Intra-pancreatic tissue-derived mesenchymal stromal cells: a promising therapeutic potential with anti-inflammatory and pro-angiogenic profiles
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Human pancreata contain many types of cells, such as endocrine islets, acinar, ductal, fat, and mesenchymal stromal cells (MSCs). MSCs are important and shown to have a promising therapeutic potential to treat various disease conditions.
We investigated intra-pancreatic tissue-derived (IPTD) MSCs isolated from tissue fractions that are routinely discarded during pancreatic islet isolation of human cadaveric donors. Furthermore, whether pro-angiogenic and anti-inflammatory properties of these cells could be enhanced was investigated.
IPTD-MSCs were expanded in GMP-compatible CMRL-1066 medium supplemented with 5% human platelet lysate (hPL). IPTD-MSCs were found to be highly pure, with > 95% positive for CD90, CD105, and CD73, and negative for CD45, CD34, CD14, and HLA-DR. Immunofluorescence staining of pancreas tissue demonstrated the presence of CD105+ cells in the vicinity of islets. IPTD-MSCs were capable of differentiation into adipocytes, chondrocytes, and osteoblasts in vitro, underscoring their multipotent features. When these cells were cultured in the presence of a low dose of TNF-α, gene expression of tumor necrosis factor alpha-stimulated gene-6 (TSG-6) was significantly increased, compared to control. In contrast, treating cells with dimethyloxallyl glycine (DMOG) (a prolyl 4-hydroxylase inhibitor) enhanced mRNA levels of nuclear factor erythroid 2-related factor 2 (NRF2) and vascular endothelial growth factor (VEGF). Interestingly, a combination of TNF-α and DMOG stimulated the optimal expression of all three genes in IPTD-MSCs. Conditioned medium of IPTD-MSCs treated with a combination of DMOG and TNF-α contained higher levels of pro-angiogenic (VEGF, IL-6, and IL-8) compared to controls, promoting angiogenesis of human endothelial cells in vitro. In contrast, levels of MCP-1, a pro-inflammatory cytokine, were reduced in the conditioned medium of IPTD-MSCs treated with a combination of DMOG and TNF-α.
The results demonstrate that IPTD-MSCs reside within the pancreas and can be separated as part of a standard islet-isolation protocol. These IPTD-MSCs can be expanded and potentiated ex vivo to enhance their anti-inflammatory and pro-angiogenic profiles. The fact that IPTD-MSCs are generated in a GMP-compatible procedure implicates a direct clinical application.
KeywordsMesenchymal stromal cells Anti-inflammatory Angiogenesis Type 1 diabetes TSG-6 NRF2 VEGF
Human platelet lysate
Human umbilical vein endothelial cells
Monocyte chemoattractant protein-1
Matrix metallopeptidase 2
Matrix metallopeptidase 9
Mesenchymal stromal cell
Nuclear factor erythroid 2–related factor 2
Type 1 diabetes
Tumor necrosis factor alpha-stimulated gene-6
Vascular endothelial growth factor
Mesenchymal stromal cells (MSCs) have the potential for treating various diseases . Currently, over 800 clinical trials involving MSCs have been registered (clinicaltrials.gov), the majority of which are focusing on the application of MSCs to diseases of the musculoskeletal and cardiovascular systems as well as autoimmune type 1 diabetes (T1D) [2, 3]. With respect to the treatment of diabetes with MSCs, some encouraging progress has been made. For example, intravenous injection of umbilical blood-derived allogeneic MSCs improved the function of pancreatic β-cells, reduced the incidence of diabetic complications, and led to insulin independence in some type 2 diabetic patients [4, 5]. Autologous MSCs were used to treat individuals with T1D and lead to the preservation of C-peptide . For this, bone marrow-derived MSCs were aspirated from iliac crest, a procedure with substantial discomfort . Moreover, the administration of bone marrow-derived allogeneic MSCs together with pancreatic islets enhanced islet survival in diabetic non-human primates . These studies employed fetal bovine serum in the MSC culture media, which is less desirable than media that lack animal proteins, pointing to a need for alternative culture and expansion strategies.
