Dipeptidyl Peptidase 4 Is a Novel Adipokine Potentially Linking Obesity to the Metabolic Syndrome
- Daniela Lamers1,
- Susanne Famulla1,
- Nina Wronkowitz1,
- Sonja Hartwig2,
- Stefan Lehr2,
- D. Margriet Ouwens2,
- Kristin Eckardt1,
- Jean M. Kaufman3,
- Mikael Ryden4,
- Stefan Müller5,
- Franz-Georg Hanisch5,
- Johannes Ruige3,
- Peter Arner4,
- Henrike Sell1 and
- Juergen Eckel1⇓
- 1Paul-Langerhans-Group, German Diabetes Center, Duesseldorf, Germany
- 2Institute of Clinical Biochemistry and Pathobiochemistry, German Diabetes Center, Duesseldorf, Germany
- 3Department of Endocrinology, Ghent University Hospital, Ghent, Belgium
- 4Department of Medicine, Karolinska Institute at Karolinska Hospital, Stockholm, Sweden
- 5Institute of Biochemistry II, Medical Faculty, University of Cologne, Cologne, Germany
- Corresponding author: Juergen Eckel, .
D.L., S.F., and N.W. contributed equally to the work.
OBJECTIVE Comprehensive proteomic profiling of the human adipocyte secretome identified dipeptidyl peptidase 4 (DPP4) as a novel adipokine. This study assessed the functional implications of the adipokine DPP4 and its association to the metabolic syndrome.
RESEARCH DESIGN AND METHODS Human adipocytes and skeletal and smooth muscle cells were used to monitor DPP4 release and assess the effects of soluble DPP4 on insulin signaling. In lean and obese subjects, depot-specific expression of DPP4 and its release from adipose tissue explants were determined and correlated to parameters of the metabolic syndrome.
RESULTS Fully differentiated adipocytes exhibit a substantially higher release of DPP4 compared with preadipocytes or macrophages. Direct addition of DPP4 to fat and skeletal and smooth muscle cells impairs insulin signaling. A fivefold higher level of DPP4 protein expression was seen in visceral compared with subcutaneous fat of obese patients, with no regional difference in lean subjects. DPP4 serum concentrations significantly correlated with adipocyte size. By using adipose tissue explants from lean and obese subjects, we observed a twofold increase in DPP4 release that strongly correlated with adipocyte volume and parameters of the metabolic syndrome and was decreased to the lean level after weight reduction. DPP4 released from adipose tissue correlated positively with an increasing risk score for the metabolic syndrome.
CONCLUSIONS DPP4 is a novel adipokine that may impair insulin sensitivity in an autocrine and paracrine fashion. Furthermore, DPP4 release strongly correlates with adipocyte size, potentially representing an important source of DPP4 in obesity. Therefore, we suggest that DPP4 may be involved in linking adipose tissue and the metabolic syndrome.
Obesity is the hallmark of the metabolic syndrome and represents a major global health problem that frequently associates with the development of chronic diseases, including type 2 diabetes and cardiovascular disease (1). A complex interorgan cross-talk scenario between adipose tissue and other central and peripheral organs underlies the progression of these diseases, with adipose tissue on top of the cross-talk hierarchy (2). This is attributed to the huge diversity of signaling and mediator molecules released from adipose tissue, which is now considered one of the major endocrine organs (3,4). Recent data show that adipokines, which are proteins and peptides released by various adipose tissue cells, create a complex interconnected network of feedback loops (5). Enlargement of adipose tissue leads to dysregulation of adipokine secretion, representing a potential critical pathogenic link among obesity, insulin resistance (IR), and type 2 diabetes (1). Therefore, we conducted a comprehensive proteomic profiling of conditioned media derived from differentiated, primary human adipocytes. This resulted in the identification of novel adipokines, including the exoprotease dipeptidyl peptidase 4 (DPP4).
