Human mesenchymal stromal cells broadly modulate high glucose-induced inflammatory responses of renal proximal tubular cell monolayers
Renal proximal tubular epithelial cells (RPTEC) are dysfunctional in diabetic kidney disease (DKD). Mesenchymal stromal cells (MSC) may modulate DKD pathogenesis through anti-inflammatory mediators. This study aimed to investigate the pro-inflammatory effect of extended exposure to high glucose (HG) concentration on stable RPTEC monolayers and the influence of MSC on this response.
Morphologically stable human RPTEC/TERT1 cell monolayers were exposed to 5 mM and 30 mM (HG) D-glucose or to 5 mM D-glucose + 25 mM D-mannitol (MAN) for 5 days with sequential immunoassays of supernatants and end-point transcriptomic analysis by RNA sequencing. Under the same conditions, MSC-conditioned media (MSC-CM) or MSC-containing transwells were added for days 4–5. Effects of CM from HG- and MAN-exposed RPTEC/MSC co-cultures on cytokine secretion by monocyte-derived macrophages were determined.
After 72–80 h, HG resulted in increased RPTEC/TERT1 release of interleukin (IL)-6, IL-8, monocyte chemoattractant protein (MCP)-1 and neutrophil gelatinase-associated lipocalin (NGAL). The HG pro-inflammatory effect was attenuated by concentrated (10×) MSC-CM and, to a greater extent, by MSC transwell co-culture. Bioinformatics analysis of RNA sequencing data confirmed a predominant effect of HG on inflammation-related mediators and biological processes/KEGG pathways in RPTEC/TERT1 stable monolayers as well as the non-contact-dependent anti-inflammatory effect of MSC. Finally, CM from HG-exposed RPTEC/MSC transwell co-cultures was associated with attenuated secretion of inflammatory mediators by macrophages compared to CM from HG-stimulated RPTEC alone.
Stable RPTEC monolayers demonstrate delayed pro-inflammatory response to HG that is attenuated by close proximity to human MSC. In DKD, this MSC effect has potential to modulate hyperglycemia-associated RPTEC/macrophage cross-talk.
Advanced glycation end-products
Bone marrow-derived mesenchymal stromal cells
Differentially expressed gene
Diabetic kidney disease
Dulbecco’s modified Eagle medium
End-stage renal disease
Foetal calf serum
Granulocyte macrophage colony stimulating factor
Human corneal endothelial cell
Human serum albumin
Human telomerase reverse transcriptase
Monocyte chemoattractant protein 1
Mesenchymal stromal cell
Neutrophil gelatinase-associated lipocalin
RNA integrity number
Reactive oxygen species
Renal proximal tubular epithelial cell
Tumour necrosis factor alpha
Diabetic kidney disease (DKD) is the leading cause of end stage renal disease (ESRD) worldwide . The complex pro-inflammatory milieu of hyperglycaemia, reactive oxygen species (ROS), advanced glycation end products (AGE) and angiotensin-II contributes to activation of transcription factors, growth factors, inflammatory cytokines and chemokines that mediate glomerular, microvascular and tubulo-interstitial injury—eventually leading to progression to ESRD and to the increased cardiovascular mortality associated with DKD [2, 3, 4].
A substantial body of research evidence documents the links between chronic inflammation and the development and progression of DKD [5, 6, 7, 8]. Hyperglycaemia induces cytokine production by macrophages and other immune cells which may serve both as drivers and predictive biomarkers for progressive loss of renal function [7, 9, 10]. For example, circulating concentration of monocyte chemoattractant protein-1 (MCP-1/CCL2) has been shown to correlate with the degree of interstitial macrophage infiltration in human DKD while, experimentally, inhibition of MCP-1 in models of diabetes mellitus (DM) ameliorates renal injury [11, 12, 13]. Hyperglycaemia upregulates MCP-1 production by kidney tubular epithelial cells, leading to infiltration of monocytes into the kidneys where they may subsequently become differentiated into inflammatory macrophages [14, 15]. This is further associated with localised release of pro-inflammatory cytokines such as interleukin (IL)-1β, IL-6 and tumour necrosis factor-alpha (TNFα) [15, 16].
