL12 also exhibited increased PLN (Ser16)
phosphorylation, whereas hearts perfused with substance P did not (Figure 6A). Total PLN and
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SERCA2a levels were unaffected by any of the conditions (Figure 6, B and C). In contrast,
hearts of DM-HFD mice had markedly diminished levels of phospho-PLN (Ser16), with no
improvement with either CXCL12 or substance P (Figure 6D). We queried whether this
diminution in phospho-PLN (Ser16) could be compensated for by an increase in PLN threonine
17 phosphorylation (phospho-PLN (Thr17)), but similarly found a reduction in phospho-PLN
(Thr17) in DM-HFD hearts (Supplemental Figure 1). As in our earlier experiments in the hearts
of younger, non-diabetic mice, total PLN and SERCA2a levels were unaltered in any of the
experimental groups (Figure 6, E and F). Likewise, transcript levels of the substance P receptor
(NK1 receptor) or the principal receptor for CXCL12 (CXCR4) were unaltered in DM-HFD
hearts (NK1 receptor:RPL13a mRNA (AU) control (age 8-13 weeks, n=4) 1.1±0.4, DM-HFD
(age approximately 8 months, n=4) 1.1±0.2; CXCR4:RPL13a mRNA (AU) control 1.0±0.1, DM-
HFD 1.0±0.1).
PI3Kγγγγ inhibition negates the deleterious effects of CXCL12 on contractile function in aged,
obese diabetic mice
In our final series of experiments, we aimed to discern the mechanism(s) by which a non-GLP-1
DPP-4 substrate may have different effects in the hearts of young adult mice and aged, obese
diabetic mice. For these experiments, we focused on the actions of CXCL12 because, unlike
substance P, CXCL12 mimicked the increase in PLN (Ser16) phosphorylation in the hearts of
young mice caused by linagliptin treatment. In isolated adult mouse ventricular myocytes,
recombinant CXCL12 increased PLN (Ser16) phosphorylation (Figure 7A) and directly
enhanced Ca2+
flux (Figure 7, B-F). In considering how CXCL12 may paradoxically impair
cardiac function in the hearts of DM-HFD mice we recognized the known role of
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phosphodiesterases (PDEs) in limiting PLN phosphorylation (38) and we found PDE activity to
be significantly increased in the hearts of DM-HFD mice (log10 PDE activity (AU), control (n=7,
age 6-13 weeks) 2.3±0.5, DM-HFD (n=12) 2.7±0.3, p<0.05). We observed a general trend
towards an increase in PDE isoform transcript abundance in DM-HFD hearts, mRNA levels of
the PDE4A isoform being significantly increased (2-fold) (Supplemental Table 8). Moreover,
the increase in PDE activity in DM-HFD mouse hearts was accompanied by a marked
upregulation in protein levels of p110γ (Figure 8A), the catalytic subunit of the lipid kinase,
PI3Kγ which is known to regulate PDE activity in cardiomyocytes (39). Because PI3Kγ is
activated by G-protein coupled receptors (GPCRs) (including CXCR4 (40)) and because PI3Kγ
has also been linked to impaired cardiac contractile function (41), we hypothesized that the
deleterious effects of CXCL12 in DM-HFD mice were mediated through the actions of
upregulated PI3Kγ. Consistent with this hypothesis, when we perfused the hearts of DM-HFD
mice with the PI3Kγ inhibitor, IPI-549 concurrently with CXCL12, we found that PI3Kγ
inhibition negated the deleterious effects of CXCL12 on basal LVDP (Figure 8, B-E).
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DISCUSSION
Despite the widespread adoption of DPP-4 inhibitors into the glucose-lowering armamentarium
for the treatment of Type 2 diabetes, several questions remain unanswered regarding their
cardiac effects and the peptide substrates they affect. In the present study, we observed that
DPP-4 inhibition with linagliptin preserved cardiac contractility in pressure-overloaded mouse
hearts even in the absence of the GLP-1R and it also improved contractile recovery of mouse
hearts ex vivo. We went on to discover that this latter effect of linagliptin could be mimicked by
the non-GLP-1 DPP-4 substrate, CXCL12 which enhances cardiomyocyte Ca2+
flux. However,
in the setting of aging, obesity and diabetes, CXCL12 paradoxically worsened cardiac function,
an effect that appeared to be mediated by the lipid kinase, PI3Kγ. Collectively, the findings
highlight the extent to which peptide substrates of DPP-4, other than GLP-1, can affect cardiac
function and they demonstrate how these effects are profoundly influenced by diabetic
comorbidity.
In our first studies, we treated pressure-overloaded wildtype and GLP-1R-/-
mice with the DPP-4
inhibitor linagliptin. We chose a pressure overload model because of the importance of LVH as
a predeterminant of heart failure in diabetes (31). The dosing regimen of linagliptin that we
selected (0.083g/kg) resulted in a 77.5% reduction in plasma DPP-4 activity, just marginally
lower than that observed with the 5mg dose of linagliptin in patients (80-90% (42)). Both
wildtype and GLP-1R-/-
mice exhibited an equivalent reduction in ejection fraction, fractional
shortening, stroke volume and cardiac output following pressure-overload. However, linagliptin-
fed mice demonstrated a notable preservation of systolic function. The preservation of systolic
Page 16 of 49Diabetes
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function with linagliptin is similar to that previously reported with the DPP-4 inhibitor,
vildagliptin (43). However, whereas the cardioprotective effects of vildagliptin were attributed
to improved glucose tolerance and increased GLP-1 levels (43), linagliptin was equally
efficacious in both wildtype and GLP-1R-/-
mice. This led us to conclude that DPP-4 inhibition
has GLP-1 independent cardiac effects and we speculated that these effects are most likely
mediated by the actions of one or more of the other peptide substrates of DPP-4. To help us
discern the similarities between the cardiac effects of DPP-4 inhibition and the cardiac effects of
individual DPP-4 peptide substrates we chose an isolated perfused heart system. Such an
approach allowed us to study the direct cardiac effects of individual peptide substrates of DPP-4
independent of any actions on the central or autonomic system or on preload or afterload.
