Research | Open | Published:
Vildagliptin ameliorates pulmonary fibrosis in lipopolysaccharide-induced lung injury by inhibiting endothelial-to-mesenchymal transition
Respiratory Researchvolume 18, Article number: 177 (2017)
Pulmonary fibrosis is a late manifestation of acute respiratory distress syndrome (ARDS). Sepsis is a major cause of ARDS, and its pathogenesis includes endotoxin-induced vascular injury. Recently, endothelial-to-mesenchymal transition (EndMT) was shown to play an important role in pulmonary fibrosis. On the other hand, dipeptidyl peptidase (DPP)-4 was reported to improve vascular dysfunction in an experimental sepsis model, although whether DPP-4 affects EndMT and fibrosis initiation during lipopolysaccharide (LPS)-induced lung injury is unclear. The aim of this study was to investigate the anti-EndMT effects of the DPP-4 inhibitor vildagliptin in pulmonary fibrosis after systemic endotoxemic injury.
A septic lung injury model was established by intraperitoneal injection of lipopolysaccharide (LPS) in eight-week-old male mice (5 mg/kg for five consecutive days). The mice were then treated with vehicle or vildagliptin (intraperitoneally, 10 mg/kg, once daily for 14 consecutive days from 1 day before the first administration of LPS.). Flow cytometry, immunohistochemical staining, and quantitative polymerase chain reaction (qPCR) analysis was used to assess cell dynamics and EndMT function in lung samples from the mice.
Lung tissue samples from treated mice revealed obvious inflammatory reactions and typical interstitial fibrosis 2 days and 28 days after LPS challenge. Quantitative flow cytometric analysis showed that the number of pulmonary vascular endothelial cells (PVECs) expressing alpha-smooth muscle actin (α-SMA) or S100 calcium-binding protein A4 (S100A4) increased 28 days after LPS challenge. Similar increases in expression were also confirmed by qPCR of mRNA from isolated PVECs. EndMT cells had higher proliferative activity and migration activity than mesenchymal cells. All of these changes were alleviated by intraperitoneal injection of vildagliptin. Interestingly, vildagliptin and linagliptin significantly attenuated EndMT in the absence of immune cells or GLP-1.
Inhibiting DPP-4 signaling by vildagliptin could ameliorate pulmonary fibrosis by downregulating EndMT in systemic LPS-induced lung injury.
The morbidity and mortality of acute respiratory distress syndrome (ARDS) is especially high when it leads to persistent intra-alveolar and interstitial fibrosis [1, 2]. The most common cause of ARDS is sepsis that involves direct or indirect interactions between endotoxins and pulmonary vascular endothelial cells (PVECs).
Our recent study showed that one of the innate survival strategies for non-apoptotic injured PVECs is endothelial-to-mesenchymal transition (EndMT) , which is a process wherein endothelial cells lose an endothelial cell phenotype and acquire a mesenchymal cell phenotype . There are many pathways, such as those that include the transforming growth factor β (TGFβ) superfamily, through which EndMT is induced [4, 5].
We recently reported that transient EndMT was observed in mice with septic acute lung injury (ALI) that can be repaired . LPS-induced EndMT was reported to be dependent on ROS levels in vitro , and in vivo . In the repairable ALI mouse model, transient EndMT cells have a progenitor cell-like phenotype that could be involved in endothelial repair after pulmonary vascular injury . Some of pulmonary microvascular endothelial cells transform into mesenchymal phenotype with retaining reversibility to their original phenotype when endotoxin stimulation is transient. However, it is unclear whether continuous or intermittent endotoxin exposure promotes complete EndMT and pulmonary fibrosis.
Indeed, numerous studies found that endothelial cells are one source of fibroblasts/myofibroblasts in fibrotic diseases [7,8,9]. The etiology of fibrotic diseases can vary widely. Given that one of the main initial targets of endotoxins is vascular endothelial cells especially in case of ARDS from extra-pulmonary origin [6, 10], EndMT could thus be closely involved in the pathogenesis of pulmonary fibrosis after systemic endotoxemic injury.
CD26/dipeptidyl peptidase 4 (DPP-4) is broadly expressed by a variety of cell types in the lung, including capillary endothelial cells . DPP-4 inhibitors are widely used glucose-lowering drug that inhibit the breakdown of the incretin hormone glucagon-like peptide-1 (GLP-1) . They have recently gathered increasing interest since they might have beneficial effects on cardiovascular diseases [13,14,15]. Although most of the previous reports explained their vascular protective effects by the upregulation of GLP-1 and lowering blood glucose level [16, 17], it was also reported that they could act in some part not through the breakdown of GLP-1. Kohashi et al. elegantly revealed that DPP-4 inhibitor but not GLP-1 reduced incidence of angiotensin II-induced abdominal aortic aneurysm in ApoE −/− mice . In addition, DPP-4 inhibition was reported to prevent systemic inflammation, vascular dysfunction and end organ damage in endotoxemic conditions , and ameliorate kidney fibrosis in diabetic mice . Thus, it has been revealed that DPP-4 inhibitors have various effects without increasing insulin secreting property from pancreas β-cell or GLP-1.