The renal proximal tubular epithelial cell (RPTEC) is a significant target for the adverse effects of chronic hyperglycaemia. Excessive glucose in the glomerular filtrate drives increased glucose reabsorption in the proximal tubules and activates a range of maladaptive pathways within RPTEC that contribute to the DKD pathogenesis [17, 18, 19, 20, 21, 22]. As DKD progresses, secondary mediators including growth factors, angiotensin-II and AGE activate inflammatory signalling pathways to further increase ROS production, inflammation, tubular cell hypertrophy and interstitial fibrosis [17, 18, 19, 21]. These insights highlight RPTEC as a potentially important therapeutic target in DKD, and in vitro studies involving cultured RPTEC-like cells provide a valuable test-bed for identifying and evaluating novel interventional strategies [21, 23]. Among the in vitro tools available, RPTEC/TERT1 is an immortalised RPTEC cell line generated by overexpression of human telomerase reverse transcriptase (hTERT) . Recent studies have highlighted the potential advantages of RPTEC/TERT1 stable monolayer cultures over other cell lines for modelling renal proximal tubular function and responses [25, 26, 27].
Macrophages are key mediators of intra-renal inflammation in DM, being an important source of pro-inflammatory factors including IL-1, TNFα, IL-6 and ROS . In vivo, macrophage infiltration and activation within the kidneys of diabetic animals as well as other models of renal injury has been shown to contribute significantly to increased production of chemokines, interstitial fibrosis and increased serum creatinine and proteinuria [29, 30, 31, 32]. Combined with the direct effects of chronic hyperglycaemia to induce pro-inflammatory responses in RPTEC, these studies indicate that crosstalk between RPTEC and interstitial macrophages within the kidney represents a key pathological axis in the development and progression of DKD.
Currently, a limited number of therapies are available that specifically target the development and progression of DKD. Novel interventions that modulate multiple inflammatory pathways as well as promote repair of tubule-interstitial injury could well complement conventional drug classes that predominantly address maladaptive glomerular pathophysiology in DKD. Relevant to this, interventions to inhibit pro-inflammatory cross-talk between RPTEC and macrophages represent an attractive strategy. Mesenchymal stem/stromal cell (MSC) therapy is a potential therapeutic option for diverse inflammatory disease pathologies [2, 33, 34]. In their physiological, perivascular niches in the bone marrow and other tissues, MSC have critical roles in immunomodulation and self-renewal [2, 34, 35]. Recent studies in animal models of DKD indicate that systemic administration of MSC ameliorates DM-associated albuminuria and renal pathological abnormalities in a paracrine manner through immunomodulatory and anti-apoptotic effects [36, 37, 38, 39]. The potential clinical translation of MSC therapy for progressive DKD has reached the stage of early-phase clinical trials but the precise mechanisms of action of MSC remain incompletely characterised.
In this study, we aimed to determine the immunological consequences of prolonged exposure of RPTEC/TERT1 stable monolayers to high concentrations of glucose and to investigate the modulatory effects of culture-expanded human MSC and their soluble products on high glucose (HG)-induced RPTEC inflammatory response and the resulting RPTEC/macrophage cross-talk.