DPP4 is a ubiquitously expressed transmembrane glycoprotein that cleaves N-terminal dipeptides from a variety of substrates, including growth factors and hormones, neuropeptides, and chemokines (6). Two substrates of DPP4, glucagon-like peptide-1 (GLP-1) and gastric inhibitory polypeptide (GIP), are released from the intestinal mucosa and responsible for ∼60% of postprandial insulin secretion, the so-called incretin effect (7). Because GLP-1 remains active under hyperglycemic conditions in type 2 diabetes, DPP4 has gained considerable interest as a therapeutic target, and a variety of DPP4-inhibitors that prolong the insulinotropic effect of GLP1 are now in clinical use as antidiabetic drugs (8). Substantial DPP4 activity is also found in plasma and other body fluids because of a soluble form of DPP4 lacking the cytoplasmic tail and the transmembrane region of this protein (9). Both the membrane abundance and the circulating activity of DPP4 have been found to be altered in a variety of neurologic and inflammatory diseases (6). However, although a fraction of soluble DPP4 most likely originates from cells of the immune system (10), the major source of circulating DPP4 and its regulation remain unknown.
Furthermore, essentially no data are currently available regarding the potential effects of soluble DPP4 on insulin target tissues, including muscle and fat. In the present investigation, we combined in vitro experiments with two independent clinical studies, aiming to validate DPP4 as a novel adipokine and to characterize the association of DPP4 to different parameters of the metabolic syndrome. We show that 1) DPP4 is a novel adipokine released from differentiated human adipocytes and that it may exert autocrine and paracrine effects leading to IR; 2) DPP4 expression is substantially elevated in visceral fat of obese subjects and that serum DPP4 correlates with adipocyte size and all parameters of the metabolic syndrome; and 3) adipose tissue explants from obese subjects release substantially more DPP4 with a prominent decrease after weight reduction. In light of the well accepted interference of DPP4 with the incretin system, we now suggest that DPP4 may play a role in linking obesity to IR and the metabolic syndrome.
RESEARCH DESIGN AND METHODS
Reagents for SDS-PAGE were supplied by GE Healthcare (Freiburg, Germany) and Sigma-Aldrich (Munich, Germany). Polyclonal antibodies for adiponectin and actin were supplied by Abcam (Cambridge, U.K.). Horseradish peroxidase (HRP)-conjugated goat anti-rabbit and goat anti-mouse IgG antibodies were supplied by Promega (Mannheim, Germany). Collagenase NB4 was obtained from Serva (Heidelberg, Germany). Troglitazone, tumor necrosis factor (TNF)-α, and BSA (fraction V, fatty acid free, low endotoxin) were obtained from Sigma-Aldrich. Adiponectin was purchased from Biovendor (Heidelberg, Germany). Complete protease inhibitor cocktail and PhosStop phosphatase inhibitor cocktail were provided by Roche (Mannheim, Germany). FCS was supplied by Gibco (Invitrogen, Carlsbad, CA). All other chemicals were of the highest analytic grade commercially available and purchased from Sigma-Aldrich. Human recombinant DPP4 was purchased from R&D Systems (Wiesbaden-Nordenstadt, Germany), and a polyclonal antibody was purchased from Abnova (Heidelberg, Germany). The specific DPP4 inhibitor K579 was purchased from Biozol (Eching, Germany).
Clinical studies of DPP-4 concentration in serum and DPP4 release from adipose tissue
For all studies, protocols were approved by local ethics committees, and all participants gave written, informed consent.
Study 1 included 20 male obese patients and 20 lean controls who were recruited at Gent University Hospital (Belgian registration number B67020084018). For all patients, anthropometric and routine blood parameters were assessed. Fasting blood samples were collected, and adipose tissue biopsies were fixed for microscopic evaluation of adipocyte surface area analysis.
Study 2 included 19 obese (BMI ≥30 kg/m2) otherwise healthy and 10 lean (BMI <25 kg/m2) healthy women who were recruited at Karolinska Institute and investigated in the morning after an overnight fast. Sixteen obese women were reinvestigated 18–24 months after gastric bypass in a weight-stable period for at least 3 months, according to self-report (reduction of BMI from 43.0 to 27.9 kg/m2). A venous blood sample was obtained for the analysis of glucose and insulin to be used as an estimation of insulin sensitivity in vivo with the homeostasis model assessment (HOMA) index as described (11). Thereafter, abdominal subcutaneous adipose tissue biopsies were obtained by needle aspiration as described previously (12). One part of the tissue was used for measurements of DPP4 release as described previously (13). Methodological experiments revealed that DPP4 release was linear with time for at least 3 h, suggesting no important cell damage (data not shown). Another part of the tissue was subjected to collagenase treatment, and mean adipocyte volume and weight were determined as described previously (14).