Based on these findings, we hypothesize that EndMT is involved in the pathogenesis of pulmonary fibrosis after systemic endotoxemic injury, which can be attenuated by the DPP-4 inhibitor vildagliptin. In the present study, we examined whether intermittent LPS exposure leads to pulmonary fibrosis via EndMT. We also evaluated the therapeutic potential of vildagliptin for inhibiting post-ALI pulmonary fibrosis partly via GLP-1-independent antioxidant pathway.
Mouse model of pulmonary fibrosis after systemic endotoxemic injury
We modified the experimental protocol for induction of pulmonary fibrosis in mice by intermittent intraperitoneal lipopolysaccharide (LPS) injection . Seven- to eight-week-old male C57BL/6 mice (Clea Japan, Tokyo, Japan) received intraperitoneal administration of 5 mg/kg body weight LPS for five consecutive days. The LPS was derived from Escherichia coli (O55:B5 Sigma, St. Louis, MO) and dissolved in PBS. For treatment in vivo with vildagliptin, mice were given once daily doses of either 10 mg/kg vildagliptin (Santa Cruz Biotechnology, Dallas, TX) or saline vehicle delivered by intraperitoneal injection for 14 consecutive days from 1 day before the first administration of LPS. At 14 days and 28 days after starting LPS injection, mice were anaesthetized, and lung tissues were quickly removed and processed as described below. All animal experiments were conducted under protocols approved by the Chiba University Institutional Review Board for animal experiments.
Lung histological analyses
Resected lungs were formalin fixed and embedded in paraffin. Lung sections (2 μm) were deparaffinized in xylene, hydrated using ethanol, and stained with Elastica van Gieson (EVG) stain using standard protocols for morphological analyses. The pulmonary fibrosis severity was semi-quantitatively assessed according to the method proposed by Ashcroft .
Lungs were embedded in Tissue-Tek®,O.C.T. Compound (SAKURA Finetek, Tokyo) and frozen in liquid nitrogen for preparation of cryosections. Frozen lung tissues were cut into 6 μm thick sections, immunostained and visualized by confocal microscopy (Fluoview FV 10i, Olympus, Tokyo). The sections were fixed in acetone for 10 min, blocked with Block Ace (Dainippon Sumitomo Pharma, Tokyo) for 10 min, and incubated with the primary and secondary antibodies for 60–120 min. The following antibodies were used for immunostaining: anti-CD31-Alexa488 (BioLegend, San Diego, CA), anti-CD45-Alexa647 (BioLegend), anti-CD26 (R&D Systems, Minneapolis, MN), anti-α-SMA (Thermo Scientific, Waltham, MA), and anti-S100 calcium-binding protein A4 (S100A4) (Abcam, Cambridge, UK).
Human pulmonary vascular endothelial cell injury model
Human lung microvascular endothelial cells (HMVEC-L) were purchased from Clonetics (Walkersville, MD) and cultured in endothelial cell basal medium-2 (EBM-2, Lonza, Walkersville, MD) supplemented with 10% fetal bovine serum and endothelial cell growth medium 2 (EGM-2 SingleQuots, Invitrogen, Carlsbad, CA). All cells were maintained at 37 °C in a 5% CO2 humidified incubator. Cells were cultured to 90% confluence and transitioned to starvation medium that included EBM-2 supplemented with 1% fetal bovine serum, 0.1% gentamicin sulfate and amphotericin-B, heparin, and ascorbic acid for 24 h. Cells were exposed to vehicle (PBS) or LPS (20 μg/ml) with or without DPP-4 inhibitor (Vildagliptin 10 nM. Linagliptin 100 nM.) in fresh starvation medium at 37 °C for 96 h.
Single cell suspension
At the time of harvest, mouse lungs were perfused with 30 ml PBS containing 10 U/ml heparin (Novo-Heparin, Mochida, Tokyo) from the right ventricle until there was no visible blood. The tissue was then minced and placed in an enzyme cocktail consisting of DMEM (Sigma), 1% BSA (Wako, Osaka, Japan), 2 mg/ml collagenase (Wako), 100 μg/ml DNase (Wako), and 2.5 mg Dispase II (Roche Diagnostics GmbH, Mannheim, Germany) at 37 °C for 60 min before the tissue was passed through a nylon cell strainer with a 100 μm mesh size.