RPTEC/TERT1 cell culture and treatments
RPTEC/TERT1 (human renal proximal tubular epithelial cell line from the American Tissue Culture Collection) were cultured in 24-well flat-bottom plates (Sarstedt, Numbrecht, Germany) in Dulbecco’s modified Eagle’s medium (DMEM) (Gibco, Grand Island, NY, USA) and Ham’s F-12 medium (Gibco) at 1:1 supplemented with ITS (Sigma Aldrich, St. Louis, MO, USA) containing 10 μg/ml insulin, 5.5 μg/ml transferrin and 5 ng/ml sodium selenite; 10 ng/ml epidermal growth factor (Sigma); 36 ng/ml hydrocortisone (Sigma); 2 mM l-glutamine (Gibco) and 100 U/ml penicillin and 100 μg/ml streptomycin (Gibco) and maintained at 37 °C, 5% CO2 in a humidified tissue culture incubator. For stabilisation of the monolayer, 27,500 cells/cm2 were plated, cultured for 6 days to 100% confluency then allowed to form stable monolayers for a further 6 days before use in individual experiments. The medium was replaced every 2 days. For “high glucose (HG)” and “mannitol osmotic control (MAN)” culture conditions, the medium was additionally supplemented with 25 mM D-glucose (Sigma) or 25 mM D-mannitol (Sigma) respectively was added at day 12 and maintained for a further 4–5 days. In some experiments, the medium was also supplemented with 100 μg/ml human serum albumin (Sigma), or 1 ng/ml IL-1β (Peprotech EC Ltd., NJ, USA) and 20 ng/ml TNFα (Peprotech) for the final 5 or 2 days of culture respectively. Phase-contrast microscopy and image capture of cultured cells were performed at intervals using an Olympus-IX71 inverted microscope (Tokyo, Japan). Osmolality of the cell culture supernatants from CTRL, HG and MAN conditions was measured in the Clinical Biochemistry Laboratory, Galway University Hospitals.
Culture of mesenchymal stromal cells and control cells
Cryopreserved human bone marrow-derived MSC (BM-MSC) from two healthy donors were cultured in MEM-Alpha media (Gibco) supplemented with 10% extracellular vesicle (EV)-free heat-inactivated foetal calf serum (FCS) (Gibco), 1% penicillin/streptomycin (Gibco) and 1 ng/ml fibroblast growth factor (R&D Systems, Minneapolis, MN, USA). EV-free FCS was prepared by ultracentrifugation of FCS at 100,000×g (Sorvall 100SE Ultra Centrifuge) for 18 h and subsequent collection of supernatants. Culture of human corneal endothelial cells (HCEC) was carried out in DMEM supplemented with 10% FCS (Gibco) and 1% penicillin/streptomycin (Gibco). Conditioned media were prepared as described in Additional file 1: Supplementary Methods. In the case of the MSC-derived CM, this was further divided into non-manipulated CM (“MSC-CM (Whole)”) and MSC-CM from which the MSC-derived EV were depleted by ultracentrifugation for 18 h as 100,000×g (“MSC-CM (-EV)”).
Indirect co-culture of RPTEC/TERT1 cells and mesenchymal stromal cells
RPTEC/TERT1 cells were plated at 27,500 cells/cm2 in six-well tissue culture plates and were cultured for 12 days to form stable monolayers. The cells were then cultured in medium additionally supplemented with 25 mM D-glucose (Sigma) or D-mannitol (Sigma) for a further 5 days as described above. Human BM-MSC were separately seeded at 10,000 cells/cm2 into transwell inserts (ThinCert™, Greiner Bio-One, Kremsmünster, Austria) for 3 days in MSC culture medium. On day 15 of RPTEC/TERT1 cell culture, the BM-MSC-containing inserts were placed on top of individual RPTEC/TERT1 monolayer-containing wells and these co-cultures were maintained for a further 2 days, following which the RPTEC/TERT1 cell pellets and supernatants were collected for protein analysis and enzyme-linked immunosorbent assays (ELISA) respectively. Transwell co-cultures of RPTEC/TERT1 cells and HCEC were carried out by the same protocol.
Enzyme-linked immunosorbent assays
Assay kits for Interleukin-1β (IL-1β), IL-6, IL-8, TNFα, IL-10, MCP-1 and neutrophil gelatinase-associated lipocalin (NGAL) (R&D Systems, MN, USA) were used to perform ELISAs of culture supernatants according to the manufacturer’s instructions (see Additional file 1: Supplementary Methods for a detailed protocol).
Viability of RPTEC/TERT1 cells was determined by propidium iodide (PI) (Molecular Probes, Oregon, USA) staining. In brief, following trypsinization and centrifugation, cell pellets were re-suspended in culture medium and incubated for 15 min at 37 °C to restore membrane integrity. The cell suspensions were then washed and re-suspended in FACS buffer containing 2% FCS (Gibco) and 0.05% NaN2 (Sigma) in PBS (Sigma). Cells were transferred as 100-μl aliquots into 5-ml polystyrene FACS tubes (Sarstedt). Finally, PI solution was added to final concentration of 1 μg/ml and the samples were analysed on an Accuri-C6 flow cytometer (Becton Dickinson, USA) using CFlow software.