The mechanism by which MSCs protect human islets includes the expression of anti-inflammatory and pro-angiogenic genes [8, 9]. Tumor necrosis factor alpha-stimulated gene-6 (TSG-6) induced by TNF-α has anti-inflammatory properties [10, 11, 12]. Nuclear factor erythroid 2-related factor 2 (NRF2) is important in enhancing islet graft survival and function [13, 14]. Additionally, dimethyloxallyl glycine (DMOG), which targets prolyl-4-hydroxylase to prevent the degradation of hypoxia-inducible factor-1α  and upregulate vascular endothelial growth factor (VEGF) , could be a possible conditioning factor for improving MSC function.
MSCs have been isolated from various sites including subcutaneous adipose tissue [17, 18], bone marrow [19, 20], skeletal muscle , umbilical cord blood , ocular limbus , and amniotic fluid . Blood- and adipose-derived MSCs are widely investigated due to their accessibility, expandability, differentiability, and clinical applicability [25, 26]. During the enzymatic digestion of the cadaveric pancreas, cells are liberated, together with islets, which can then be separated and characterized. In this study, we isolated MSCs from the otherwise discarded fractions of pancreatic tissue. These cells, designated as intra-pancreatic tissue-derived (IPTD) MSCs, were cultured in a GMP-grade and xenoprotein-free culture medium containing human platelet lysate and conditioned in vitro with TNF-α  and DMOG. Changes in gene expression, growth factor, and cytokine levels and angiogenic capacity after conditioning were determined. This study identifies a previously unappreciated fraction of the pancreatic digest as a useful source of anti-inflammatory and pro-angiogenic MSCs with possible clinical applications.
Digestion of human pancreata from cadaveric donors
Characteristics of donors of pancreata used for islet and IPTD-MSC cell isolation
Cause of death
Mean ± SEM
33.8 ± 3.1
5.1 ± 0.1
29.8 ± 1.8
Intra-pancreatic tissue-derived cell harvesting and culture
To test our hypothesis that IPTD-MSCs can be separated from fractions of the pancreatic tissue, we modified our standard protocol, collected and pooled the upper layer found post-centrifugation, and passed the resultant through double layers of mesh filters (500 and 300 μm) to eliminate non-cellular components (Fig. 1). The filtered cells were then washed with CMRL-1066 culture medium and centrifuged at 727×g/8 °C for 3 min. The supernatant was aspirated, and the pellet was suspended in CMRL-1066 culture medium supplemented with 5% Human Platelet Lysate (hPL, Compass Biomed, MA) followed by transferring to a 50-mL conical tube. The suspended cells were centrifuged at 727×g/8 °C for 3 min. The supernatant was aspirated, and the pellet was suspended in 40 mL of CMRL-1066 medium containing 5% hPL followed by culturing in T-175 adherent flasks (ThermoFisher Scientific, Waltham, MA) for 24 h at 37 °C in 5% CO2 (Fig. 1). Twenty-four hours later, the medium was replaced with fresh CMRL-1066 medium containing 5% hPL. Additional media changes were performed every 48 h until cells reached ~ 80–90% confluence.
Bone marrow-derived MSCs
Bone marrow-derived human MSCs were obtained from healthy individuals as described [31, 32]. All subjects gave written informed consent in accordance with the Declaration of Helsinki. The study protocol was approved by the Medical Ethics Board of Leiden University Medical Center (LUMC).
Characterization of IPTD-MSCs
To record the growth and morphology of cultured cells, multiple pictures at different magnifications and time points were obtained using a ckx31 Olympus microscope.
After reaching 80–90% confluence, cells were dissociated with TrypLE (ThermoFisher, San Diego), washed with DPBS (Corning, Tewksbury, MA) twice, and incubated with antibodies specific for cell-surface molecules, including CD90, CD105, CD73, CD9, CD45, CD34, CD14, and HLA-DR (BioLegends, San Diego, CA), for 20 min at room temperature. In parallel, aliquots of cells were incubated with matched isotype control antibodies from the same supplier. After antibody incubation, cells were washed twice with DPBS and suspended in DPBS for flow cytometry analysis using a Sony SA3800 Spectral Analyzer (Sony Biotechnology, San Jose, CA). Data analysis was performed using Flowjo software (Tree Star, Ashland, OR). To verify the results, human bone marrow-derived MSCs were cultured in the same medium used for IPTD-MSCs, passaged, and expanded in the same procedures for subsequent analysis.