Flow cytometry (FCM) of lung cells
Mouse lung cells were pretreated with anti-CD16/32 antibody (BioLegend) to block Fc receptors, and then incubated with specific antibodies at 4 °C in the dark. The following antibodies were used for cell surface staining: anti-CD31-PE/Cy7 (BioLegend), anti-CD45-Alexa700 (BioLegend) and anti-CD26-PE (BioLegend). To measure α-SMA and S100A4 levels, after surface staining the cells were incubated with anti-α-SMA (Thermo Scientific) and anti-S100A4 (Abcam) for 35 min at 22 °C. Cells were then incubated for 25 min at 22 °C with donkey anti-rabbit IgG-Alexa 488 (IgG; H + L) (Life Technologies) as a secondary antibody.
HMVEC-Ls were pretreated with anti-CD16/32 antibody and then incubated with anti-CD31, −CD45, and -α-SMA. Cell fluorescence was measured using a FACSCantoTM II instrument (Becton Dickinson, San Jose, CA) and the output was analyzed with FlowJo software (Tree Star, San Carlos, CA).
Isolation of mouse PVECs and mouse mesenchymal cells
Mouse PVECs were defined as CD31+/CD45−/CD326− cells, and mouse mesenchymal cells were defined as CD31−/CD45−/CD326− cells. Each cell type was sorted using the BD FACS Aria II cell sorter as previously reported . Propidium iodide (0.5 μg/ml) (Thermo Scientific) staining was used to exclude dead cells.
Fluorescent immunocytochemistry (ICC)
Isolated mouse PVECs were fixed in a 1:1 mixture of methanol and acetone for 2 min followed by blocking with normal goat serum for 30 min as per our previous report . The cells were incubated with primary antibodies (anti-α-SMA and anti-CD31) for 1 h at room temperature, and then with secondary antibodies for 1 h at room temperature. Finally, Hoechst 34,580 (Sigma) was used to identify cell nuclei, and the cells were examined by confocal microscopy (Fluoview FV 10i, Olympus). HMVEC-Ls cultured with or without LPS for 96 h were immunostained using the same method.
Total RNA from CD31+/CD45−/CD326− cells and CD31−/CD45−/CD326− cells were isolated with Nucleo Spin RNA XS (MACHEREY NAGEL GmbH & Co. KG, Düren, Germany) according to the manufacturer’s instructions. RNA was subjected to RT-PCR with SuperScript VILO (Life Technologies) according to the manufacturer’s protocol and single stranded cDNA was synthesized. The resulting cDNA samples were subjected to PCR for amplification using an ABI Prism 7300 Sequence Detection System (Applied Biosystems, Carlsbad, CA). Specific primers and probes were designed using Web-based software from the Universal ProbeLibrary Assay Design Center (Roche Applied Science). The Ct value for each sample was normalized with respect to Hprt1 as an endogenous control gene and the relative expression level was calculated using the 2-ΔΔCt method. The details of the primer sequences are described in Additional file 1.
Reactive oxygen species (ROS) generation assay
After surface staining, the cells were incubated in PBS containing 40 μM of dichlorofluorescein diacetate (DCFDA; Life Technologies) for 30 min at 37 °C, to measure intracellular ROS.
Cell migration assay
The differences in migration of cells that had a mesenchymal cell origin was evaluated using the Oris™ Cell Migration Assay (Platypus Technologies, Madison, WI) according to the manufacturer’s protocol. In brief, isolated PVECs and mesenchymal cells from mouse lungs were stimulated with 20 μM LPS, and the cells were grown to 90% confluence before removal by trypsinization, resuspension in appropriate medium, and seeding into Oris™ Pro Collagen 96-well plates with an Oris™ cell seeding stopper to restrict cell seeding to the outer regions of the wells. The plates were seeded with 300,000 cells in 100 μl of appropriate medium per well. The seeded plates were incubated for 24 h at 37 °C in 5% CO2 to allow cell attachment, and the stoppers were then removed to create a 2 mm diameter detection zone into which cells could migrate. After removal of the stoppers, the 96-well plates were incubated for 48 h at 37 °C in 5% CO2 to allow time for migration, and the number of cells that had migrated into the detection zone was determined.
Values are shown as mean ± SEM unless otherwise described or the median (25–75th percentile). The results were analyzed using the Mann-Whitney test for comparison between any two groups, and by nonparametric equivalents of ANOVA for multiple comparisons. GraphPad PRISM software (Version 7.03; GraphPad Software, San Diego) was used for data analysis. The level of statistical significance was set at P < 0.05.
Vildagliptin attenuated pulmonary fibrosis induced by LPS
We used a post-ALI pulmonary fibrosis model in which LPS treatment of male C57BL/6 mice induced pulmonary fibrosis as described in a previous report .
Both flow cytometry (FCM) and immunohistochemical analysis revealed that CD26 expression in PVECs defined as CD31+CD45− cells was increased 14 days after LPS administration (Fig. 1a-c). Furthermore, Masson’s trichrome staining of lung sections to evaluate fibrotic lesions showed that recurrent LPS exposure led to prominent pulmonary fibrosis, and this fibrosis was attenuated in the presence of the DPP-4 inhibitor vildagliptin. (Fig. 1d, e).