We examined the effects of five physiological substrates of DPP-4 on LVDP recovery, GLP-1,
GLP-2, GIP, substance P and CXCL12 (44) and we observed that either substance P or CXCL12
improved LVDP recovery, comparable to linagliptin, whereas the other peptides did not. In a
non-reductionist sense, it is not surprising that the effects of linagliptin on the recovery of
contractile function could be mimicked by more than one peptide substrate and, indeed,
substance P (21) and CXCL12 (45) have both been reported to improve contractile recovery
following ischemia reperfusion in other studies. GLP-1 has also been previously reported to
improve the recovery of cardiac contractile function (46), although we did not observe this in the
present study. It is noteworthy, however, that we selected the concentrations of the different
peptide substrates with which to perfuse mouse hearts based on previously reported experiments
(in the absence of data regarding bioequivalence) and thus a direct comparison between the
magnitude of the effect of different peptides should be avoided.
Page 17 of 49 Diabetes
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At this point, our cognizance of the absence of cardiovascular benefit in outcome trials of other
DPP-4 inhibitors reported to date led us to question whether the cardiac effects of either
substance P or CXCL12 would be affected by diabetic comorbidity. To explore this possibility,
we studied the effects of the peptides in the hearts of aged, obese diabetic mice. These mice had
elevated plasma DPP-4 activity and an impairment of LVDP recovery. The increase in plasma
DPP-4 activity is similar to that previously reported in patients with Type 2 diabetes (47). We
observed that substance P or CXCL12 paradoxically impaired basal ex vivo LVDP in diabetic
high fat diet-fed mice and we surmised that this observation was indicative of the persistent
biological activity of the peptides even in the setting of increased plasma DPP-4 activity. We
speculated that the antithetical effects of substance P and CXCL12 in the hearts of young non-
diabetic mice and aged, obese diabetic mice could provide insights into the relative importance
of the signaling pathways the peptides activate and we probed for changes in the proteins that
regulate cardiomyocyte Ca2+
cycling, the signal that regulates cardiac muscle contractility.
The affinity of SERCA2a for Ca2+
is regulated by PLN. In its unphosphorylated state, PLN
limits SERCA2a Ca2+
affinity restricting cardiac contractility, whereas when it is phosphorylated
PLN no longer restricts SERCA2a Ca2+
affinity resulting in positive inotropic and lusitropic
effects (48). PLN can be phosphorylated at two sites, Ser16 (which is mediated by protein
kinase A) and Thr17 (which is mediated by Ca2+
/calmodulin-dependent protein kinase II
(CaMKII)) (49). We found that PLN (Ser16) phosphorylation was increased in the hearts of
wildtype and GLP-1R-/-
TAC mice treated with linagliptin and in the hearts of linagliptin-fed
mice subjected to no-flow ischemia. CXCL12 mimicked this effect of DPP-4 inhibition in
Page 18 of 49Diabetes
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increasing phospho-PLN (Ser16) levels but substance P did not. However, in the hearts of aged,
obese diabetic mice PLN (Ser16) phosphorylation levels were diminished and they were
unaltered by either CXCL12 or substance P. This decrease in PLN (Ser16) phosphorylation
coincided with an increase in PDE activity, which itself is regulated by the lipid kinase, PI3Kγ
(39).
PI3Kγ is a Class IB PI3K that, unlike Class 1A PI3Ks, is activated by GPCRs. PI3Kγ consists of
a catalytic p110γ subunit tightly associated to an accessory or adaptor subunit, p101 (50). Upon
GPCR activation, the Gßγ complex separates from the Gα subunit allowing interaction between
p110γ and the Gßγ complex and resulting in p110γ translocation to the membrane and activation
of its kinase activity. p110γ is expressed by several cardiac cell-types, including cardiomyocytes
(41; 51). PI3Kγ activity is increased in human failing hearts (52) and, in the present study, its
protein levels were increased in the hearts of aged, diabetic high fat diet-fed mice. Loss of p110γ
increases cardiomyocyte contractility (41) through cyclic adenosine monophosphate (cAMP)
dependent mechanisms (53) and its activation in response to ß-adrenergic receptor stimulation
predisposes to myocardial hypertrophy and cardiac fibrosis (51). We hypothesized that the
impairment in LVDP in the CXCL12 perfused hearts of diabetic high fat diet-fed mice was due
to PI3Kγ upregulation and we found that inhibition of PI3Kγ negated the deleterious effects of
CXCL12 on basal LVDP.
A number of limitations of the experiments herein described are worth emphasizing. Firstly, we
studied the effects of linagliptin in vivo in TAC mice and the effects of linagliptin and the
peptides ex vivo in hearts subjected to ischemia reperfusion injury, reflecting our evolving
Page 19 of 49 Diabetes
20
understanding of pathobiological mechanisms during the course of our studies. Accordingly, it
should be appreciated that the pathological processes occurring in the two model systems can be
quite different. However, it is interesting that linagliptin treatment improved the contractility of
the hearts of the young non-diabetic mice in both settings. Likewise, linagliptin (as well as the
GLP-1R agonist, liraglutide) has been reported to improve recovery after myocardial ischemia in
mice in vivo (54). Secondly, although the hearts of linagliptin-treated mice had improved
contractile function that could be mimicked by certain DPP-4 substrates, other than GLP-1, this
does not itself demonstrate that these substrates are responsible for the effects of DPP-4
inhibition in vivo or ex vivo. Commercial antibodies do not typically distinguish between active
and inactive forms of CXCL12 and an increase in active CXCL12 either systemically or locally
within the hearts of linagliptin-treated mice has not been demonstrated. Moreover, even if the
cardiac effects of DPP-4 inhibition in mice are mediated through increased CXCL12 activity, the
actions of endogenously produced active CXCL12 may be different from those of the
recombinant peptide. Thirdly, DPP-4 inhibition does not raise the bioactivity of a single
substrate in isolation and the combined effects of multiple peptides may be quite different from
the effects of any one of them alone. Treatment with the DPP-4 inhibitor MK-0626 impaired
cardiac function in aged, diabetic high fat-diet fed mice subjected to TAC (37). However, a
definitive understanding of the cardiovascular effects specifically of linagliptin in patients with
Type 2 diabetes will be provided by close examination of the results of the CARdiovascular
Outcome Study of LINAgliptin versus glimepiride in patients with Type 2 diabetes
(CAROLINA) and CARdiovascular and renal Microvascular outcomE study with LINAgliptin in
patients with Type 2 diabetes (CARMELINA) clinical trials. Notwithstanding these limitations,
the present experiments do reveal important biological insights that may be helpful in the
Page 20 of 49Diabetes
21
development of new treatment approaches in the future. They also complement, without
contradicting, a recently proposed hypothesis that, in some settings, DPP-4 substrates (including
CXCL12) can have adverse cardiac effects (55).