Immunoblots of RPTEC-derived protein lysates for NF-κB p65, phospho-NF-kB p65 (pP65), p38 MAPK, phospho-p38 MAPK (pP38MAPK), p44/42 MAPK (Erk1/2), phospho-p44/42 MAPK (pErk1/2; Thr202/Tyr204), STAT1, phospho-Stat1 (pSTAT1; Tyr701), protein kinase-C alpha (PKCα), phospho-PKCα/β II (pPKCα; Thr638/641) and PPAR-γ were performed using reagents and procedures described in Additional file 1: Supplementary Methods.
RNA isolation and quantification
Total RNA was isolated from RPTEC/TERT1 cells using TRIzol/Chloroform method and by RNEasy Midi Kit (Qiagen, Hilden, Germany). A detailed protocol for RNA isolation by TRIzol method is provided in Additional file 1: Supplementary Methods. For samples prepared using RNEasy Midi Kit (Qiagen), the manufacturer’s recommended protocol was followed. The quality and integrity of all RNA samples were measured by Bioanalyzer-2100 using RNA 6000 Pico kit (Agilent Technologies) according to the manufacturer’s recommended protocol.
RNA sequencing and bioinformatics analysis
High-throughput RNA sequencing (RNA-seq) was performed by BGI Genomics Service (Hong Kong) using BGISEQ-500, and Bioinformatics analyses of the resulting transcriptional profiles were performed using a suite of software packages including RSEM (quantitation of gene expression level), Cluster and Java Treeview Cluster (clustering analysis of gene expressions), Medusa (protein-protein interactions), WCGNA and Cytoscape (gene co-expression network analysis). Only RNA samples with RNA integrity number (RIN) ≥ 7.0 were subjected to RNA-seq. In brief, following fragmentation of mRNA and subsequent reverse transcription and amplification, a sequencing library was prepared. Nucleotide sequence of the fragments was determined and high-quality reads were aligned to the reference genomic sequence. Fragments that matched the genomic sequence were assigned to a specific position of a specific chromosome in the genome; thereby, the gene fragments could be linked to a specific gene. The number of reads per gene were counted and normalised. The criteria for designation of differentially expressed genes (DEG) were > 1.5 absolute fold-change and statistical significance (p < 0.05) among experimental conditions. RNA-seq data analyses involved plotting data using principal component analysis and KEGG pathway enrichment analysis.
Quantitative, reverse transcription polymerase chain reaction (qRT-PCR)
For qRT-PCR, the Luna Universal Probe One Step RT-qPCR kit (New England BioLabs, MA, USA) was used according to the manufacturer’s instructions. Reactions consisted of 50 ng RNA samples, mastermix, nuclease-free water, enzyme and primer/probe in a final volume of 10 μl. Individual target specific primers (both forward and reverse; for IL-6, MCP-1, IL-1β, IL-8, TNFα, NGAL and RPLP0) and TaqMan probes (for quantitation) were purchased from Integrated DNA Technologies (Coralville, Iowa, USA). The primer sequences are listed in Additional file 2: Table S1. The reactions were performed on Step-One Plus PCR instrument (Applied Biosystems, Waltham, MA, USA). Mean Ct values were used to calculate the fold changes in the expression of different target genes (for IL-6, MCP-1, IL-1β, IL-8, TNFα and NGAL) in treatment groups vs. control as determined relative to the housekeeping gene RPLP0 using the 2–∆∆Ct method.