Vildagliptin attenuated EndMT in PVECs
Hashimoto et al. reported that EndMT is involved in bleomycin-induced pulmonary fibrosis . However, less is known about the origin of pulmonary fibrosis in systemic endotoxin-induced ALI. In the pulmonary fibrosis model after systemic endotoxemia in which pathogenesis is initiated by endothelial injury, we surmised that EndMT is closely related to fibrotic processes.
We first evaluated whether EndMT is induced in a recurrent LPS ip model. FCM analyses indicated that representative mesenchymal markers, including α-SMA and S100A4, were highly co-expressed with the representative endothelial marker CD31 (Fig. 2a-d).
We next isolated PVECs using flow cytometry and evaluated gene expression by quantitative RT-PCR analyses. Gene expression of mesenchymal-specific markers (Col1a1, Col1a2 and S100a4) in isolated PVECs was significantly increased in LPS-treated mice compared to in vehicle-treated mice, whereas gene expression of endothelial-specific markers (Pecam1 and Cdh5) in isolated PVECs was significantly decreased in LPS-treated mice (Fig. 2e). Moreover, the gene expression of Twist 2, one of the transcription factors related to EndMT, was significantly increased in LPS-treated mice compared to in vehicle-treated mice. Interestingly, all of these changes in expression were significantly attenuated by systemic administration of vildagliptin (Fig. 2a-e). These results were consistent with those obtained in immunofluorescence analyses using triple staining for mesenchymal cell markers (α-SMA and S100A4), CD45 and CD31 (Fig. 3a, b).
Vildagliptin attenuated ROS production in PVECs in vivo
Since we recently reported that ROS is one of the key inducer of EndMT in septic lung injury , we next evaluated if vildagliptin attenuated ROS production in PVECs. As expected, intracellular ROS measured in PVECs using DCFDA significantly decreased in LPS-PVECs treated with vildagliptin (Fig. 5a).
Vildagliptin inhibited LPS-induced EndMT of HMVEC-Ls in the absence of immune cells or GLP-1
As we recently reported, LPS directly induces pulmonary vascular EndMT in the absence of immune cells in vitro . To evaluate the direct efficacy of vildagliptin in inhibiting LPS-induced EndMT in HMVEC-Ls, we next conducted in vitro experiments to test whether vildagliptin inhibited EndMT in the absence of immune cells or GLP-1.
While LPS exposure induced morphological change to a spindle-shaped phenotype, vildagliptin treatment attenuated the degree (Fig. 4a). In addition, FCM analyses revealed that vildagliptin treatment decreased upregulation of α-SMA and S100A4 expression in HMVEC-Ls (Fig. 4b). Immunocytochemistry also showed an increase in the number of α-SMA+-HMVEC-Ls 144 h after LPS challenge, whereas vildagliptin suppressed this increase. Since GLP-1 is produced and secreted by intestinal enteroendocrine epithelial cells, our experiments performed in vitro using a single vascular cell type provided results independent of GLP-1 participation. These data demonstrated that vildagliptin can attenuate the mesenchymal transition of endotoxin-treated PVECs partly independent of GLP-1 (Fig. 4c).
Vildagliptin attenuated ROS production in PVECs in vitro
Next, we evaluated if vildagliptin attenuated ROS production in HMVEC-Ls independent of GLP-1. Interestingly, expression of ROS was significantly decreased in LPS-HMVEC-Ls treated with vildagliptin in the absence of GLP-1 (Fig. 5b).
Linagliptin also inhibited LPS-induced EndMT of HMVEC-Ls in the absence of immune cells
To confirm different gliptin displays the same effects to HMVEC-Ls, we used linagliptin, which had been reported to ameliorate kidney fibrosis . Interestingly, linagliptin also inhibited EndMT of LPS-exposed HMVEC-Ls (Fig. 4a-c). Linagliptin also attenuated ROS production in HMVEC-Ls (Fig. 5b).
Taken together, DPP-4 inhibitors could directly inhibit EndMT partly with antioxidant pathway independent of GLP-1.
EndMT cells had higher proliferative activity than non-endothelium-derived mesenchymal cells
Finally, to evaluate the impact of attenuated EndMT, we analyzed the cytologic characteristics of EndMT cells in PVECs (CD31+/CD45−/CD326− cells) and pulmonary mesenchymal cells (CD31−/CD45−/CD326− cells) isolated from wild type mice using a BD FACS Aria II cell sorter. We then treated these two cell types with LPS for 96 h.