For calculation of the risk score for the metabolic syndrome, we used Adult Treatment Panel-III definitions as follows: 1) fasting glucose >110 mg/dL or diagnosis of type 2 diabetes, 2) blood pressure >135/85 mmHg, 3) serum triglycerides >150 mg/dL, 4) HDL-cholesterol <40 mg/dL for men and <50 mg/dL for women, and 5) abdominal obesity characterized by a waist >102 cm for men and >88 cm for women. The risk score is equal to the number of criteria fulfilled. Subjects with a risk score of ≥3 are qualified as having the metabolic syndrome.
HOMA for IR was determined in all patients, with the exception of those treated with insulin, by a mathematic transformation of fasting blood glucose and insulin measurements (HOMA = insulin [μU/mL] × glucose [mmol/L]/22.5).
Adipocyte isolation and culture
Subcutaneous adipose tissue was obtained from lean or moderately overweight women undergoing plastic surgery for mammary reduction or breast reconstruction with subcutaneous abdominal adipose tissue. The procedure was approved by the ethical committee of the Heinrich-Heine-University (Düsseldorf, Germany). All subjects were healthy and free of medication and had no evidence of diabetes according to routine laboratory test results. Preadipocytes were isolated by collagenase digestion of adipose tissue as previously described by Dietze-Schroeder et al. (15). Isolated cell pellets were resuspended in Dulbecco’s modified Eagle’s medium/Ham’s F12 (DMEM/F12) medium supplemented with 10% FCS. After overnight incubation, cultures were washed and further incubated in an adipocyte differentiation medium (DMEM/F12, 33 μmol/L biotin, 17 μmol/L d-pantothenic acid, 66 nmol/L insulin, 1 nmol/L triiodo-l-thyronine, 100 nmol/L cortisol, 10 μg/mL apotransferrin, 50 μg/μL gentamycin, 15 mmol/L HEPES, and 14 nmol/L NaHCO3, pH 7.4) for 15 days with medium change every 2–3 days and the addition of 5 μmol/L troglitazone for the first 3 days. The degree of differentiation was determined by Oil Red staining and induction of adiponectin expression. Differentiated adipocytes were used for the generation of adipocyte-conditioned media, as recently described by Dietze-Schroeder et al. (15). In brief, after in vitro differentiation, adipocytes were washed and incubated for 48 h in α-modified DMEM followed by collection of the medium. Macrophages were isolated from human adipose tissue and cultured using a method described by Curat et al. (16). For hypoxia treatment, differentiated adipocytes were incubated with a gas mixture containing 1% O2, 5% CO2, and 94% N2 in MIC-101 modular incubator chambers (Billups-Rothenburg, Del Mar, CA) at 37°C for the indicated times.
Skeletal muscle cell culture
Primary human skeletal muscle cells of healthy Caucasian donors were supplied as proliferating myoblasts (5 × 105 cells) and cultured as described previously (15). For an individual experiment, myoblasts were seeded in six-well culture dishes (9.6 cm2/well) at a density of 105 cells per well and cultured in α-modified DMEM/F12 medium containing skeletal muscle cell growth medium supplement pack up to near confluence. The cells were then differentiated and fused by culture in α-modified DMEM for 4 days and used for experiments.
Smooth muscle cell culture and proliferation
Primary human coronary artery smooth muscle cells were obtained from PromoCell (Heidelberg, Germany). Cells from four different donors were supplied as proliferating cells and kept in culture according to the manufacturer’s protocol. For all experiments, subconfluent cells of passage three were used. Cells were characterized as smooth muscle cells by morphologic criteria and by immunostaining with smooth muscle α-actin.
Adipocytes and macrophages were treated as indicated and lysed in a buffer containing 50 mmol/L HEPES, pH 7.4, 1% Triton X-100, complete protease inhibitor, and PhosStop phosphatase inhibitor cocktail. After incubation for 2 h at 4°C, the suspension was centrifuged at 10,000g for 15 min. Thereafter, 5–10 μg adipocyte lysates were separated by SDS-PAGE using 10% horizontal gels and transferred to polyvinylidene fluoride filters in a semidry blotting apparatus. Filters were blocked with Tris-buffered saline containing 0.1% Tween and 5% nonfat dry milk and subsequently incubated overnight with a 1:1,000 dilution of the appropriate antibodies. After washing, filters were incubated with secondary HRP-coupled antibody and processed for enhanced chemiluminescence detection using Immobilon HRP substrate (Millipore, Billerica, MA). Signals were visualized and evaluated on a LUMI Imager (Boehringer, Mannheim, Germany) or VersaDoc 4000 MP (Bio-Rad Laboratories, Munich, Germany) work station.