Culture of primary human macrophages and exposure to conditioned media
Human peripheral blood mononuclear cells (PBMCs) were prepared and cultured overnight using a standard protocol (described in detail in Additional file 1: Supplementary Methods). Plastic-adherent PBMCs were cultured in 24-well plates (Sarstedt) at a density of 22,500 cells/cm2 in macrophage medium containing 20 ng/ml granulocyte macrophage colony stimulating factor (GM-CSF, Peprotech). Medium was replaced every 3 days. After 9 days, the medium was replaced with conditioned medium (CM) from the RPTEC/TERT1 co-culture experiments with addition of GM-CSF to a final concentration of 20 ng/ml. To some wells, 100 ng/ml interferon gamma (IFNγ, Peprotech), 100 ng/ml TNFα (Peprotech) and 50 ng/ml LPS (Sigma) were added to provide a positive control for pro-inflammatory stimulation. After 24 h, the CM was removed, the macrophages were washed with PBS and fresh macrophage medium containing GM-CSF was added. Finally, after an additional 24 h of culture, the supernatants were collected for subsequent analysis by ELISA.
Statistical analysis was performed using GraphPad Prism version 6.0. Paired- or unpaired Student’s t test, non-parametric multiple t test and one- or two-way ANOVA were used for analysis of individual experiments as appropriate. Details of statistical analyses performed for specific experiments are provided in individual figure legends. For all statistical analyses, the threshold for significance was < 0.05. Experiments were performed at least three times unless otherwise stated in the figure legends.
Prolonged exposure to high glucose enhances inflammatory response of RPTEC/TERT1 monolayers
Conditioned medium from human mesenchymal stromal cells inhibits the high glucose-induced inflammatory response of RPTEC/TERT1 monolayers
Indirect co-culture of human mesenchymal stromal cells causes a more potent inhibition of high glucose-induced inflammatory response of RPTEC/TERT1
Prolonged exposure of RPTEC/TERT1 monolayers to high glucose concentration is associated with widespread transcriptional modifications that are modulated by indirect co-culture with MSC
Overall, it was concluded from the transcriptional profiling analyses of RPTEC/TERT1 monolayers that prolonged exposure to HG results in enhanced expression/activity of a wide range of genes and pathways associated with immune response and inflammation and that proximity to viable human BM-MSC for 48 h exert a broad inhibitory effect on many of these inflammatory pathways—likely through the production of soluble mediators. Furthermore, the anti-inflammatory effect of MSC on proximal tubular epithelial monolayers is not exclusive to a HG-induced pro-inflammatory response, as it was also evident under MAN (osmotic control) conditions.
Indirect mesenchymal stromal cell contact modulates pro-inflammatory cross-talk between high glucose-exposed RPTEC/TERT1 cell monolayers and human macrophages
A growing body of evidence indicates that RPTEC play an important role in the pathogenesis of DKD [17, 21, 25, 39, 40, 41]. In vitro observations using immortalised cell lines such as HK-2 provide a valuable, simplified system in which to explore specific effects of the diabetic milieu on renal epithelial cell biology but have limitations when comparing with primary RPTEC. Recent studies suggest that stable monolayers of RPTEC/TERT1 cells provide superior phenotypic and functional comparability to primary tubular epithelium [24, 25, 26, 27]. In our hands, in keeping with previous reports [24, 25, 26, 27], RPTEC/TERT1 cells formed stable monolayers after 12 days with an epithelial-like, cobblestone morphology which remained stable following a further 5-day exposure to HG or MAN. In this system, we observed that prolonged HG exposure induced a heightened inflammatory phenotype characterised by progressively increasing secretion of IL-6, IL-8 and MCP-1 along with greater release of the tubular injury biomarker NGAL. For IL-6 and MCP-1, our observations are comparable to those of Tang et al. in confluent, growth-arrested primary RPTEC, albeit only becoming evident compared to normal glucose and MAN controls following a longer exposure time . Importantly, although RNA-seq analysis revealed a range of other gene expression changes, we did not observe overt toxicity or evidence of loss of epithelial-like morphology of the monolayers during the period of exposure to HG or MAN.
