Advanced glycation end products evoke endothelial cell damage by stimulating soluble dipeptidyl peptidase-4 production and its interaction with mannose 6-phosphate/insulin-like growth factor II receptor

An inhibitor of DPP-4, linagliptin was generously gifted from Boehringer Ingelheim (Ingelheim, Germany). Bovine serum albumin (BSA) (essentially fatty acid free and essentially globulin free, lyophilized powder), D-Mannose-6-phosphate (M6P) and N-acetylcysteine (NAC) were purchased from Sigma (St. Louis, MO, USA). D-glyceraldehyde from Nakalai Tesque (Kyoto, Japan). Recombinant human DPP-4 from R&D systems (Minneapolis, MN, USA). Hydrogen peroxide (H₂O₂) from Wako Pure Chemical Industries Ltd. (Osaka, Japan). Antibody (Ab) directed against human M6P/insulin-like growth factor II receptor (IGF-IIR) (M6P/IGF-IIR-Ab) and DPP-4 from Santa Cruz Biotechnology Inc. (Delaware, CA, USA).

HUVECs were cultured in endothelial basal medium supplemented with 2% fetal bovine serum, 0.4% bovine brain extracts, 10 ng/ml human epidermal growth factor and 1 μg/ml hydrocortisone according to the supplier’s instructions (Clonetics Corp., San Diego, CA). DPP-4 or AGE treatment was carried out in a medium lacking epidermal growth factor and hydrocortisone.

HUVEC were treated with or without the indicated concentrations of DPP-4, 100 μg/ml AGE-BSA or 100 μg/ml non-glycated BSA in the presence or absence of 50 μM M6P, 5 μg/ml M6P/IGF-IIR-Ab, 10 nM or 0.5 μM linagliptin for 4 hr, and then the cells were incubated with phenol red free Dulbecco's Modified Eagle Medium containing 3 μM DHE (Molecular Probes Inc., Eugene, OR, USA). After 15 minutes, the cells were imaged under a laser-scanning confocal microscope. Superoxide generation was evaluated by intensity of DHE staining. The intensity was analyzed by microcomputer-assisted NIH image.

Recombinant human IGF-IIR (100 μg/ml, R&D system) was immobilized via the amino groups to CM5 sensor chip (GE Healthcare, Buckinghamshire, UK) with the aid of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and N-hydroxysuccinimide. For affinity measurements, the association and dissociation phases were monitored in a BIAcore 1000 (GE Healthcare). Recombinant human DPP-4 was injected into the flow cell at concentrations of 0.1 and 0.3 μM at a flow rate of 10 μl/min at 25°C. The sensor chip was regenerated with pulses of 20 mM Tris–HCl buffer (pH 8.0) containing 6 M urea to the baseline level, followed by an extensive washing with the running buffer. Control experiments were performed with IGF-IIR-free channel on the same sensor chip. From the assay curves obtained, the control signals, reflecting the bulk effect of buffer, were subtracted using BIA-evaluation 4.1 software (GE Healthcare). Equilibrium dissociation constant (K_D) was determined using the equation for 1:1 Langmuir binding.

HUVEC were treated with or without the indicated concentrations of DPP-4, 100 μg/ml AGE-BSA or 100 μg/ml non-glycated BSA in the presence or absence of 10 nM or 0.5 μM linagliptin for 4 hr. Then total RNA was extracted with RNAqueous-4PCR kit (Ambion Inc., Austin, TX, USA) according to the manufacturer’s instructions. Quantitative real-time RT-PCR was performed using Assay-on-Demand and TaqMan 5 fluorogenic nuclease chemistry (Applied Biosystems, Foster city, CA, USA) according to the supplier’s recommendation. IDs of primers for human RAGE, ICAM-1, PAI-1, β-actin and 18S gene were Hs00153957_m1, Hs00164932_m1, Hs01126606_m1, Hs99999903_m1, and Hs99999901_s1, respectively.

AGE-BSA was prepared as described previously [15]. In brief, BSA (25 mg/ml) was incubated under sterile conditions with 0.1 M glyceraldehyde in 0.2 M NaPO₄ buffer (pH 7.4) for 7 days. Then unincorporated sugars were removed by PD-10 column chromatography and dialysis against phosphate-buffered saline. Control non-glycated BSA was incubated in the same conditions except for the absence of reducing sugars. Preparations were tested for endotoxin using Endospecy ES-20S system (Seikagaku Co., Tokyo, Japan); no endotoxin was detectable.

Ab directed against human RAGE was prepared as described previously [16].