Similar to our previous report , almost all PVECs underwent a morphological change to acquire a spindle-like shape, and we defined these cells as EndMT-PVECs. A comparison of EndMT-PVECs and non-endothelium-derived mesenchymal cells (NEMCs) (CD31−/CD45−/CD326− cells treated with LPS for 96 h) in a cell migration assay showed that EndMT-cells had higher migration activity compared to non-endothelium-derived mesenchymal cells (Fig. 6a, b). Quantitative PCR analyses of expression of the proliferation marker Ki67 by EndMT-cells and NEMCs treated with LPS for 96 h showed significant upregulation of Ki67 mRNA levels in EndMT-cells (*P < 0.05, N = 5) (Fig. 6c).
In this study, we first demonstrated that pulmonary vascular EndMT occurred in a murine model of pulmonary fibrosis after systemic endotoxemic injury. Although we recently reported that single LPS administration to mice was associated with transient pulmonary vascular EndMT without pulmonary fibrosis, whether intermittent LPS stimulation could also promote pulmonary fibrosis via EndMT was unclear . Moreover, we also found that DPP-4 expression was increased in PVECs from a post-ALI pulmonary fibrosis murine model. Here we showed that treatment with the DPP-4 inhibitor vildagliptin effectively suppressed EndMT and had an anti-fibrotic effect in post-ALI pulmonary fibrosis.
Sepsis is the leading cause of ALI, which is characterized by endothelial activation and damage [25,26,27]. Although fibroblasts were long believed to originate directly from embryonic mesenchymal cells [28,29,30], endothelial cells are now seen as a source for fibroblasts in many tissues [7, 28, 31, 32]. The results of the present study demonstrate that persistent systemic endotoxemic injury also leads to pulmonary fibrosis via EndMT. Interestingly, interactions between LPS to PVECs could be in part direct and do not require immune cell mediation. These results are consistent with the clinical findings that acute lung injury develops in the presence of severe neutropenia.
Considering these results together with those shown in our recent report , pulmonary vascular EndMT is reversible and does not contribute to pulmonary fibrosis when endotoxemia is transient, but could lead to pulmonary fibrosis when endotoxemia persists. Although we have not determined whether pulmonary vascular EndMT is reversible in the post-ALI pulmonary fibrosis murine model, we did find that pulmonary fibrosis scores failed to improve 42 days after the initial administration of LPS (data not shown).
On the other hand, endotoxemia induces upregulation of DPP-4 expression in vascular endothelial cells, and DPP-4 inhibitors are reported to act as vascular endothelial protectors [19, 33, 34]. Examination of the role of DPP-4 in pulmonary disease was previously limited to respiratory epithelial injury such as bronchial asthma . Although DPP-4 was recently reported to be involved in pathologic features of asthmatic airway inflammation, cell proliferation, and fibronectin production , there are few studies concerning the role of DPP-4 in pulmonary vascular function. Thus, we hypothesized that the DPP-4 inhibitor vildagliptin could attenuate pulmonary fibrosis by inhibiting EndMT.
Our in vivo and in vitro results show that in our model of pulmonary fibrosis after systemic endotoxemic injury, DPP-4 expression is upregulated in PVECs in both the presence and absence of immune cells. Vildagliptin treatment attenuated the accumulation of DPP-4 in PVECs, and was associated with an inhibition of fibrotic change and reduced EndMT-cells in lungs. Although other means of DPP-4 inhibition that do not involve endothelial cells could have promoted the observed anti-fibrotic effects, we strongly believe in the clinical significance of endothelial DPP-4 in fibrotic disorders such as pulmonary fibrosis after systemic endotoxemic injury, in which vascular damage and activation of endothelial cells play a significant role. Indeed, our study showed that EndMT cells had higher proliferation and migration rates compared to non-endothelium-derived mesenchymal cells. These results might suggest the clinical significance of suppressing the activity of EndMT-cells in post-ALI pulmonary fibrosis via a DPP-4 pathway.
Another novelty of this study is to show a direct action of DPP-4 inhibitors on ROS production in PVECs and attenuating EndMT. Since Yan et al. demonstrated that GLP-1 treatment could protect against the hyperglycemia-induced EndMT , we expected in this study that the EndMT-inhibiting effect was mediated by GLP-1. Although that would be true, our cellular model confirmed that DPP-4 inhibitors could attenuate EndMT even in the absence of GLP-1. For investigating the mechanistic insight, we evaluated if DPP-4 inhibitors attenuate ROS production in PVECs, which was reported to be the key trigger of EndMT in LPS-induced lung injury . Interestingly, DPP-4 inhibitors directly induced antioxidant-response in PVECs. Taken together with our recent report, vildagliptin has been proven to protect against EndMT partly via suppressing ROS in PVECs, and it is partly independent of GLP-1.