DPP4 and heme oxygenase-1 secretion by human primary adipocytes and macrophages were determined using ELISA kits purchased from R&D Systems and Streegen Biotechnologies (Lörrach, Germany). The assays were performed in duplicates according to the manufacturer’s instructions.
Presentation of data and statistics
Data are expressed as mean ± SEM. The Shapiro–Wilcoxon test was used to test the Gaussian distribution of biological parameters. Student t test and ANOVA followed by P for linear trend post-test when appropriate were used for comparison between groups. Correlations were performed by Pearson. For adjustment (BMI, age), we applied a multiple linear regression modeling using least-squares means tests. All statistical analyses were done using JMP statistics software (SAS Institute Inc., Cary, NC) or Prism (GraphPad Software, Inc., La Jolla, CA) considering a P value <0.05 as statistically significant. Corresponding significance levels are indicated in Figs. 1 to 7.
DPP4 is a novel adipokine exhibiting regulated release from human adipocytes
Comprehensive proteomic profiling of the adipocyte secretome led to the identification of 347 proteins, with 263 proteins being predicted or annotated as secretory proteins (data to be presented in another publication). Although ∼80% of these proteins have been reported in earlier studies (17–19), our approach has identified >40 novel adipokines, including DPP4.
To validate this novel adipokine, we used in vitro differentiated human adipocytes and macrophages isolated from adipose tissue. DPP4 expression in human adipocytes is significantly increased during differentiation with a maximum reached at day 7 (fourfold over undifferentiated control) (Fig. 1A). DPP4 expression is paralleled by a marked release of this adipokine (Fig. 1B), which was significantly elevated compared with the undifferentiated control starting at day 4 and increasing up to day 9 (1.1 ng/mL released over 24 h by 3.5 × 105 cells). DPP4 in the supernatant of adipocytes was quantified by ELISA and confirmed by Western blotting (Fig. 1B). We further analyzed the release of DPP4 with prominent regulators of adipocyte secretory activity, such as troglitazone, TNF-α, insulin, and adiponectin (15,20,21). As shown in Fig. 1C, DPP4 release is significantly upregulated by TNF-α and insulin. In addition to adipocytes, adipose tissue-derived macrophages release measurable amounts of DPP4 (Fig. 1D). However, this is only one third compared with adipocytes, pointing to a major contribution of adipocytes to DPP4 output from adipose tissue.
Soluble DPP4 exerts direct effects on fat and muscle cells
The soluble form of DPP4 may bind to the extracellular matrix (22) and affect a variety of cells, yet this has not been investigated so far. To assess potential direct effects of soluble DPP4 on peripheral cells, we studied insulin signaling in adipocytes and skeletal muscle cells. DPP4 treatment of human adipocytes results in a dose-dependent decrease in insulin-stimulated Akt phosphorylation, which reached significance using a dose of 200 ng/mL (Fig. 2A). This demonstrates an autocrine effect of DPP4 on adipocytes. It should be noted that circulating DPP4 concentrations were found in the range of 200 to 600 ng/mL in healthy patients. The effect of DPP4 on insulin-stimulated Akt phosphorylation can be completely blocked by a specific DPP4 inhibitor (Fig. 2B). Validation experiments using this compound proved inhibition of DPP4 in vitro, which remained unaltered for a period of at least 8 h (data not shown). Similar to adipocytes, DPP4 also induces IR in skeletal muscle cells at the level of Akt phosphorylation in a dose-dependent way but less prominent compared with adipocytes (Fig. 2C and D). To prove whether DPP4 has a functional impact not only on insulin signaling, we determined DPP4-stimulated proliferation and insulin signaling in primary human smooth muscle cells. In addition to the induction of IR at the level of Akt in this cell type, DPP4 induced a 1.6-fold increase in cell proliferation that can be completely blocked by the DPP4 inhibitor (Fig. 3A–C).