Consistent with the HG-induced increase in IL-6 secretion by RPTEC/TERT1 monolayers, patients with DKD have increased renal IL-6 expression which correlates with kidney hypertrophy and albuminuria [43, 44] and increases with stage of DKD . Exposure to HG for 96 h or more also resulted in increased secretion of IL-8 by RPTEC/TERT1 cells. Of interest, Tashiro et al. reported increased levels of IL-8 in urine samples from the patients with early-stage DKD  while others observed increased IL-8 production by tubular epithelial cells via activation of NF-κB, ERK1/2 and STAT1 signalling in a glycated-albumin-induced diabetes model . Similarly, NF-κB-dependent upregulation of MCP-1 in albumin-treated RPTEC and increased MCP-1 expression in kidney biopsy samples from patients with DKD have been reported [48, 49]. In a hyperglycaemic environment, increased MCP-1 production by mesangial and tubular epithelial cells has also been observed in vitro [14, 50]. Functionally, tubular cell-derived MCP-1 triggers infiltration of the interstitium by monocytes which, along with resident macrophages, secrete additional pro-inflammatory cytokines . We also describe here a progressive increase in the release of NGAL, a comparatively new biomarker of DKD, following exposure of RPTEC/TERT1 stable monolayers to HG for 80 h or more. Of relevance, NGAL is elevated in serum and urine of DKD patients [51, 52, 53]. Furthermore, Nielsen et al. demonstrated an association between urinary NGAL and rate of eGFR decline with the implication that renal tubular cells represent the major source of the urinary NGAL release . Taken together, these observations support the relevance of our findings in the RPTEC/TERT1 culture system to renal interstitial inflammatory events related to hyperglycaemia and diabetes.
Human bone marrow-derived MSC produce immunomodulatory and cytoprotective mediators that act in a paracrine manner on a range of target cells to downregulate the production of pro-inflammatory cytokines and inhibit inflammatory signalling pathways [36, 54, 55, 56]. In animal models of diabetes, hBM-MSC infusions reduced matrix deposition in the mesangium  and glomerulus . Nagaishi et al. studied the effects of BM-MSC treatment in insulin-deficient and insulin-resistant DKD models and demonstrated the benefits following systemic administration of both cells and CM . Similarly, Lv et al. reported reduced intra-renal expression of IL1-β, IL-6, TNFα and MCP-1 following intravenous injection of MSC in a streptozotocin-induced rat model of DKD . The reduction in MCP-1 and other inflammatory cytokines was associated with decreased macrophage infiltration and reduced severity of renal structural injury. In keeping with these in vivo findings, our experiments to evaluate the effect of human BM-MSC on human RPTEC/TERT1 cells in the setting of prolonged HG exposure revealed anti-inflammatory effects both of MSC-CM and of indirect (transwell) co-culture of RPTEC-TERT1 cells with MSC—with the latter being more potent. To our knowledge, this is the first study to show the effect of MSC and their soluble products on RPTEC/TERT1 cells as an in vitro model of diabetic proximal tubulopathy. The results indicate that MSC have the potential to modulate RPTEC dysfunction in DKD either from a distant anatomical site or locally within the kidney. Perhaps surprisingly, MSC-CM depleted of EV had comparable anti-inflammatory effects to those of EV-containing CM, indicating that the paracrine anti-inflammatory effects were unlikely to be mediated by MSC-derived EV despite evidence that they may have reno-protective properties [57, 58]. Whether purified MSC-EV may have a distinct modulatory effect on HG-induced inflammatory responses of RPTEC/TERT1 monolayers and, if so, what mechanisms underlie such an effect remain an interesting question that merits further investigation.