Although oral DPP-4 inhibitors are used to treat diabetes , intraperitoneal injection of vildagliptin did not lead to significant hypoglycemia in this study (data not shown). This is consistent with earlier findings that DPP-4 inhibitors do not increase hypoglycemia rates, even though they increase insulin secretion in a glucose-dependent manner . In the presence of sepsis or septic lung injury, we encounter many patients who suffer from hyperglycemia due to increased insulin resistance . The target range for blood glucose in these conditions is the subject of considerable debate, but the lower end of the blood glucose range is not recommended for critically ill adults . There is also a significant relationship between acute glucose swings and activation of oxidative stress , which might lead to an increase in vascular endothelial cell injury and organ dysfunction. Vildagliptin has shown the ability to prevent pulmonary fibrosis and did not induce severe hypoglycemia in this study indicating it may be effective for systemic endotoxemic lung injury.
There are several limitations of this study that should be considered. First, we have not examined whether other DPP-4 inhibitors could be beneficial for inhibiting post-ALI pulmonary fibrosis in vivo. We chose vildagliptin for in vivo experiments since it is the only DPP-4 inhibitor which has previously been administered intraperitoneally to the best of our knowledge . An intermittent LPS-injected model revealed prominent oral intake loss for the first ten days, and their oral intake amount was unstable. Therefore, drugs which require oral administration are less reliable for these experiments, driving our decision to use vildagliptin. Shi et al. did report different activities in endothelial cells among various DPP-4 inhibitors , indicating that additional studies should focus on other DPP-4 inhibitors to determine whether these molecules have unique drug-specific effects. Second, we have only established the efficacy of vildagliptin in a preventive protocol, but not in a therapeutic protocol. To determine whether this molecular approach may have therapeutic relevance, we will need to start delivering vildagliptin from 4 or 5 days after initial LPS administration.
The current study demonstrated that in a pulmonary fibrosis murine model after systemic endotoxemic injury, EndMT was observed in endothelial cells that overexpressed DPP-4. Vildagliptin might play a beneficial role in ameliorating pulmonary fibrosis by inhibiting EndMT even in the absence of GLP-1.
Acute lung injury
Acute respiratory distress syndrome
Endothelial cell basal medium-2
Endothelial cell growth medium 2
Elastica van Gieson
Non-endothelium-derived mesenchymal cells
Pulmonary vascular endothelial cells
Reactive oxygen species
Transforming growth factor β
Ware LB, Matthay MA. The acute respiratory distress syndrome. N Engl J Med. 2000;342:1334–49.
Zhou WQ, Wang P, Shao QP, Wang J. Lipopolysaccharide promotes pulmonary fibrosis in acute respiratory distress syndrome (ARDS) via lincRNA-p21 induced inhibition of Thy-1 expression. Mol Cell Biochem. 2016;419:19–28.
Suzuki T, Tada Y, Nishimura R, Kawasaki T, Sekine A, Urushibara T, Kato F, Kinoshita T, Ikari J, West J, Tatsumi K. Endothelial-to-mesenchymal transition in lipopolysaccharide-induced acute lung injury drives a progenitor cell-like phenotype. Am J Physiol Lung Cell Mol Physiol. 2016;310:L1185–98.
Stenmark KR, Frid M, Perros F. Endothelial-to-Mesenchymal transition: an evolving paradigm and a promising therapeutic target in PAH. Circulation. 2016;133:1734–7.
Pardali E, Goumans MJ, ten Dijke P. Signaling by members of the TGF-beta family in vascular morphogenesis and disease. Trends Cell Biol. 2010;20:556–67.
Echeverria C, Montorfano I, Sarmiento D, Becerra A, Nunez-Villena F, Figueroa XF, Cabello-Verrugio C, Elorza AA, Riedel C, Simon F. Lipopolysaccharide induces a fibrotic-like phenotype in endothelial cells. J Cell Mol Med. 2013;17:800–14.
Hashimoto N, Phan SH, Imaizumi K, Matsuo M, Nakashima H, Kawabe T, Shimokata K, Hasegawa Y. Endothelial-mesenchymal transition in bleomycin-induced pulmonary fibrosis. Am J Respir Cell Mol Biol. 2010;43:161–72.
Ranchoux B, Antigny F, Rucker-Martin C, Hautefort A, Pechoux C, Bogaard HJ, Dorfmuller P, Remy S, Lecerf F, Plante S, et al. Endothelial-to-mesenchymal transition in pulmonary hypertension. Circulation. 2015;131:1006–18.
Choi SH, Hong ZY, Nam JK, Lee HJ, Jang J, Yoo RJ, Lee YJ, Lee CY, Kim KH, Park S, et al. A hypoxia-induced vascular endothelial-to-Mesenchymal transition in development of radiation-induced pulmonary fibrosis. Clin Cancer Res. 2015;21:3716–26.
Nickols J, Obiako B, Ramila KC, Putinta K, Schilling S, Sayner SL. Lipopolysaccharide-induced pulmonary endothelial barrier disruption and lung edema: critical role for bicarbonate stimulation of AC10. Am J Physiol Lung Cell Mol Physiol. 2015;309:L1430–7.