Immunofluorescent staining for IPTD-MSCs and pancreatic tissue
Cells were cultured to 70–80% confluence and dissociated into a single-cell suspension using TrypLE as described . Cells and pancreatic tissue were then fixed in 10% cold formalin, prepared in a paraffin block, and sectioned. Antigen retrieval was performed using a citric acid-based antigen unmasking solution (Vector, pH 6.0). Sections were treated with protein block (Biogenex, Fremont, CA) to reduce background signal, followed by incubation with mouse anti-CD105 antibody (ready to use; Biogenex) and ALEXA 488-conjugated goat anti-mouse IgG antibody (1:200 dilution; ThermoFisher). Guinea pig anti-insulin (ThermoFisher) and ALEXA 647-conjugated goat anti-Guinea pig IgG antibodies (1:200 dilution; ThermoFisher) were used for pancreatic tissue staining only. Fluoroshield™ containing DAPI (Sigma Aldrich St. Louis, MO) was used to stain nuclei. Image acquisition was done using an Observer Z1 microscope (Carl Zeiss), with the objective lens set at 20×. Image processing was done using the Zen 2.0 software.
Multilineage differentiation of IPTD-MSCs
IPTD-MSCs at the second passage were cultured in T-75 tissue culture flasks until ~ 85% confluence. For adipogenic differentiation, IPTD-MSCs were seeded into 6-well plates and cultured in MesenCult™ Adipogenic Differentiation Kit (STEMCELL Technologies, Vancouver, Canada; Cat# 05412) for 21 days with media changed every 3 days. The presence of lipid droplets in cells was determined by staining with Oil Red O (Sigma, cat# O0625) 21 days after culture. For chondrogenic differentiation, IPTD-MSCs were cultured in two 15-mL conical tubes in MesenCult™-ACF Chondrogenic Differentiation medium (STEMCELL Technologies, Cat# 05455) for 24 days with media changed every 3 days. After culture, Alcian Blue (Sigma, cat#66011) was used to stain for both fresh cells and the cells fixed in paraffin sections. For osteogenic differentiation, cells were cultured in a T-75 tissue culture flask for 22 days with media changed every 3 days. The osteogenic differentiation medium consisted of CMRL-1066 containing 10 mM β-glycerophosphate (Sigma, Cat# G-6251), 50 μg/mL l-ascorbate acid 2-phosphate (Cayman, Item # 16457), 1 μM of dexamethasone (Fresenius Kabi, Cat# 401780G), and 3% hPL. Differentiated cells were fixed in paraffin section and stained with von Kossa for calcium deposition. Undifferentiated IPTD-MSCs were cultured in standard culture medium lacking differentiation factors and stained with Oil Red O, Alcian Blue, or von Kossa.
In vitro expansion of IPTD-MSCs
T-175 flasks of ~ 80% confluent passage-3 cells were washed twice with DPBS, and 5 ml of TrypLE enzyme was added to each flask. The cells were incubated at 37 °C for 5–10 min to dissociate adherent cells, and 10 ml of CMRL-1066 medium was added to terminate enzyme digestion. Cells were collected in 15-ml tubes for centrifugation at 528×g for 3 min. The cell pellet was suspended in 5 ml CMRL-1066 with 5% hPL and vortexed. A sample of cells was mixed in a 1:1 ratio with 0.4% trypan blue (ThermoFisher), from which 20 μL was placed on a counting slide (Cellometer SD100, Nexcelom Bioscience, San Diego, CA) and counted using a Cellometer Auto T4 (Nexcelom Bioscience, San Diego, CA). To further characterize the growth capabilities of these cells, we performed subcultures by placing 5 × 104 cells in T-25 flasks for 72 h at 37 °C and 5% CO2. Some cells were grown in CMRL-1066 culture medium alone and others in CMRL-1066 culture medium supplemented with 5% hPL. Culture medium was replaced once during this period. At the end of the culture, cells were dissociated and counted as above. This process was then repeated. After each passage, the cell count was multiplied by the dilution factor to calculate the total number of cells per passage.