In summary, DPP-4 inhibition has effects on cardiac function in mice that extend beyond those
mediated by the GLP-1R. Some of these effects can be mimicked by peptide substrates of DPP-
4, other than GLP-1, in particular CXCL12, which has opposing actions in the hearts of young
adult mice and in aged, diabetic high fat diet-fed mice. Whereas CXCL12 enhances
cardiomyocyte Ca2+
handling, it can also impair cardiac contractility in the setting of aging,
obesity and diabetes, the latter effect occurring through PI3Kγ-dependent mechanisms. The
cardiac effects of DPP-4 substrates depend upon the metabolic context in which they act.
Page 21 of 49 Diabetes
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ACKNOWLEDGEMENTS
We thank Youan Liu and Suzanne L. Advani for technical assistance.
FUNDING
S.N.B. was a supported by a Keenan Family Foundation KRESCENT Post-doctoral Fellowship
through the Kidney Foundation of Canada and a Heart and Stroke/Richard Lewar Center of
Excellence Fellowship Award and a Banting and Best Diabetes Centre Hugh Sellers Post-
doctoral Fellowship. K.T. was supported by a Research Internship Abroad from the Sao Paulo
Research Foundation (Fapesp 2016/04591-1). F.H.Z. was supported by a Queen Elizabeth II
Graduate Scholarship in Science and Technology and an Ontario Graduate Scholarship. T.A.A.
is supported by a King Abdullah Foreign Scholarship. M.J.H. is a recipient of a Scholarship
from the Research Training Centre of St. Michael’s Hospital and a Banting and Best Diabetes
Centre - Novo Nordisk Studentship. S.M. was supported by a Diabetes Canada Post-doctoral
Fellowship. A.O.G. was supported by the Heart and Stroke Foundation of Ontario (T-6281).
K.A.C. is a recipient of a Canadian Institutes of Health Research New Investigator Award. A.A.
is a recipient of a Diabetes Investigator Award from Diabetes Canada. These studies were
supported by a grant from Boehringer Ingelheim.
DUALITY OF INTEREST
K.A.C. and A.A. are named as inventors on a patent application by Boehringer Ingelheim for the
use of DPP-4 inhibition in the treatment of heart failure. K.A.C. reports speaker honoraria from
Amgen, AstraZeneca, Boehringer Ingelheim, Eli Lilly, Janssen and Merck; and has received
Page 22 of 49Diabetes
23
research grant support from Amgen, AstraZeneca, Boehringer Ingelheim, Servier, Merck and Eli
Lilly. A.A. has received research support from Boehringer Ingelheim and AstraZeneca.
AUTHOR CONTRIBUTIONS
S.N.B. designed and performed the experiments, analyzed the data and wrote the manuscript.
K.T., F.H.Z., T.A.A., V.G.Y., M.J.H., S.M. and D.L. performed the experiments and analyzed
the data. M.G.K. and B.B. performed the in vivo experiments. A.O.G. supervised the in vitro
experiments. K.A.C. designed the experiments and oversaw the analysis of in vivo assessment of
cardiac function. A.A. designed the experiments, supervised the study and wrote the manuscript.
GUARANTOR STATEMENT
A.A. is the guarantor of this work and, as such, had full access to all the data in the study and
takes responsibility for the integrity of the data and the accuracy of the data analysis.
PRIOR PRESENTATION
Parts of this work were presented at the 76th
and 77th
Scientific Sessions of the American
Diabetes Association, New Orleans, LA (10th
- 14th
June 2016) and San Diego, CA (9th
- 13th
June 2017).
Page 23 of 49 Diabetes
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FIGURE LEGENDS
Figure 1. The DPP-4 inhibitor linagliptin preserves cardiac contractility in pressure-overloaded
wildtype and GLP-1R knockout (GLP-1R-/-
) mice. Echocardiographic parameters in wildtype
and GLP-1R-/-
mice eight weeks after sham surgery or transverse aortic constriction (TAC) and
treated with normal chow or linaglipitin (0.083g/kg) in chow for eight weeks. Wildtype sham +
vehicle, n=15; wildtype sham + linagliptin, n=16; wildtype TAC + vehicle, n=15; wildtype TAC
+ linagliptin, n=13; GLP-1R-/-
sham + vehicle, n=12; GLP-1R-/-
sham + linagliptin, n=12; GLP-
1R-/-
TAC + vehicle, n=17; GLP-1R-/-
TAC + linagliptin, n=11. (A) Representative M-mode
echocardiographs. (B) Left ventricular mass. (C) Ejection fraction. (D) Fractional shortening.
(E) Stroke volume. (F) Cardiac output. Values are mean ± s.d.. *P < 0.05, **P < 0.01, ***P <
0.001 by 1-way ANOVA followed by Fisher least significant difference post hoc test.