Nieto-Fontarigo JJ, Gonzalez-Barcala FJ, San Jose E, Arias P, Nogueira M, Salgado FJ. CD26 and asthma: a comprehensive review. Clin Rev Allergy Immunol. 2016;
Mamza J, Marlin C, Wang C, Chokkalingam K, Idris I. DPP-4 inhibitor therapy and bone fractures in people with type 2 diabetes - a systematic review and meta-analysis. Diabetes Res Clin Pract. 2016;116:288–98.
Nagamine A, Hasegawa H, Hashimoto N, Yamada-Inagawa T, Hirose M, Kobara Y, Tadokoro H, Kobayashi Y, Takano H. The effects of DPP-4 inhibitor on hypoxia-induced apoptosis in human umbilical vein endothelial cells. J Pharmacol Sci. 2017;133:42–8.
Salim HM, Fukuda D, Higashikuni Y, Tanaka K, Hirata Y, Yagi S, Soeki T, Shimabukuro M, Sata M. Dipeptidyl peptidase-4 inhibitor, linagliptin, ameliorates endothelial dysfunction and atherogenesis in normoglycemic apolipoprotein-E deficient mice. Vasc Pharmacol. 2016;79:16–23.
Manrique C, Habibi J, Aroor AR, Sowers JR, Jia G, Hayden MR, Garro M, Martinez-Lemus LA, Ramirez-Perez FI, Klein T, et al. Dipeptidyl peptidase-4 inhibition with linagliptin prevents western diet-induced vascular abnormalities in female mice. Cardiovasc Diabetol. 2016;15:94.
Oyama J, Higashi Y, Node K. Do incretins improve endothelial function? Cardiovasc Diabetol. 2014;13:21.
Remm F, Franz WM, Brenner C. Gliptins and their target dipeptidyl peptidase 4: implications for the treatment of vascular disease. Eur Heart J Cardiovasc Pharmacother. 2016;2:185–93.
Kohashi K, Hiromura M, Mori Y, Terasaki M, Watanabe T, Kushima H, Shinmura K, Tomoyasu M, Nagashima M, Hirano T. A Dipeptidyl Peptidase-4 inhibitor but not Incretins suppresses abdominal aortic aneurysms in Angiotensin II-infused Apolipoprotein E-null mice. J Atheroscler Thromb. 2016;23:441–54.
Steven S, Jurk K, Kopp M, Kroller-Schon S, Mikhed Y, Schwierczek K, Roohani S, Kashani F, Oelze M, Klein T, et al. Glucagon-like peptide-1 receptor signalling reduces microvascular thrombosis, nitro-oxidative stress and platelet activation in endotoxaemic mice. Br J Pharmacol. 2017;174:1620–32.
Gangadharan Komala M, Gross S, Zaky A, Pollock C, Panchapakesan U. Saxagliptin reduces renal tubulointerstitial inflammation, hypertrophy and fibrosis in diabetes. Nephrology (Carlton). 2016;21:423–31.
He Z, Zhu Y, Jiang H. Inhibiting toll-like receptor 4 signaling ameliorates pulmonary fibrosis during acute lung injury induced by lipopolysaccharide: an experimental study. Respir Res. 2009;10:126.
Ashcroft T, Simpson JM, Timbrell V. Simple method of estimating severity of pulmonary fibrosis on a numerical scale. J Clin Pathol. 1988;41:467–70.
Sekine A, Nishiwaki T, Nishimura R, Kawasaki T, Urushibara T, Suda R, Suzuki T, Takayanagi S, Terada J, Sakao S, et al. Prominin-1/CD133 expression as potential tissue-resident vascular endothelial progenitor cells in the pulmonary circulation. Am J Physiol Lung Cell Mol Physiol. 2016;310:L1130–42.
Kanasaki K, Shi S, Kanasaki M, He J, Nagai T, Nakamura Y, Ishigaki Y, Kitada M, Srivastava SP, Koya D. Linagliptin-mediated DPP-4 inhibition ameliorates kidney fibrosis in streptozotocin-induced diabetic mice by inhibiting endothelial-to-mesenchymal transition in a therapeutic regimen. Diabetes. 2014;63:2120–31.
Orfanos SE, Mavrommati I, Korovesi I, Roussos C. Pulmonary endothelium in acute lung injury: from basic science to the critically ill. Intensive Care Med. 2004;30:1702–14.
Peek GJ, Elbourne D, Mugford M, Tiruvoipati R, Wilson A, Allen E, Clemens F, Firmin R, Hardy P, Hibbert C, et al. Randomised controlled trial and parallel economic evaluation of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR). Health Technol Assess. 2010;14:1–46.
Wort SJ, Evans TW. The role of the endothelium in modulating vascular control in sepsis and related conditions. Br Med Bull. 1999;55:30–48.
Zeisberg EM, Tarnavski O, Zeisberg M, Dorfman AL, McMullen JR, Gustafsson E, Chandraker A, Yuan X, Pu WT, Roberts AB, et al. Endothelial-to-mesenchymal transition contributes to cardiac fibrosis. Nat Med. 2007;13:952–61.