HUVECs were treated with or without 100 μg/ml AGE-BSA, 100 μg/ml non-glycated BSA or the indicated concentrations of H₂O₂ in the presence or absence of 1 mM NAC, 5 μg/ml RAGE-Ab or 10 nM linagliptin for 24 hr. Conditioned medium were collected and concentrated 20-fold using an Amicon ultrafiltration system (5000-kDa cutoff, Merck Millipore, Darmstadt, Germany) according to the method described previously [16]. Then 20 μg proteins were separated by SDS-PAGE and transferred to polyvinylidene difluoride membranes as described previously [17]. Membranes were probed with Ab directed against human DPP-4, and then immune complexes were visualized with an enhanced chemiluminescence detection system (Amersham Bioscience, Buckinghamshire, United Kingdom).

Unless otherwise indicated, all values were presented as means ± SE from at least 3 independent experiments. Statistical analyses were performed by one-way ANOVA followed by the Scheffe F test for multiple comparisons, and p < 0.05 was considered statistically significant. All statistical analyses were performed with the use of the PASW Statistics system (version 18.0; IBM Corporation, New York, NY, USA).

M6P/IGF-IIR has been shown to work as a receptor for DPP-4 in HUVECs and mediates its biological action, resultantly promoting transendothelial T cell migration, and an effect requires the enzymatic activity of DPP-4 [18]. In this study, we found for the first time that blocking the interaction of DPP-4 with M6P/IGF-IIR by the addition of excess amount of free M6P or M6P/IGF-IIR-Ab completely inhibited the DPP-4-induced increase in superoxide generation in HUVECs. Further, SPR analysis revealed that DPP-4 actually bound to M6P/IGF-IIR, and an inhibitor of DPP-4, linagliptin completely prevented the ROS generation and up-regulation of RAGE mRNA levels in DPP-4-exposed HUVECs. Since we have previously shown that AGEs stimulate RAGE gene expression in ECs via ROS generation [15], our present observations suggest that DPP-4 could increase ROS generation and subsequently RAGE gene overexpression in HUVECs through the interaction with M6P/IGF-IIR, whose ability is totally dependent on its intrinsic DPP-4 enzymatic activity. AGEs have been shown to impair the migration, adhesion and secretion potentials of late endothelial progenitor cells [19, 20]. Further, AGE-RAGE interaction causes inflammation and thrombogenesis in diabetic vessels [21, 22]. Therefore, given the atherosclerosis-promoting properties of AGE-RAGE axis, although the reason why DPP-4 caused vascular damage in diabetes remains unclear, DPP-4 itself might be involved in diabetic vascular injury. DPP-4 has been reported to not only stimulate proliferation of human coronary artery smooth muscle cells [23], but also contribute to monocyte migration, macrophage-mediated inflammatory reactions and tissue remodeling [24, 25], thus supporting the speculation that DPP-4 itself might work as a risk factor for atherosclerosis.

In this study, AGEs stimulated the release of DPP-4 from HUVECs, which was significantly inhibited by the treatment with an anti-oxidant, NAC, RAGE-Ab, or linagliptin. Moreover, H₂O₂ dose-dependently increased the production of soluble DPP-4 by HUVECs. So, the AGE-RAGE-induced ROS generation could be involved in soluble DPP-4 generation by HUVECs. The present findings have extended our previous observations [17] showing that serum levels of AGEs were independently correlated with circulating DPP-4 values in 432 consecutive outpatients and that AGEs significantly increase soluble DPP-4 release from cultured proximal tubular cells, one of the major cell types that expressed DPP-4 in humans [26]. Since we previously reported that AGEs at 100 μg/ml for 4 hr did not affect DPP-4 mRNA levels in HUVECs [27], the AGE-RAGE interaction might promote the proteolytic cleavage of membrane-bound DPP-4 from HUVECs via superoxide generation. Serum levels of AGEs are positively rather than inversely associated with soluble form of RAGE (sRAGE) (endogenous secretory RAGE plus cleaved RAGE) in both diabetic and non-diabetic subjects [28, 29]. Therefore, although exogenously administered sRAGE was shown to block the harmful effects of AGEs in animals by acting as a decoy receptor, it is questionable that sRAGE in humans could also exert the same biological effect, because its serum concentration is 1000 times lower than needed for efficiently capturing and eliminating the circulating AGEs [30]. Moreover, engagement of RAGE with its ligand has been shown to promote the RAGE shedding [30, 31]. These findings suggest that sRAGE level could reflect tissue RAGE expression and that AGEs might enhance the cleavage of DPP-4 from the cell membrane. Given the facts that serum DPP-4 activity is largely associated with circulating DPP-4 levels [10, 32] and that 20% of incretins derived from gastrointestinal tract are still alive in the blood pool [33, 34], cumulative hyperglycemia and resultant AGE accumulation might impair the incretins’ effects via elevation of circulating DPP-4 levels, further deteriorating glycemic control and thereby forming a vicious cycle in diabetic subjects. This scenario could support the clinical relevance of blockade of the pathological crosstalk between AGE-RAGE axis and DPP-4 by linagliptin in the treatment with type 2 diabetes.