Figure 2. Treatment with the DPP-4 inhibitor linagliptin increases phospholamban (PLN)
phosphorylation in the hearts of wildtype and GLP-1R knockout (GLP-1R-/-
) mice. Structural
changes and molecular changes in the hearts of wildtype and GLP-1R-/-
mice eight weeks after
sham surgery or transverse aortic constriction (TAC) and treated with normal chow or
linaglipitin (0.083g/kg) in chow for eight weeks. (A) Representative hematoxylin and eosin-
stained heart sections. Original magnification x400. Scale bar = 50µm. (B and C)
Cardiomyocyte cross sectional area (B) and nuclear volume (C). Wildtype sham + vehicle,
n=14; wildtype sham + linagliptin, n=16; wildtype TAC + vehicle, n=15; wildtype TAC +
linagliptin, n=12; GLP-1R-/-
sham + vehicle, n=11; GLP-1R-/-
sham + linagliptin, n=8; GLP-1R-/-
TAC + vehicle, n=13; GLP-1R-/-
TAC + linagliptin, n=9. (D) ß-myosin heavy chain mRNA
Page 28 of 49Diabetes
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levels. Wildtype sham + vehicle, n=15; wildtype sham + linagliptin, n=14: wildtype TAC +
vehicle, n=14; wildtype TAC + linagliptin, n=12; GLP-1R-/-
sham + vehicle, n=11; GLP-1R-/-
sham + linagliptin, n=12; GLP-1R-/-
TAC + vehicle, n=15; GLP-1R-/-
TAC + linagliptin, n=11.
(E) Representative picosirius red-stained heart sections. Original magnification x400. Scale bar
= 50µm. (F) Proportional picosirius red staining. Wildtype sham + vehicle, n=14; wildtype
sham + linagliptin, n=16; wildtype TAC + vehicle, n=13; wildtype TAC + linagliptin, n=12;
GLP-1R-/-
sham + vehicle, n=9; GLP-1R-/-
sham + linagliptin, n=8; GLP-1R-/-
TAC + vehicle,
n=12; GLP-1R-/-
TAC + linagliptin, n=8. (G) Immunoblotting for PLN phosphorylation on
serine residue 16 (phospho-PLN (Ser16)) (n=4/group). (H) Immunoblotting for total PLN
(n=4/group). (I) Immunoblotting for SERCA2a (n=4/group). AU = arbitrary units. Values are
mean ± s.d.. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001 by 1-way ANOVA followed
by Fisher least significant difference post hoc test.
Figure 3. The DPP-4 inhibitor linagliptin enhances ex vivo contractile recovery after transient
ischemia. Mice were fed linagliptin (0.083g/kg) in chow for one week, hearts were perfused
with Krebs-Henseleit buffer (KHB) and were subjected to 20 minutes no-flow ischemia followed
by 40 minutes reperfusion. Control, n=8; linagliptin, n=9. (A) Left ventricular developed
pressure (LVDP) at baseline and 40 minutes after ischemia reperfusion (R40). (B) Percentage
LVDP recovery. (C) Peak maximum dP/dt. (D) Peak minimum dP/dt. (E) Heart rate. Values
are mean ± s.d.. *P < 0.05, **P < 0.01 by 2-tailed Student t test.
Figure 4. Substance P and CXCL12 enhance ex vivo cardiac function in young adult wildtype
mice. Hearts were perfused with Krebs-Henseleit buffer (KHB) alone (control, n=5) or with
Page 29 of 49 Diabetes
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KHB supplemented with GLP-1 (10nM, n=4), GLP-2 (10nM, n=4), GIP (10nM, n=4), substance
P (1µM, n=4) or CXCL12 (25nM, n=4) throughout the procedure and were subjected to 20
minutes no-flow ischemia followed by 40 minutes reperfusion (R40). (A) Left ventricular
developed pressure (LVDP) at baseline and 40 minutes after ischemia reperfusion (R40). (B)
Percentage LVDP recovery. (C) Peak maximum dP/dt. (D) Peak minimum dP/dt. (E) Heart
rate. Values are mean ± s.d.. *P < 0.05, **P < 0.01, ***P < 0.001 by 1-way ANOVA followed
by Fisher least significant difference post hoc test.
Figure 5. Substance P and CXCL12 impair baseline ex vivo cardiac contractility in aged,
diabetic high fat diet-fed (DM-HFD) mice. Hearts were perfused with Krebs-Henseleit buffer
(KHB) alone or with KHB supplemented with substance P (1µM) or CXCL12 (25nM)
throughout the procedure and were subjected to 20 minutes no-flow ischemia followed by 40
minutes reperfusion (R40). Age-matched control, n=4; DM-HFD, n=5; DM-HFD + substance P,
n=5; DM-HFD + CXCL12, n=4. Of the DM-HFD hearts, one of five perfused with KHB failed
to recover after no-flow ischemia, three of five perfused with substance P failed to recover (so no
error bar shown) and one of four perfused with CXCL12 failed to recover. (A) Left ventricular
developed pressure (LVDP) at baseline and 40 minutes after ischemia reperfusion (R40). (B)
Peak maximum dP/dt. (C) Peak minimum dP/dt. (D) Heart rate. (E) Percentage LVDP
recovery. Values are mean ± s.d.. *P < 0.05, **P < 0.01 by 1-way ANOVA followed by Fisher
least significant difference post hoc test for baseline values and 2-tailed Student t test for R40
values.
Page 30 of 49Diabetes
31
Figure 6. CXCL12 increases phospholamban (PLN) phosphorylation in the hearts of young
adult mice but not in the hearts of aged, diabetic high fat diet-fed mice. Immunoblotting for
Ca2+
-handling proteins in the hearts of young adult mice treated with linagliptin or perfused with
substance P or CXCL12 (A-C) or the hearts of aged, diabetic high fat diet-fed mice (DM-HFD)
perfused with substance P or CXCL12 (D-F) and subjected to no-flow ischemia (n=3/group).
(A) Immunoblotting for phosphorylation of PLN on serine residue 16 (phospho-PLN (Ser16)).
(B) Immunoblotting for total PLN. (C) Immunoblotting for SERCA2a. (D) Immunoblotting for
phospho-PLN (Ser16) in DM-HFD hearts. (E) Immunoblotting for total PLN in DM-HFD
hearts. (F) Immunoblotting for SERCA2a in DM-HFD hearts. AU = arbitrary units. Values are
mean ± s.d.. **P < 0.01 by 1-way ANOVA followed by Fisher least significant difference post
hoc test.