DPP4 is elevated in serum of obese patients and correlates with various anthropometric and clinical parameters (clinical study 1)
Measuring DPP4 in serum from age-matched lean and morbidly obese subjects (patient characteristics in Supplementary Table 1) revealed that obese subjects are characterized by significantly increased DPP4 concentrations (Fig. 4A). DPP4 expression in adipose tissue biopsies from the same patients revealed that DPP4 protein expression is regulated by both the fatness of the individual and the adipose tissue depot (Fig. 4B). Although there is only a trend for higher DPP4 expression in visceral fat of lean subjects, obese patients are characterized by significantly higher DPP4 in visceral adipose tissue compared with subcutaneous adipose tissue. Furthermore, expression of DPP4 in both depots is significantly higher in obese subjects compared with lean subjects. DPP4 levels positively correlate with BMI, the size of subcutaneous and visceral adipocytes, insulin, and leptin, whereas a negative correlation with age and adiponectin could be found (Fig. 5A–G). Adjusting DPP4 for age has no impact on these correlations. However, when adjusted for BMI, DPP4 serum concentrations significantly correlate only with the size of subcutaneous adipocytes (P = 0.04, r = 0.32), pointing to a close relation between the size of adipocytes and the release of this adipokine.
DPP4 is released from subcutaneous adipose tissue in vitro (clinical study 2)
We investigated lean and obese subjects after weight reduction and analyzed the release of DPP4 from whole adipose tissue. Adipocytes from lean subjects were significantly smaller than those from obese patients (Fig. 6A). Surgery-induced weight loss reduced the average size of adipocytes below the size from lean subjects. DPP4 release is significantly increased from adipose tissue of obese subjects compared with lean subjects (Fig. 6B), whereas weight reduction by bariatric surgery normalized the DPP4 release to the lean level. This was paralleled by a significant reduction in the circulating DPP4 level, supporting the notion that adipose tissue is an important source of serum DPP4 (Fig. 6C). In the group of lean and obese subjects, DPP4 release from adipose tissue significantly correlates with BMI, waist circumference, percent body fat, triglycerides, HOMA, adipocyte volume, and leptin, whereas the correlation is negative with HDL-cholesterol (Fig. 6D–K). All of these factors are denominators of the metabolic syndrome. It is noteworthy that leptin shows similar correlations with the above mentioned parameters, with the exception of triglycerides, for which no correlation could be found. Notably, the release of DPP4 from adipose tissue correlates with many parameters that correlate with circulating DPP4 concentrations. There is also a strong correlation between adipose secretion of leptin and DPP4 (Fig. 6K).
DPP4 serum concentrations and release from adipose tissue are significantly related to the metabolic syndrome
In both obese patient groups providing data for circulating DPP4 levels and DPP4 release from adipose tissue explants, the respective concentrations of DPP4 are significantly increased in subjects with a risk score for the metabolic syndrome of ≥3, as calculated according to the Adult Treatment Panel-III guidelines (Fig. 7A and B). By performing the same analysis for the circulating levels of leptin, monocyte chemotactic protein-1, RANTES (regulated upon activation, normal T cell expressed and secreted), plasminogen activator inhibitor-1, chemerin, and high-sensitivity C-reactive protein, we did not find any such relationship with the metabolic syndrome (data not shown). In contrast, adiponectin serum levels were significantly decreased in patients with the metabolic syndrome (data not shown). Including the lean subjects in this type of analysis does not change the outcome of this analysis, and it should be noted that the relationship of DPP4 with the risk score for the metabolic syndrome in the obese subjects is independent from BMI.