Although knowledge of the mechanism of action of MSC in vivo is incomplete, the paracrine effect of a range of inducible factors is well established. Transcriptomic analysis of RPTEC/TERT1 cell monolayers demonstrated that prolonged HG exposure was associated with gene expression changes that were enriched for biological processes and signalling pathways of relevance to immune response and inflammation. We also observed differential gene expression between MAN and CTRL culture conditions that likely reflect the influence of increased osmolality on RPTEC-TERT1 monolayers. However, the findings that higher numbers of DEGs were identified for HG vs CTRL than for MAN vs CTRL and that the HG condition separated fully from CTRL and MAN on a principal component analysis of the RNA-seq data are in keeping with a distinct effect of HG rather than a non-specific effect of increased osmolality. Interestingly, under both HG and MAN conditions, the modulatory effects of indirect co-culture with MSC on the RPTEC-TERT1 monolayer transcriptome were also enriched for immune/inflammatory pathways—with the TNF signalling pathway being particularly prominent. Modulation of the HG-induced TNF signalling pathway following MSC co-culture included reversion toward control levels of the increased expression of genes related to leukocyte recruitment (CCL2/MCP-1, CXCL1, CXCL2, CXCL3), leukocyte activation (CSF-2), inflammatory cytokines (IL-1β, IL-6) and cell adhesion (E-Selectin). Results for several inflammatory mediators/products (IL-6, IL-8, CCL2/MCP-1 and LCN2/NGAL) were consistent across RNA-seq, qRT-PCR and ELISA. An overall implication of these results is that human MSC, delivered directly to the kidney or transmigrating to renal interstitial spaces in the setting of diabetes/hyperglycemia, are likely to initiate a paracrine interaction with RPTEC that potently downregulates chronic inflammatory signalling. Furthermore, we provide evidence that the modulatory effect of MSC on release of inflammatory mediators by RPTEC in the setting of HG may have downstream effects on the response of monocyte-derived macrophages which are known to infiltrate the kidney and mediate renal interstitial damage during DKD . Inflammatory stimuli to RPTEC have been shown to result in cross-talk with intra-renal macrophages through a number of mechanisms including cytokine/chemokine secretion, transfer of bioactive molecules in extracellular vesicles, release of danger-associated molecular patterns and triggering of specific forms of necrotic cell death [59, 60, 61].
A relatively large body of literature exists in support of the potential benefits of MSC to slow the progression of DKD through anti-inflammatory mechanisms . To date, however, only one early-phase clinical trial of a stromal cell therapy has been completed in human subjects with DKD. This demonstrated that, in relatively advanced DKD due to type 2 DM, intravenous injection of allogeneic bone marrow-derived Stro3+ mesenchymal precursor cells was safe up to 24 weeks post-administration and was associated with preliminary evidence of efficacy including decreased serum IL-6 compared to placebo .
In addition to the obvious caveat that experimental work conducted in vitro using a cell line will require validation in more physiologically relevant systems, some specific limitations of the study must be acknowledged. Firstly, while our culture conditions and experimental durations are quite comparable to those used by other investigators who have extensively characterised RPTEC/TERT1 cell epithelial monolayer formation , they cannot be said to be identical. Thus, the influence of variability in culture conditions on the physiological relevance of our experimental findings cannot be fully determined. Nonetheless, it is clear that, in our hands, the cells consistently generated typical, mature epithelial-like monolayers and that subsequent 4–5-day exposure of the monolayers to HG and MAN did not result in overt cellular toxicity or transformation to a non-epithelial phenotype. Lack of elucidation of a clear intracellular signalling mechanism to explain HG-induced changes in the expression and secretion of inflammatory mediators by RPTEC/TERT1 cell monolayers (and its suppression by factors released by MSC) is a second limitation. While involvement of alternative signalling pathways, of post-transcriptional/post-translation modification of the gene products or of altered intracellular trafficking/secretion of inflammatory mediators may explain the observations, it is also possible that experiments carried out at earlier or later time-points could have revealed increased activity of one or more predicted signalling pathways under HG conditions. Thirdly, while our experimental focus for the study was on HG-induced inflammatory response of RPTECT/TERT1 monolayers and its modulation by MSC, other potentially important aspects of the altered transcriptomic profiles revealed by RNA-seq have not been functionally validated and explored. By sharing the full lists of DEG we have identified under different experimental conditions, we anticipate that these data can be further exploited through deeper functional investigation by others in the field. Finally, a limitation of our experiments involving the transfer of conditioned media from RPTEC/MSC co-cultures to primary macrophages is that they do not exclude the possibility that MSC- and RPTEC/TERT1-derived soluble mediators act on macrophages independently of each other rather than as a result of a distinctive MSC/RPTEC cross-talk. Thus, additional experiments beyond the scope of the current study will be needed to dissect the individual mechanistic contributions of RPTEC and MSC on downstream activity of macrophages and to investigate the potency of MSC to regulate RPTEC signalling to macrophages across a range of pathogenic conditions.