Figure 7. CXCL12 increases Ca2+
flux in cardiomyocytes isolated from young adult mice. (A)
Immunoblotting for phosphorylation of phospholamban (PLN) on serine residue 16 (phospho-
PLN (Ser16)) in cardiomyocytes under control conditions or following exposure to 25nM
CXCL12 for 10 minutes (n=5/condition). (B) Rate of 50% Ca2+
uptake. (C) Overall Ca2+
uptake
rate. (D) Ca2+
release amplitude. (E) Rate of 50% Ca2+
release. (F) Overall Ca2+
release rate.
Control, n=12 individual cells; CXCL12, n=17 individual cells. AU = arbitrary units. Values
are mean ± s.d.. *P < 0.05, **P < 0.01 by 2-tailed Student t test.
Figure 8. Phosphoinositide-3 kinase γ (PI3Kγ) inhibition negates the deleterious effects of
CXCL12 on cardiac contractility in aged, diabetic high fat diet-fed mice (DM-HFD). (A)
Immunoblotting heart homogenates of control or DM-HFD mice for the p110γ subunit of PI3Kγ
Page 31 of 49 Diabetes
32
(n=3/group). (B-E) Effect of PI3Kγ inhibition with IPI-549 (30nM) on the reduction in baseline
left ventricular developed pressure (LVDP) in DM-HFD mouse hearts perfused with CXCL12
(n=4/group). (B) LVDP. (C) Peak maximum dP/dt. (D) Peak minimum dP/dt. (E) Heart rate.
AU = arbitrary units. Values are mean ± s.d.. *P < 0.05, **P < 0.01 by 2-tailed Student t test
(A) and 1-way ANOVA followed by Fisher least significant difference post hoc test (B, C, D, E).
Page 32 of 49Diabetes
Figure 1. The DPP-4 inhibitor linagliptin preserves cardiac contractility in pressure-overloaded wildtype and GLP-1R knockout (GLP-1R-/-) mice. Echocardiographic parameters in wildtype and GLP-1R-/- mice eight
weeks after sham surgery or transverse aortic constriction (TAC) and treated with normal chow or linaglipitin (0.083g/kg) in chow for eight weeks. Wildtype sham + vehicle, n=15; wildtype sham +
linagliptin, n=16; wildtype TAC + vehicle, n=15; wildtype TAC + linagliptin, n=13; GLP-1R-/- sham + vehicle, n=12; GLP-1R-/- sham + linagliptin, n=12; GLP-1R-/- TAC + vehicle, n=17; GLP-1R-/- TAC +
linagliptin, n=11. (A) Representative M-mode echocardiographs. (B) Left ventricular mass. (C) Ejection fraction. (D) Fractional shortening. (E) Stroke volume. (F) Cardiac output. Values are mean +/- s.d.. *P
< 0.05, **P < 0.01, ***P < 0.001 by 1-way ANOVA followed by Fisher least significant difference post hoc test.
215x187mm (300 x 300 DPI)
Page 33 of 49 Diabetes
Figure 2. Treatment with the DPP-4 inhibitor linagliptin increases phospholamban (PLN) phosphorylation in the hearts of wildtype and GLP-1R knockout (GLP-1R-/-) mice. Structural changes and molecular changes in the hearts of wildtype and GLP-1R-/- mice eight weeks after sham surgery or transverse aortic constriction (TAC) and treated with normal chow or linaglipitin (0.083g/kg) in chow for eight weeks. (A) Representative hematoxylin and eosin-stained heart sections. Original magnification x400. Scale bar = 50µm. (B and C) Cardiomyocyte cross sectional area (B) and nuclear volume (C). Wildtype sham + vehicle, n=14; wildtype sham + linagliptin, n=16; wildtype TAC + vehicle, n=15; wildtype TAC + linagliptin, n=12; GLP-1R-/- sham
+ vehicle, n=11; GLP-1R-/- sham + linagliptin, n=8; GLP-1R-/- TAC + vehicle, n=13; GLP-1R-/- TAC +
linagliptin, n=9. (D) ß-myosin heavy chain mRNA levels. Wildtype sham + vehicle, n=15; wildtype sham + linagliptin, n=14: wildtype TAC + vehicle, n=14; wildtype TAC + linagliptin, n=12; GLP-1R-/- sham + vehicle, n=11; GLP-1R-/- sham + linagliptin, n=12; GLP-1R-/- TAC + vehicle, n=15; GLP-1R-/- TAC +
linagliptin, n=11. (E) Representative picosirius red-stained heart sections. Original magnification x400. Scale bar = 50µm. (F) Proportional picosirius red staining. Wildtype sham + vehicle, n=14; wildtype sham + linagliptin, n=16; wildtype TAC + vehicle, n=13; wildtype TAC + linagliptin, n=12; GLP-1R-/- sham
+ vehicle, n=9; GLP-1R-/- sham + linagliptin, n=8; GLP-1R-/- TAC + vehicle, n=12; GLP-1R-/- TAC + linagliptin, n=8. (G) Immunoblotting for PLN phosphorylation on serine residue 16 (phospho-PLN (Ser16))
(n=4/group). (H) Immunoblotting for total PLN (n=4/group). (I) Immunoblotting for SERCA2a (n=4/group). AU = arbitrary units. Values are mean +/- s.d.. *P < 0.05, **P < 0.01, ***P < 0.001,
****P < 0.0001 by 1-way ANOVA followed by Fisher least significant difference post hoc test.
215x166mm (300 x 300 DPI)
Page 34 of 49Diabetes
Figure 3. The DPP-4 inhibitor linagliptin enhances ex vivo contractile recovery after transient ischemia. Mice were fed linagliptin (0.083g/kg) in chow for one week, hearts were perfused with Krebs-
Henseleit buffer (KHB) and were subjected to 20 minutes no-flow ischemia followed by 40 minutes reperfusion. Control, n=8; linagliptin, n=9. (A) Left ventricular developed pressure (LVDP) at baseline and
40 minutes after ischemia reperfusion (R40). (B) Percentage LVDP recovery. (C) Peak maximum dP/dt. (D) Peak minimum dP/dt. (E) Heart rate. Values are mean +/- s.d.. *P < 0.05, **P < 0.01 by 2-
tailed Student t test.