Our proteomics approach identified DPP4 as a novel adipokine released by fully differentiated human adipocytes. This was confirmed by Western blot, ELISA, and determination of enzymatic activity. DPP4 release increased substantially on fat cell differentiation, and comparison with preadipocytes and adipose tissue macrophages showed that adipocytes most likely represent the major source of DPP4 released from the intact organ to the circulation. DPP4 is a multifunctional, type II integral membrane glycoprotein exhibiting ubiquitous expression, including adipose tissue (23), being highly abundant in the kidney, on T lymphocytes and endothelial cells (22). DPP4 is certainly different from many other adipokines in that 1) the protein is not secreted but released from the plasma membrane as soluble DPP4 subsequent to proteolytic cleavage (24), 2) DPP4 exerts dual functions both as a regulatory protease and a binding protein, and 3) this protein is already an established target for treatment of type 2 diabetes (8), supporting our notion that DPP4 may potentially link adipose tissue to type 2 diabetes and the metabolic syndrome. Regulators of DPP4 release are presently unknown, but we show that both insulin and TNF-α augment the shedding of soluble DPP4 by ∼50% despite an unaltered expression. Thus, factors related to IR and adipose tissue inflammation enhance the release of this novel adipokine from the fat cell. In addition to the endocrine effects of DPP4 released to the circulation, both cell surface resident and soluble DPP4 may have multiple autocrine and paracrine functional implications for adipose tissue physiology. First, DPP4 recruits adenosine deaminase to the cell surface (25), which may modulate the well established antilipolytic effects of adenosine. Second, DPP4 is a strong inhibitor of the antilipolytic activity of neuropeptide Y (23), which is one of the best peptide substrates of the enzyme (26). Therefore, enhanced abundance of both resident and soluble DPP4 within adipose tissue of obese subjects may substantially augment the lipolytic activity of enlarged adipocytes. Finally, DPP4 inactivates or alters the specificity of many chemokines, including RANTES, eotaxin, macrophage-derived chemokine, stromal-derived factor-1, and many others (22), making it likely that DPP4 plays a yet undefined functional role in the intraorgan cross-talk among macrophages, adipocytes, and other components of the stroma-vascular fraction.
So far, the direct effects of soluble DPP4 on isolated cells have not been investigated, although it binds to the extracellular matrix and may exert signaling functions (22). We demonstrate for the first time that DPP4 consistently impairs insulin signaling at the level of Akt in three different primary cell types, namely, adipocytes, skeletal muscle, and smooth muscle cells. Enzymatic activity of DPP4 seems to be involved in this process, but DPP4 inhibitors may also affect the binding properties of sDPP4 to a putative receptor. This issue is currently under investigation in our laboratory. It may be speculated that DPP4 exerts an autocrine action on adipocytes, which may be of particular interest for perivascular fat, where DPP4 may also act in a paracrine/endocrine fashion on the vascular wall. DPP4 induces proliferation of human vascular cells in parallel to an impairment of insulin signaling, suggesting a potential role in obesity-associated vascular complications. In this study, we used DPP4 concentrations that match circulating levels that were measured in both lean and obese subjects. Because obese patients are characterized by significantly increased circulating DPP4, it may be speculated that DPP4 may interfere with insulin sensitivity not only in adipose tissue but also in other insulin-sensitive peripheral organs. This would substantially extend the current view of DPP4 as a target for treatment of type 2 diabetes. Future work will be needed to address the mechanism and the functional role of these effects in the pathogenesis of IR and obesity-associated complications.
Serum DPP4 is altered in many pathophysiologic conditions, such as different types of cancer, allergic asthma, or hepatitis C (10). To the best of our knowledge, this is the first study to analyze circulating DPP4 in the context of obesity and adipose tissue. Morbidly obese men are characterized by elevated DPP4 levels compared with lean controls. DPP4 serum concentrations are significantly correlated with the BMI, the size of adipocytes in subcutaneous and visceral fat, and the adipocyte hormones adiponectin (negatively) and leptin, showing that DPP4 is related to not only increased body weight but also other important parameters of adipose tissue in particular. DPP4 is negatively associated with age, but all of the above mentioned parameters are still significantly correlated with DPP4, even after adjustment for age. In a different manner, BMI adjustment causes the disappearance of most of these correlations, with the exception of the size of subcutaneous adipocytes. In addition to circulating DPP4, the protein expression of this adipokine is significantly different not only between lean and obese subjects but also between their fat depots. Former studies report contradicting data, describing both decreased and increased mRNA expression of DPP4 in adipose tissue of obese men (23,27). We now clearly demonstrate at the protein level that obesity leads to a prominent induction of DPP4 abundance in both subcutaneous and visceral adipose tissue and that the visceral fat exhibits the highest DPP4 level in obese subjects. Therefore, we conclude that enlargement of visceral adipocytes in obesity may substantially contribute to the augmented level of circulating DPP4 in obese patients. It is noteworthy that we measured DPP4 serum concentration and not its activity. However, in additional experiments, other samples from the same patients were used to determine DPP4 activity that is significantly correlated with circulating DPP4 levels (data not shown). Thus, DPP4 activity is also significantly increased in obese compared with lean subjects.