Maric C, Ryan GB, Alcorn D. Embryonic and postnatal development of the rat renal interstitium. Anat Embryol (Berl). 1997;195:503–14.
Lang H, Fekete DM. Lineage analysis in the chicken inner ear shows differences in clonal dispersion for epithelial, neuronal, and mesenchymal cells. Dev Biol. 2001;234:120–37.
Sohal SS. Endothelial to mesenchymal transition (EndMT): an active process in chronic obstructive pulmonary disease (COPD)? Respir Res. 2016;17:20.
Abu El-Asrar AM, De Hertogh G, van den Eynde K, Alam K, Van Raemdonck K, Opdenakker G, Van Damme J, Geboes K, Struyf S. Myofibroblasts in proliferative diabetic retinopathy can originate from infiltrating fibrocytes and through endothelial-to-mesenchymal transition (EndoMT). Exp Eye Res. 2015;132:179–89.
Romacho T, Vallejo S, Villalobos LA, Wronkowitz N, Indrakusuma I, Sell H, Eckel J, Sanchez-Ferrer CF, Peiro C. Soluble dipeptidyl peptidase-4 induces microvascular endothelial dysfunction through proteinase-activated receptor-2 and thromboxane A2 release. J Hypertens. 2016;34:869–76.
Brenner C, Franz WM. Pharmacological DPP4 inhibition for the prevention of vascular diseases. Int J Cardiol. 2016;202:49.
Shiobara T, Chibana K, Watanabe T, Arai R, Horigane Y, Nakamura Y, Hayashi Y, Shimizu Y, Takemasa A, Ishii Y. Dipeptidyl peptidase-4 is highly expressed in bronchial epithelial cells of untreated asthma and it increases cell proliferation along with fibronectin production in airway constitutive cells. Respir Res. 2016;17:28.
Yan F, Zhang GH, Feng M, Zhang W, Zhang JN, Dong WQ, Zhang C, Zhang Y, Chen L, Zhang MX. Glucagon-like peptide 1 protects against hyperglycemic-induced endothelial-to-Mesenchymal transition and improves myocardial dysfunction by suppressing poly(ADP-ribose) polymerase 1 activity. Mol Med. 2015;21:15–25.
Amori RE, Lau J, Pittas AG. Efficacy and safety of incretin therapy in type 2 diabetes: systematic review and meta-analysis. JAMA. 2007;298:194–206.
Nauck MA, Vilsboll T, Gallwitz B, Garber A, Madsbad S. Incretin-based therapies: viewpoints on the way to consensus. Diabetes Care. 2009;32(Suppl 2):S223–31.
Bader MS. Hyperglycemia and mortality in elderly patients with Staphylococcus Aureus bacteremia. South Med J. 2007;100:252–6.
Finfer S, Chittock DR, Su SY, Blair D, Foster D, Dhingra V, Bellomo R, Cook D, Dodek P, Henderson WR, et al. Intensive versus conventional glucose control in critically ill patients. N Engl J Med. 2009;360:1283–97.
Monnier L, Mas E, Ginet C, Michel F, Villon L, Cristol JP, Colette C. Activation of oxidative stress by acute glucose fluctuations compared with sustained chronic hyperglycemia in patients with type 2 diabetes. JAMA. 2006;295:1681–7.
Smith EP, An Z, Wagner C, Lewis AG, Cohen EB, Li B, Mahbod P, Sandoval D, Perez-Tilve D, Tamarina N, et al. The role of beta cell glucagon-like peptide-1 signaling in glucose regulation and response to diabetes drugs. Cell Metab. 2014;19:1050–7.
Shi S, Kanasaki K, Koya D. Linagliptin but not Sitagliptin inhibited transforming growth factor-beta2-induced endothelial DPP-4 activity and the endothelial-mesenchymal transition. Biochem Biophys Res Commun. 2016;471:184–90.
We are grateful to Ikuko Sakamoto, Tomoko Misawa and Akiko Moriya for technical assistance for the experiments.
This study was supported by a Grant-in-Aid for Scientific Research (JSPS KAKENHI Grant Number G16 K19445) from the Japanese Ministry of Education and Science, and by the Uehara Memorial Foundation (to TS).
Availability of data and materials
All data generated and analyzed during the study are included in the published article and can be shared upon request.
Ethics approval and consent to participate
The animal experiment protocol was reviewed and approved by the Chiba University Institutional Animal Care and Use Committee.
Consent for publication
TS received research grant from GlaxoSmithKline. RN is a member of a department endowed by Actelion Pharmaceuticals.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Vildagliptin ameliorates pulmonary fibrosis in lipopolysaccharide-induced lung injury by inhibiting endothelial-to-mesenchymal transition (PDF 449 kb)