133x121mm (300 x 300 DPI)
Page 35 of 49 Diabetes
Figure 4. Substance P and CXCL12 enhance ex vivo cardiac function in young adult wildtype mice. Hearts were perfused with Krebs-Henseleit buffer (KHB) alone (control, n=5) or with KHB supplemented with GLP-1
(10nM, n=4), GLP-2 (10nM, n=4), GIP (10nM, n=4), substance P (1µM, n=4) or CXCL12 (25nM, n=4) throughout the procedure and were subjected to 20 minutes no-flow ischemia followed by 40 minutes reperfusion (R40). (A) Left ventricular developed pressure (LVDP) at baseline and 40 minutes after
ischemia reperfusion (R40). (B) Percentage LVDP recovery. (C) Peak maximum dP/dt. (D) Peak minimum dP/dt. (E) Heart rate. Values are mean +/- s.d.. *P < 0.05, **P < 0.01, ***P < 0.001 by 1-way ANOVA
followed by Fisher least significant difference post hoc test.
138x90mm (300 x 300 DPI)
Page 36 of 49Diabetes
Figure 5. Substance P and CXCL12 impair baseline ex vivo cardiac contractility in aged, diabetic high fat diet-fed (DM-HFD) mice. Hearts were perfused with Krebs-Henseleit buffer (KHB) alone or with KHB
supplemented with substance P (1µM) or CXCL12 (25nM) throughout the procedure and were subjected to 20 minutes no-flow ischemia followed by 40 minutes reperfusion (R40). Age-matched control, n=4; DM-
HFD, n=5; DM-HFD + substance P, n=5; DM-HFD + CXCL12, n=4. Of the DM-HFD hearts, one of five perfused with KHB failed to recover after no-flow ischemia, three of five perfused with substance P failed to recover (so no error bar shown) and one of four perfused with CXCL12 failed to recover. (A) Left ventricular
developed pressure (LVDP) at baseline and 40 minutes after ischemia reperfusion (R40). (B) Peak
maximum dP/dt. (C) Peak minimum dP/dt. (D) Heart rate. (E) Percentage LVDP recovery. Values are mean +/- s.d.. *P < 0.05, **P < 0.01 by 1-way ANOVA followed by Fisher least significant difference post
hoc test for baseline values and 2-tailed Student t test for R40 values.
194x172mm (300 x 300 DPI)
Page 37 of 49 Diabetes
Figure 6. CXCL12 increases phospholamban (PLN) phosphorylation in the hearts of young adult mice but not in the hearts of aged, diabetic high fat diet-fed mice. Immunoblotting for Ca2+-handling proteins in the hearts of young adult mice treated with linagliptin or perfused with substance P or CXCL12 (A-C) or the hearts of aged, diabetic high fat diet-fed mice (DM-HFD) perfused with substance P or CXCL12 (D-F) and subjected to no-flow ischemia (n=3/group). (A) Immunoblotting for phosphorylation of PLN on serine
residue 16 (phospho-PLN (Ser16)). (B) Immunoblotting for total PLN. (C) Immunoblotting for SERCA2a. (D) Immunoblotting for phospho-PLN (Ser16) in DM-HFD hearts. (E) Immunoblotting for total PLN in DM-HFD hearts. (F) Immunoblotting for SERCA2a in DM-HFD hearts. AU = arbitrary units. Values
are mean +/- s.d.. **P < 0.01 by 1-way ANOVA followed by Fisher least significant difference post hoc test.
180x173mm (300 x 300 DPI)
Page 38 of 49Diabetes
Figure 7. CXCL12 increases Ca2+ flux in cardiomyocytes isolated from young adult mice. (A) Immunoblotting for phosphorylation of phospholamban (PLN) on serine residue 16 (phospho-PLN (Ser16)) in
cardiomyocytes under control conditions or following exposure to 25nM CXCL12 for 10 minutes (n=5/condition). (B) Rate of 50% Ca2+ uptake. (C) Overall Ca2+ uptake rate. (D) Ca2+ release
amplitude. (E) Rate of 50% Ca2+ release. (F) Overall Ca2+ release rate. Control, n=12 individual cells; CXCL12, n=17 individual cells. AU = arbitrary units. Values are mean +/- s.d.. *P < 0.05, **P < 0.01 by
2-tailed Student t test.
143x114mm (300 x 300 DPI)
Page 39 of 49 Diabetes
Figure 8. Phosphoinositide-3 kinase γ (PI3Kγ) inhibition negates the deleterious effects of CXCL12 on cardiac contractility in aged, diabetic high fat diet-fed mice (DM-HFD). (A) Immunoblotting heart
homogenates of control or DM-HFD mice for the p110γ subunit of PI3Kγ (n=3/group). (B-E) Effect of PI3Kγ
inhibition with IPI-549 (30nM) on the reduction in baseline left ventricular developed pressure (LVDP) in DM-HFD mouse hearts perfused with CXCL12 (n=4/group). (B) LVDP. (C) Peak maximum dP/dt. (D) Peak
minimum dP/dt. (E) Heart rate. AU = arbitrary units. Values are mean +/- s.d.. *P < 0.05, **P < 0.01 by 2-tailed Student t test (A) and 1-way ANOVA followed by Fisher least significant difference post hoc test (B,
C, D, E).
147x158mm (300 x 300 DPI)
Page 40 of 49Diabetes
Supplemental Table 1. Primer sequences.
Forward primer sequence (5'→3') Reverse primer sequence (5'→3')
ß-MHC CTACAGGCCTGGGCTTACCT TCTCCTTCTCAGACTTCCGC
NK1 TGGCTCTACAGGCTCGTCA TTCATGTTCGATTTTGCGGTCA
CXCR4 TGCAGCAGGTAGCAGTGAAA TGTATATACTCACACTGATCGGTTC
PDE2A GGTGGCCTCGAAATCTGTGCTGG GCATGCGCTGATAGTCCTTCCG
PDE3A AGAGATTCCGGGGTGGAAGA TGATGCTGGTTCCTGACTGG
PDE4A CTTCTGCGAGACCTGCTCCA GAGTTCCCGGTTCAGCATCC
PDE4B AATGTGGCTGGGTACTCACA AAGGTGTCAGATGAGATTTTAAACG
PDE4D ACCGCCAGTGGACGGACCGGA CATGCCACGCTCCCGCTCTCGG
PDE5A AAATCAATTCAGTTTTGAAGATCC TGTTGAATAGGCCAGGGTTT
RPL13a GCTCTCAAGGTTGTTCGGCTGA AGATCTGCTTCTTCTTCCGATA
ß-MHC = ß-myosin heavy chain; PDE = phosphodiesterase
Page 41 of 49 Diabetes
2
Supplemental Table 2. Metabolic parameters of sham-operated wildtype (WT) mice or WT
mice undergoing transverse aortic constriction (TAC) surgery and treated with vehicle or
linagliptin for eight weeks.