Our current study reveals a predominantly pro-inflammatory effect of prolonged HG exposure on stable monolayers of the RPTEC/TERT1 cell line during a 5-day time window that is substantially modulated at a transcriptional level by soluble products of human MSC—particularly when the two cell types were cultured in close proximity. Experimentally, we also show that the combined secretome of RPTEC/MSC co-cultures has the capacity to dampen macrophage inflammatory response under HG conditions. These results provide a novel platform for better understanding anti-inflammatory mechanisms of action of MSC in in vivo studies and clinical trials of DKD. Our in vitro system also has the potential for identifying new targets of intervention for diabetes-associated proximal tubulopathy and pro-inflammatory epithelial cell/macrophage cross-talk. Further studies are also needed to elucidate the mechanisms whereby HG exposure induces a prolonged increased secretion of cytokines, chemokines and markers of inflammation by RPTEC in the absence of persistent over-activity of NF-κB, MAPK and other expected intracellular signalling pathways.
All flow cytometry experiments were performed in the NUI Galway Flow Cytometry Core Facility which is supported by funds from NUI Galway, Science Foundation Ireland, the Irish Government’s Programme for Research in Third Level Institutions, Cycle 5 and the European Regional Development Fund. The materials presented and views expressed here are the responsibility of the author(s) only. Human corneal endothelial cells were kindly provided by Prof. Thomas Ritter, REMEDI, School of Medicine, NUI Galway. We wish to acknowledge the generous assistance of Dr. Paula O’Shea, Clinical Biochemistry Laboratory, Galway University Hospitals for facilitating the analysis of culture supernatant osmolality.
MNI contributed to the conception and design, collection and/or assembly of data, data analysis and interpretation, manuscript writing, and final approval of the manuscript. TPG contributed to the conception and design, collection and/or assembly of data, data analysis and interpretation, and final approval of the manuscript. ES contributed to the collection and/or assembly of data, data analysis and interpretation, and final approval of the manuscript. SR contributed to the collection and/or assembly of data, data analysis and interpretation, and final approval of the manuscript. JQ contributed to the collection and/or assembly of data, data analysis and interpretation, and final approval of the manuscript. JC contributed to the collection and/or assembly of data and final approval of the manuscript. JMcC contributed to the provision of study material and final approval of the manuscript. TMcM contributed to the conception and design, provision of study material, data analysis and interpretation, and final approval of manuscript. MDG contributed to the conception and design, financial support, data analysis and interpretation, manuscript writing, and final approval of manuscript.
The research was supported by a grant from the European Commission [Horizon 2020 Collaborative Health Project NEPHSTROM (grant number 634086; TPG, MNI, MDG)]. Other funding sources that contributed to the work were grants from the European Commission [FP7 Collaborative Health Project VISICORT (grant number 602470; MDG, JC)], from Science Foundation Ireland [REMEDI Strategic Research Cluster (grant number 09/SRC-B1794; MDG) and CÚRAM Research Centre (grant number 13/RC/2073; MDG)], from the Health Research board of Ireland (grant number HRA_POR/2013/341; JC, MDG) and the European Regional Development Fund. TPG is supported by a Hardiman Scholarship from the College of Medicine, Nursing and Health Science, National University of Ireland Galway and a bursary from the Irish Endocrine Society/Royal College of Physicians of Ireland. JMcC and TMcM are funded by Science Foundation Ireland (grant number 12/IP/1686) and by the School of Biomolecular and Biomedical Science, University College Dublin.
The EU Commission takes no responsibility for any use made of the information set out.
Ethics approval and consent to participate
Human healthy volunteer bone marrow samples were sourced through the HRB Clinical Research Facility Galway according to a protocol approved by the Clinical Research Ethics Committee of the Galway University Hospitals. Primary culture expansion of MSC from bone marrow samples was performed at the Centre for Cell Manufacturing Ireland, National University of Ireland Galway.
Consent for publication
The authors declare that they have no competing interests.
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