Cryopreservation of IPTD-MSCs
Isolated IPTD-MSCs (at passage 3) were cultured to ~ 80% confluence, dissociated into single cells with TrypLE, collected, and counted. Aliquots of 1 × 106 cells were divided into cryopreservation tubes, suspended in 10% DMSO in CMRL-1066 medium, and stored at − 80 °C in a Mr. Frosty Freezing apparatus containing 100% isopropyl alcohol (ThermoFisher). Using this method, IPTD-MSCs were stored for 9 months. The cells were then thawed rapidly in a 37 °C water bath, washed with DPBS, and cultured in T-75 tissue culture flasks using CMRL media with 5% hPL. After 48 h, the cells were noted to be ~ 80% confluent and were subjected to subsequent analyses. Viability was assessed with trypan blue.
In vitro treatment of IPTD-MSCs with TNF-α and DMOG
Recombinant human TNF-α protein (R&D Systems, Minneapolis, MN) was reconstituted in research-grade water (Hospira, Lake Forest, IL) to a concentration of 100 ng/mL, aliquoted, and stored at − 20 °C. Dimethyloxallyl glycine (DMOG; Cayman Chemicals, Ann Arbor, MI) was dissolved in water to yield a stock solution of 57.1 mM, aliquoted (100 μL), and stored at − 80 °C. IPTD-MSCs were incubated in T-25 flasks in 5 ml of CMRL-1066 medium supplemented with 5% hPL until ~ 50% confluent. Cells were cultured for 24 h in CMRL 1066 medium, or medium containing 10 ng/ml TNF-α, 1 mM DMOG or 1 mM DMOG and 10 ng/ml TNF-α. Following treatment, cells were collected in 1.7-ml Eppendorf tubes and stored in RLT buffer (Qiagen, Germantown, MD) at − 80 °C for future preparation of cDNA.
Quantitative real-time PCR
The TaqMan Gene Expression Assay system (ThermoFisher Scientific) was used to quantify β-ACTIN, TSG-6, NRF2, and VEGF mRNA levels. Total RNA was extracted using a Qiagen Mini Kit (Cat. No. 51306) and converted into cDNA. Real-time quantitative PCR was run in duplicate on a ViiA™ 7 Real-Time PCR System with a 384-well block (ThermoFisher Scientific). Thermal cycles were programmed for 20 s at 95 °C for the initial denaturation, followed by 45 cycles of 120 s at 95 °C for denaturation, 30 s at 60 °C for annealing, 60 s at 72 °C for extension, and a final extension at 72 °C for 10 min. All PCR runs were performed with negative (water) and positive controls. β-ACTIN was used as an internal control to quantify relative gene expression.
Supernatants from cells cultured for 24 h under various conditions (medium alone, or medium plus DMOG, TNF-α, or DMOG + TNF-α) were collected, and cytokine analysis performed using a Luminex assay kit (Bio-Rad, Hercules, CA) according to the manufacturer’s protocol. The following growth factors/cytokines were measured: VEGF, IL-6, IL-8, MMP-9, MCP-1, MMP-2, IL-4, IL-10, and IL-1β. Samples were measured in duplicate.
In vitro angiogenesis assay
Angiogenic capacity was assessed by quantifying endothelial tube formation . Human umbilical vein endothelial cells (HUVECs) (Cell Applications Inc., San Diego, CA; Cat# 200p-05n) between passages 2 and 6 were cultured in a standard medium. Cells (1 × 105 cells/well) were plated in 24-well plates (Fisher, Cat # 930186) coated with Matrigel (Corning, Cat# 356234), and incubated for 30 min to allow cell attachment. Supernatants (150 μL/well) from control and stimulated IPTD-MSCs (DMOG, TNF-α, or DMOG + TNF-α) were added to obtain a total volume of 300 μL per well. Plates were then incubated at 37 °C, 5% CO2 for 24 h. At 4 and 24 h, the wells were visualized using a Leica microscope and representative photographic images were obtained. Total endothelial tube number and tube length were determined using ImageJ software (NIH, Bethesda, MD).