WT sham +
vehicle
WT sham +
linagliptin
WT TAC +
vehicle
WT TAC +
linagliptin
n 15 16 15 13
Body weight (g) 29±3 30±2 29±3 31±3
Heart weight (mg) 164±25 153±21 205±62ab 182±37
Heart weight:body weight
(mg/g)
5.6±0.8 5.1±0.9 7.3±2.8bc 5.8±1.1d
Heart weight:tibial length
(mg/mm)
8.8±1.6 7.6±1.7 10.9±3.6ce 9.9±2.6f
Lung weight (mg) 186±32 195±36 215±67 219±57
HbA1c (%) 4.6±0.3 4.7±0.2 4.8±0.3 4.6±0.2
HbA1c (mmol/mol) 26.9±3.3 28.1±2.4 28.7±3.0 26.4±2.4
Values are mean ± s.d.. aP < 0.01 vs. WT sham + vehicle, bP < 0.001 vs. WT sham + linagliptin,
cP < 0.05 vs. WT sham + vehicle, dP < 0.05 vs. WT TAC + vehicle, eP < 0.01 vs. WT sham +
linagliptin, fP < 0.05 vs. WT sham + linagliptin, by 1-way ANOVA followed by Fisher least
significant difference post hoc test.
Page 42 of 49Diabetes
3
Supplemental Table 3. Metabolic parameters of sham-operated GLP-1R knockout (GLP-
1R-/-) or GLP-1R-/- mice undergoing transverse aortic constriction (TAC) surgery and treated
with vehicle or linagliptin for eight weeks.
GLP-1R-/- sham
+ vehicle
GLP-1R-/- sham
+ linagliptin
GLP-1R-/- TAC
+ vehicle
GLP-1R-/- TAC
+ linagliptin
n 12 12 17 11
Body weight (g) 28±2 28±2 28±3 27±3
Heart weight (mg) 159±20 161±30 204±53ab 195±38cd
Heart weight:body
weight (mg/g)
5.7±0.7 5.9±0.9 7.4±2.0ad 7.4±1.9cd
Heart weight:tibial length
(mg/mm)
8.4±1.2 8.3±0.2 11.0±2.7ab 10.5±2.2cd
Lung weight (mg) 204±46 165±35 181±32 225±77be
HbA1c (%) 4.8±0.3 4.6±0.4 4.8±0.4 4.7±0.3
HbA1c (mmol/mol) 29.2±3.7 27.1±4.1 28.7±3.8 28.4±1.7
Values are mean ± s.d.. aP < 0.01 vs. GLP-1R-/- sham + vehicle, bP < 0.01 vs. GLP-1R-/- sham +
linagliptin, cP < 0.05 vs. GLP-1R-/- sham + vehicle, dP < 0.05 vs. GLP-1R-/- sham + linagliptin,
eP < 0.05 vs. GLP-1R-/- TAC + vehicle, by 1-way ANOVA followed by Fisher least significant
difference post hoc test.
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4
Supplemental Table 4. Heart rate and chamber dimensions determined by M-mode
echocardiography in sham-operated wildtype (WT) mice or WT mice undergoing transverse
aortic constriction (TAC) surgery and treated with vehicle or linagliptin for eight weeks.
WT sham +
vehicle
WT sham +
linagliptin
WT TAC +
vehicle
WT TAC +
linagliptin
Heart rate (bpm) 385±52 393±58 355±64 425±67a
LVDs (mm) 3.0±0.4 2.7±0.6 3.4±1.1b 2.7±0.6c
LVDd (mm) 4.2±0.4 4.0±0.4 4.3±0.9 4.0±0.4
LVESV (µl) 37±12 29±14 42±19d 29±16e
LVEDV (µl) 80±18 71±16 90±55 72±15
LVAWT (mm) 4.2±0.4 3.9±0.4 4.3±0.9 3.9±0.4
LVPWT (mm) 0.8±0.2 0.8±0.2 1.0±0.2df 0.9±0.2g
bpm = beats per minute, LVDs = left ventricular internal diameter at systole, LVDd = left
ventricular internal diameter at diastole, LVESV = left ventricular end systolic volume, LVEDV
= left ventricular end diastolic volume, LVAWT = left ventricular anterior wall thickness, LVPWT
= left ventricular posterior wall thickness
Values are mean ± s.d.. aP < 0.01 vs. WT TAC + vehicle, bP < 0.01 vs. WT sham + linagliptin, cP
< 0.01 vs. WT TAC + vehicle, dP < 0.05 vs. WT sham + linagliptin, eP < 0.05 vs. WT TAC +
vehicle, fP < 0.01 vs. WT sham + vehicle, gP < 0.05 vs. WT sham + vehicle, by 1-way ANOVA
followed by Fisher least significant difference post hoc test.
Page 44 of 49Diabetes
5
Supplemental Table 5. Heart rate and chamber dimensions determined by M-mode
echocardiography in sham-operated GLP-1R knockout (GLP-1R-/-) mice or GLP-1R-/- mice
undergoing transverse aortic constriction (TAC) surgery and treated with vehicle or
linagliptin for eight weeks.