DPP4 expression in adipose tissue is increased in obese compared with lean individuals, a fact that is reflected by an increased release of DPP4 from adipose tissue explants of obese patients compared with lean controls. Similar to circulating DPP4, its release from adipose tissue correlates with various classic markers for the metabolic syndrome, namely, BMI, waist circumference and plasma triglycerides, and HOMA as an index of IR, as well as with fat cell volume and the adipokine leptin. In addition, DPP4 release can be reversed to normal levels by surgery-induced weight loss, which is also reflected by DPP4 being significantly reduced in serum of these patients. With the exception of one study reporting on DPP4 levels in obese children before and after weight loss (28), this is the first description of significantly decreased DPP4 levels after weight loss induced by obesity surgery in adults. Thus, in obesity, both circulating levels of DPP4 and DPP4 release by adipose tissue are increased but can be reduced to control levels by substantial weight loss.
Both circulating DPP4 and DPP4 release by adipose tissue correlate strongly with the metabolic syndrome. Thus, DPP4 may be of relevance as a novel biomarker of the metabolic syndrome and for detection of obese subjects at high risk for obesity-associated complications. Future studies are needed to address this important issue and to define the molecular pathways that link adipose DPP4 to the metabolic syndrome and type 2 diabetes. An adipose-specific knockout of DPP4 would be required to prove a causal role of this protein, and this mouse model is currently under development in our laboratory. However, several lines of evidence support our notion that the novel adipokine links obesity to the metabolic syndrome. First, DPP4 impairs the function of the incretin system, which is of key importance for glucose homeostasis (29). Incretin-based therapies are known to preserve β-cell function and to exert salutary effects on blood pressure and lipid profile (30). Second, DPP4 inhibitors are well known to improve glucose tolerance in animal models of obesity (31). More important, chronic DPP4 inhibition in ZDF rats was shown to delay the onset of type 2 diabetes (31). Finally, preclinical data suggest that GLP-1 is cardioprotective (32), and DPP4 inhibition was shown to improve cardiovascular outcomes in rodents (33). Our data strongly support the current view (20) that adipocytes and specifically adipose tissue play a major, most likely causative role in the pathogenesis of metabolic diseases.
In summary, we showed that DPP4 is a novel adipokine that is substantially overexpressed in visceral fat from obese subjects and exhibits an augmented release in obesity. Soluble DPP4 exerts autocrine and paracrine effects and impairs insulin signaling. We further observe a tight correlation of DPP4 release to adipocyte cell size, and plasma levels of DPP4 strongly correlate with the risk of having the metabolic syndrome. Therefore, we suggest that DPP4 is a novel biomarker and a potential link between obesity and the metabolic syndrome.
This work was supported by the Bundesministerium für Gesundheit, the Ministerium für Innovation, Wissenschaft und Forschung NRW, Deutsche Forschungsgemeinschaft (SE 1922/2-1), Commission of the European Communities (Collaborative Project ADAPT, contract number HEALTH-F2-2008-201100, Integrated Project HEPADIP, contract number LSHM-CT-2005-018734), EU COST Action BM0602, the Swedish Research Council (K2008-54X-01034-42-4 and 2007-2489), the Swedish Diabetes Association, the Swedish Heart and Lung Association, the Diabetes Program at Karolinska Institutet, and the Novo Nordisk Foundation. No other potential conflicts of interest relevant to this article were reported.
D.L., S.F., N.W., and S.H. researched data; S.L. contributed to discussion and reviewed and edited the manuscript; D.M.O. contributed to discussion and reviewed and edited the manuscript; K.E. reviewed and edited the manuscript; J.M.K., M.R., S.M., and F.-G.H. researched data; J.R. researched data and reviewed and edited the manuscript; P.A. researched data and contributed to discussion; H.S. researched data and wrote the manuscript; and J.E. wrote the manuscript.
The authors thank Prof. Jutta Liebau and her team, Department of Plastic Surgery, Florence-Nightingale-Hospital Düsseldorf, for support in obtaining adipose tissue samples. The technical assistance of Andrea Cramer, Angelika Horrighs, Birgit Knobloch, and Kerstin Wåhlén and the secretarial assistance of Birgit Hurow (Paul-Langerhans-Group, German Diabetes Center) are acknowledged.
This article contains Supplementary Data online at http://diabetes.diabetesjournals.org/lookup/suppl/doi:10.2337/db10-1707/-/DC1.
- Received December 8, 2010.
- Accepted April 2, 2011.
- © 2011 by the American Diabetes Association.
Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.