Data was analyzed with GraphPad Prism software (GraphPad Software 8.0, La Jolla, CA). ANOVA one-way analysis of variance was used to compare multiple experimental groups followed by the Tukey multiple comparisons test to compare the mean values between any two groups. All the values were expressed as mean ± standard error of mean (SEM). For all the tests, p < 0.05 was considered significant.
A chemically defined medium supports the growth IPTD-MSCs
hPL is required for the growth of IPTD-MSCs
IPTD-MSCs display classic MSC cell-surface markers
IPTD-MSCs were passaged 3 times, dissociated into a single-cell suspension and stained with the above mentioned antibodies. Compared to isotype-control staining, the vast majority of IPTD-MSCs stained positive for CD90 (99.2 ± 0.3%), CD105 (99.8 ± 0.2%), CD73 (99.6 ± 0.3%), and CD9 (86.8 ± 2.6%) (Fig. 4a). Minimal expression of CD45 (0.3 ± 0.2%), CD34 (0.3 ± 0.0%), CD14 (1.5 ± 0.8%), and HLA-DR was found (Fig. 4a). Expression of CD105 on the cell surface of IPTD-MSCs at passages 3 and 5 was further visualized using immunofluorescent staining (Fig. 4b). Taken together, IPTD-MSCs expressed classic positive and lacked negative markers for MSCs, suggesting that they reside within the MSC family of cells.
CD105+ cells localize in the pancreas near insulin-expressing cells
IPTD-MSCs have potential to differentiate into multiple cell lineages in vitro
TNF-α and DMOG upregulate immune-regulatory and angiogenic genes in IPTD-MSCs
TNF-α and DMOG alter growth factors and cytokines released by IPTD-MSCs
Conditioned medium from IPTD-MSCs stimulated with DMOG promotes angiogenic activity of endothelial cells
We identified a MSC population that resides within pancreatic tissues, which can be separated during islet isolation. We named these cells intra-pancreatic tissue-derived (IPTD)-MSCs, in agreement with the recent call for nomenclature of MSCs in relation to their tissue of origin [37, 38, 39]. In culture, IPTD-MSCs displayed features similar to classic bone marrow- or umbilical cord blood-derived MSCs, including adherence to culture-grade plastic surfaces, spindle-shaped morphology, expression of appropriate surface markers (positive for CD90, CD105, and CD73, and negative for CD45, CD34, CD14 and HLA-DR), and capacity for proliferation and multilineage differentiation. Furthermore, when IPTD-MSCs were treated with a combination of TNF-α and DMOG, we observed (1) increased mRNA levels of TSG-6, NRF2, and VEGF; (2) increased secretion from IPTD-MSCs of VEGF, IL-6, IL-8, and IL-4; (3) decreased secretion of MCP-1; and (4) enhanced endothelial cell tube formation. Together, these results suggest IPTD-MSCs conditioned by TNF-α and DMOG have anti-inflammatory and pro-angiogenic potential.
The cell population, isolation, and culture method of IPTD-MSCs we described herein have both differences and similarities over other previously published MSCs . In this study, cells were isolated from intra-pancreatic tissue as a part of islet isolation procedure from a single donor. IPTD-MSCs were harvested from an otherwise discarded component after routine pancreatic digestion and islet isolation. The GMP-compatible protocol used for culturing these cells led to the production of large numbers of highly purified MSCs. We deliberately selected CMRL-1066 as the base medium to propagate IPTD-MSCs because CMRL-1066 is routinely used to culture islets for transplantation, thus reducing the burden for future clinical translation. Additionally, we eliminated animal products in culture media by using hPL, which will lower the risks of infection, allergic reactions, and product variability. Similar to MSCs derived from other tissue sources, IPTD-MSCs are capable of differentiation into adipocyte, chondrocyte, and osteoblast lineages, demonstrating the multi-lineage potential of IPTD-MSCs.