GLP-1R-/- sham
+ vehicle
GLP-1R-/- sham
+ linagliptin
GLP-1R-/- TAC
+ vehicle
GLP-1R-/- TAC
+ linagliptin
Heart rate (bpm) 424±73 390±57 377±78 404±72
LVDs (mm) 2.8±0.6 3.2±0.7 3.6±0.7a 3.0±0.6b
LVDd (mm) 4.0±0.4 4.3±0.4 4.4±0.6 4.2±0.3
LVESV (µl) 31±17 44±19 57±29 47±32
LVEDV (µl) 73±17 85±19 91±28 90±33
LVAWT (mm) 4.0±0.4 4.2±0.5 4.4±0.6 4.2±0.7
LVPWT (mm) 0.8±0.2 0.8±0.1 0.9±0.1 1.0±0.2cd
bpm = beats per minute, LVDs = left ventricular internal diameter at systole, LVDd = left
ventricular internal diameter at diastole, LVESV = left ventricular end systolic volume, LVEDV
= left ventricular end diastolic volume, LVAWT = left ventricular anterior wall thickness, LVPWT
left ventricular posterior wall thickness
Values are mean ± s.d.. aP < 0.01 vs. GLP-1R-/- sham + vehicle, bP < 0.05 vs. GLP-1R-/- TAC +
vehicle, cP < 0.05 vs. GLP-1R-/- sham + vehicle, dP < 0.05 vs. GLP-1R-/- sham + linagliptin, by 1-
way ANOVA followed by Fisher least significant difference post hoc test.
Page 45 of 49 Diabetes
6
Supplemental Table 6. Invasive hemodynamic parameters in sham-operated wildtype (WT)
mice or WT mice undergoing transverse aortic constriction (TAC) surgery and treated with
vehicle or linagliptin for eight weeks.
WT sham +
vehicle
WT sham +
linagliptin
WT TAC +
vehicle
WT TAC +
linagliptin
Ejection fraction (%) 57±14 61±8 41±28a 61±23b
Pmax (mmHg) 93±11 102±11 153±26cd 152±30cd
ESP (mmHg) 89±13 97±12 144±24c 135±32c
EDP (mmHg) 13±7 13±8 14±5 17±10
dP/dt max (mmHg/sec) 5281±1744 6965±2230 8022±2350e 7570±2436a
dP/dt min (mmHg/sec) -4712±1712 -6249±1605 -7496±2141f -6622±1365a
Tau (ms) 12.5±3.3 10.8±3.8 9.5±2.3 10.1±2.3
Pmax = maximum pressure (peak systolic pressure), ESP = end systolic pressure, EDP = end
diastolic pressure
Values are mean ± s.d.. aP < 0.05 vs. WT sham + vehicle, bP < 0.05 vs. WT TAC + vehicle, cP <
0.0001 vs. WT sham + vehicle, dP < 0.0001 vs. WT sham + linagliptin, eP < 0.01 vs. WT sham +
vehicle, fP < 0.001 vs. WT sham + vehicle, by 1-way ANOVA followed by Fisher least significant
difference post hoc test.
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Supplemental Table 7. Invasive hemodynamic parameters in sham-operated GLP-1R
knockout (GLP-1R-/-) mice or GLP-1R-/- mice undergoing transverse aortic constriction
(TAC) surgery and treated with vehicle or linagliptin for eight weeks.
GLP-1R-/- sham
+ vehicle
GLP-1R-/- sham
+ linagliptin
GLP-1R-/- TAC
+ vehicle
GLP-1R-/- TAC
+ linagliptin
Ejection fraction (%) 59±11 48±12 44±13a 50±16
Pmax (mmHg) 100±11 104±10 143±31bc 128±19de
ESP (mmHg) 96±11 102±10 137±31bf 119±20a
EDP (mmHg) 10±4 16±8 16±7 14±9
dP/dt max (mmHg/sec) 6716±1893 6334±831 6461±2340 5735±1648
dP/dt min (mmHg/sec) -5874±1200 -5633±968 -6157±1957 -5932±1701
Tau (ms) 10.2±2.2 11.6±3.0 11.4±3.2 10.9±2.0
Pmax = maximum pressure (peak systolic pressure), ESP = end systolic pressure, EDP = end
diastolic pressure
Values are mean ± s.d.. aP < 0.05 vs. GLP-1R-/- sham + vehicle, bP < 0.0001 vs. GLP-1R-/- sham
+ vehicle, cP < 0.0001 vs. GLP-1R-/- sham + linagliptin, dP < 0.01 vs. GLP-1R-/- sham + vehicle,
eP < 0.05 vs. GLP-1R-/- sham + linagliptin, fP < 0.001 vs. GLP-1R-/- sham + linagliptin, by 1-way
ANOVA followed by Fisher least significant difference post hoc test.
Page 47 of 49 Diabetes
8
Supplemental Table 8. Phosphodiesterase (PDE) isoform mRNA levels in the hearts of non-
obese, non-diabetic mice aged 6-13 weeks (young) or aged approximately 8 months (age-
matched) or diabetic high fat-diet (DM-HFD) mice aged approximately 8 months.
Young hearts Age-matched hearts DM-HFD hearts
PDE2A 1.00±0.04 1.08±0.14 1.46±1.11
PDE3A 1.00±0.05 1.06±0.10 1.65±1.10
PDE4A 1.09±0.50 1.00±0.38 2.05±0.64ab
PDE4B 1.01±0.16 0.98±0.36 1.19±1.03
PDE4D 1.00±0.10 0.95±0.19 1.71±1.13
PDE5A 1.00±0.05 0.88±0.06 1.21±0.85
Values are normalized to RPL13a and are expressed as mean ± s.d.. n=4/group. aP < 0.05 vs.
young hearts, bP < 0.05 vs. age-matched hearts by 1-way ANOVA followed by Fisher least
significant difference post hoc test.
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9
Supplemental Figure 1. Phospholamban (PLN) phosphorylation on threonine residue 17 (phospho-PLN (Thr17)) is reduced in the hearts of diabetic high fat diet-fed (DM-HFD) mice and unaffected by substance P or CXCL12. Immunoblotting for phospho-PLN (Thr17) in DM-HFD hearts (n=3/group). AU = arbitrary units. Values are mean ± s.d.. *P < 0.05 by 1-way ANOVA followed by Fisher least significant difference post hoc test.
Page 49 of 49 Diabetes