In the present study, we found that linagliptin significantly inhibited the AGE-induced ROS generation, RAGE, ICAM-1 and PAI-1 gene expression in HUVECs. AGEs are reported to up-regulate RAGE gene expression in a variety of cells via ROS generation and induce activation of redox-sensitive transcriptional factor, NF-kB and subsequent ICAM-1 and PAI-1 gene induction [7, 15, 31, 35‐37]. Therefore, the AGE-RAGE-induced oxidative stress generation could further potentiate the harmful effects of AGEs via RAGE overexpression. So, linagliptin might inhibit the AGE-evoked inflammatory and thrombogenic responses in HUVECs by blocking the positive feedback loops between ROS generation and RAGE gene up-regulation. In this study, we could not clarify the mechanism by which linagliptin inhibited the AGE-induced ROS generation in HUVECs. However, we have previously shown that GLP-1 and GIP protect against AGE-induced HUVEC damage via anti-oxidative properties through the elevation of cyclic AMP, whose effect is augmented by the addition of DPP-4 inhibitor [27, 38, 39]. Since AGE-RAGE axis evokes ROS generation in ECs via NADPH oxidase activity, which is blocked by cAMP-elevating agents [6, 7, 15, 40], linagliptin could enhance the beneficial effects of incretins on AGE-exposed HUVECs by inhibiting NADPH oxidase activity. Furthermore, we have recently found that linagliptin contains xanthine scaffold structure, which could inhibit xanthine oxidase activity in vitro[41]. The anti-oxidative unique properties of this drug might also be involved in the blockade of vicious cycle between ROS generation and RAGE gene induction. It is unlikely that linagliptin directly inhibited the AGE-RAGE interaction because highly sensitive 27-MHz quartz crystal microbalance analysis (Affinix Q; Initium, Tokyo, Japan) revealed that linagliptin can not bind to AGEs in vitro (data not shown).

One early phase of atherosclerosis involves the recruitment and firm adhesion of inflammatory cells to ECs, whose process is mediated by adhesion molecules such as ICAM-1 [42, 43]. Further, attenuated fibrinolytic activity due to increased PAI-1 levels is prevalent in diabetic patients, thus contributing to the increased risk of atherothrombosis in these subjects [37, 44, 45]. Linagliptin may be a promising strategy for not only ameliorating hyperglycemia in type 2 diabetic patients, but also protecting against vascular injury by suppressing ICAM-1 and PAI-1 expression through blockade of the deleterious effects of AGE-RAGE axis partly via inhibition of DPP-4 and M6P/IGF-IIR interaction. In pre-specified meta-analysis of cardiovascular events in linagliptin or comparator-treated patients with type 2 diabetes mellitus, the hazard ratio for a composite of cardiovascular death, stroke, myocardial infarction, and hospitalization for unstable angina showed significantly lower risk with linagliptin than comparator [46]. Moreover, we have very recently found that DPP-4 inhibitor alogliptin treatment blocks the AGE-RAGE axis and resultantly reduces albuminuria in type 2 diabetes patients [47]. Fluorescent AGE levels have also been shown to be an independent marker of post-infarction heart failure development risk [48]. These data reinforce the important clinical implications of the present findings of linagliptin.

The peak plasma concentration of linagliptin after administration of single oral dose of 5 mg is reported to be about 10 nM [49]. So, the concentration of linagliptin having beneficial effects on HUVECs used in the present experiments (10 nM) may also be comparable to the therapeutic level which is achieved in the treatment for patients with type 2 diabetes.

Our study has several limitations that should be noted. First, we did not examine here the effect of M6P/IGF-IIR-Ab on the increase in ROS generation induced by AGEs or the increase in RAGE gene expression induced by DPP-4 and AGEs. Second, although mRNA levels of DPP-4 were not changed by the treatment with AGEs, the effect of linagliptin on membrane DPP-4 expression in AGE-exposed HUVECs remains unknown. Additional experiments would strengthen the present findings.