This study demonstrates an approach that allows for harvesting islets and IPTD-MSCs simultaneously from a single donor under GMP conditions, facilitating direct clinical application. Harvesting IPTD-MSCs during human islet isolation makes the quality evaluation of isolated cells rapid and reliable and suggests opportunities for immediate clinical applications. Previously, autologous bone marrow-derived MSCs have been used simultaneously in living-related kidney transplant recipients . Moreover, we expanded bone marrow-derived MSCs in the same medium of CMRL-1066 supplemented with hPL and found that these MSCs were similar in phenotype and characteristics compared to IPTD-MSCs, suggesting that our medium could be used to isolate MSCs from other tissue sources. IPTD-MSC culture medium used in this study is xenoprotein-free and cGMP-compatible. The isolated IPTD-MSCs were expandable and can be produced in large scale using this culture medium. Conventionally, fetal bovine serum is supplemented in selected culture media to promote the growth of MSCs from different tissue sources . However, the use of non-human serum to culture cells carries the potential of transmitting infectious agents , immunizing effects , and lot-to-lot variability. In this regard, human platelet lysate has been used to replace fetal bovine serum for clinical-scale MSC expansion . In these studies, hPL was supplemented in minimal essential medium (MEM) to culture MSCs. In the current study, we used hPL to supplement the CMRL-1066 that has been optimized for human islets culture, and the culture system employed herein allows for optimum survival of IPTD-MSCs. This is important since a single medium system can be used for both cell sources to facilitate co-transplantation of islets and IPTD-MSCs in future studies.
This study also highlights the benefit of harvesting multiple cell types from tissue fractions of a single donor organ as part of the islet isolation procedure. It is conceivable that immunophenotypic characterization and identification of additional novel cell types residing within this tissue fraction would be valuable to study pancreatic pathophysiology arising from various diseases.
MSCs are known to reduce inflammation and enhance healing, and these functions can be further manipulated ex vivo to enhance capacities for cell therapies. Compared to control, we found that IPTD-MSCs exposed to a combination of TNF-α and DMOG, compared to single reagents, exerted a better overall outcome. Except for TSG-6 expression, no other molecules, including the secreted factors examined in this study, were affected by TNF-α treatment alone. In contrast, DMOG alone was able to induce NRF2, VEGF expression, as well as the secretion of VEGF, IL-6, IL-8, and IL-4. These results demonstrate a dominant effect of DMOG over TNF-α. However, TNF-α was able to augment the effects brought by DMOG in increasing the expression of TSG-6, NRF2, and VEGF and enhancing secretion from IPTD-MSCs of IL-6, IL-8, and IL-4. Regardless, the combination of TNF-α and DMOG appeared to be optimal for the examined outcomes, including the expression of TSG-6, NRF2, and VEGF; secretion of VEGF, IL-6, IL-8, and IL-4; and endothelial tube formation. To the best of our knowledge, this is the first study to show a beneficial effect on MSCs by conditioning with the combination of TNF-α and DMOG.
IL-4 levels were significantly increased by the combination of DMOG and TNF-α as compared to the control or DMOG alone, whereas IL-10 production was unchanged. This is in line with previous reports demonstrating that MSCs do not secrete IL-10, but stimulate other immune cells to secrete this cytokine . MCP-1 (monocyte chemoattractant protein-1) is often increased upon treatment with inflammatory cytokines. We found that treatment of IPTD-MSCs with DMOG and TNF-α led to a reduction of MCP-1. Taken together, our results show the production of anti-inflammatory molecules in IPTD-MSCs. It remains to be determined if these human cells will provide protection in inflammatory settings.
VEGF, IL-6, IL-8, and MMP-9 are known pro-angiogenic factors [47, 48, 49, 50, 51], which may be responsible for the observed enhancement of endothelial cell tube formation. Upregulation and secretion of pro-angiogenic factors are important for several reasons: (i) MSCs from individuals with diabetes showed lowered angiogenic capacity  than those from individuals without diabetes, although another study reported that MSCs isolated from the bone marrow of T1D donors were phenotypically and functionally similar to those isolated from healthy individuals ; (ii) treatment of islets with the iron chelator deferoxamine stabilized HIF-α and enhanced islet VEGF levels ; and (iii) treatment with exogenous VEGF improves islet engraftment  and β-cell mass , in part through increased angiogenesis. Islet survival and function post-transplantation are adversely impacted by hypoxia . Thus, processes that render islets hypoxia-resistant, such as increasing VEGF expression and secretion, should have beneficial effects in islet transplantation. The fact that the combination of DMOG and TNF-α also enhances TSG-6, NRF2, and VEGF gene expression from bone marrow-derived MSCs highlights the potential use of DMOG and TNF-α to condition MSCs other than IPTD-MSCs. Further, the upregulation of TSG-6 in both IPTD-MSCs and bone marrow-derived MSCs underscores the concept of employing TSG-6 as a marker of anti-inflammatory capacity .
An interesting finding was the proximity of MSCs to islets within the pancreatic tissue, implying a possible role for these MSCs in protecting islets from metabolic stress and inflammation. Besides the potential anti-inflammatory and pro-angiogenic effects of IPTD-MSCs, future studies will explore whether extracellular vesicles (EV)  secreted by these cells are more effective at limiting autoimmune diseases such as T1D and uveoretinitis .
In summary, the simultaneous isolation of human islets and intra-pancreatic tissue-derived MSCs was demonstrated. These IPTD-MSCs can be expanded in a clinically applicable culture system and potentiated ex vivo in their anti-inflammatory and pro-angiogenic properties. Such IPTD-MSCs, together with the islets originating from the same donor organ, may enhance islet transplantation outcome and other potential clinical applications.
Human pancreatic islets were provided by the NIDDK-funded Integrated Islet Distribution Program (IIDP) at City of Hope. The authors gratefully acknowledge Ms. Kiran Sriram and Dr. Zhen Chen for technical assistance with the Matrigel tube formation assay. We also extend our thanks to all islet isolation team members at City of Hope. Luminex assays of culture supernatants were performed by staff members of the core facility at the Beckman Research Institute of City of Hope.
BK conducted the experiments; collected, analyzed, and interpreted the data; and wrote the manuscript. MQ and IHA conceived and designed the study; collected and or assembled, analyzed, and interpreted the data; and wrote the manuscript. WD, KTC, KVM, and RGP conducted the experiments and collected the data. JSI analyzed and interpreted the data and wrote the manuscript. FK provided the financial support for the study. HTK performed the data analysis and interpretation and wrote the manuscript. All authors read and approved the final manuscript.
This study was supported, in part, by the Diabetes and Metabolic Research Institute of City of Hope to F.K. and NIH grant R01DK099734 to H.T.K. Support from the Wanek Family Project of Type 1 Diabetes to F.K. and H.T.K. is also gratefully acknowledged.
Ethics approval and consent to participate
Research consent for the use of human tissue was obtained from the donor next of kin and ethics approval for this study was granted by the Institutional Review Board of City of Hope (IRB # 01046). In the case of bone marrow-derived MSCs, consent was obtained from donors and ethics approval for this was granted by the Medical Ethics Board of Leiden University Medical Center.
Consent for publication
BK, MQ, HTK, and IHA have patents pending related to this study. The other authors declare that they have no competing interests.
- 14.Yagishita Y, Uruno A, Chartoumpekis DV, et al. Nrf2 represses the onset of type 1 diabetes in non-obese diabetic mice. J Endocrinol. 2019;240(3):403–416.Google Scholar
- 20.Kayleigh M. Van Megen E-JvtW, Julia Lages Motta, Bernice Dekker, Tatjana Nikolic, Bart O. Roep. Activated mesenchymal stromal cells process and present antigens regulating adaptive immunity. Front Immunol doi: https://doi.org/10.3389/fimmu.2019.00694 (in press).
- 39.Zazzeroni L, Lanzoni G, Pasquinelli G, et al. Considerations on the harvesting site and donor derivation for mesenchymal stem cells-based strategies for diabetes. CellR4 Repair Replace Regen Reprogram; 2017. p. 5.Google Scholar
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