The impact of the mTOR inhibitor sirolimus on the proliferation and function of pancreatic islets and ductal cells
- 760 Downloads
The Edmonton Protocol for islet transplantation has provided hope for type 1 diabetic patients. However, this protocol requires lifelong immunosuppression, specifically sirolimus, a cellular antiproliferate. The effect of sirolimus on human pancreatic ductal cells (HDCs) is not known. This may be important since HDCs are believed to be islet precursors. Since neonatal porcine islets (NPIs), which contain many ductal precursor cells, could be a potential clinical source of islets, we also tested the effects of sirolimus on this tissue.
HDCs (n=4), NPIs (n=9) and human islets (n=5) were cultured with and without sirolimus (20 ng/ml) for 6 days.
HDCs and NPIs cultured with sirolimus showed a 50 and 28% decrease, respectively, in cell number relative to control (p<0.05). Control cultures expanded 1.65- and 2.44-fold relative to time 0. Decreases in cell number of sirolimus-treated HDCs were not due to apoptosis as measured by TUNEL staining. No functional effects on human islets or NPIs were observed following static incubation with high glucose. Treatment of syngeneically transplanted and naïve BALC/c mice with sirolimus resulted in altered OGTT profiles with prolonged elevation of hyperglycaemia and weight gain. There was no difference in graft and organ insulin content between treatment groups.
Our results indicate that sirolimus decreases ductal cell numbers in culture and alters glucose-stimulated insulin secretion in vivo. The administration of sirolimus to islet transplant recipients is likely to impair graft function as a result of decreasing ductal neogenesis and induction of insulin resistance.
KeywordsDuctal cell Human islet Neonatal porcine islet Sirolimus
glucose-stimulated insulin secretion
Hanks’ balanced salt solution
human pancreatic ductal cell
mammalian Target Of Rapamycin
neonatal porcine islet
TdT-mediated dUTP nick-end labelling
The clinical success of islet transplantation has provided an effective treatment for type 1 diabetic patients [1, 2]. Key elements for this success are the immunosuppressive protocol and transplantation of sufficient islet cell mass. Sirolimus, tacrolimus, and daclizumab are administered to transplant recipients to prevent islet graft rejection . While this cocktail is free of steroidal drugs, which are known to have diabetogenic side effects , these agents may still affect the long-term function and survival of human islet grafts.
Several studies have investigated the effects of these immunosuppressive agents on beta cell function in human cell lines , rodent beta cells  and human beta cells [6, 7, 8]. These studies have shown that high doses of tacrolimus and sirolimus can cause significant exocytosis of cellular insulin , inhibition of insulin secretion upon stimulation by glucose [5, 8] and induction of apoptosis in both beta and alpha cells . A recent clinical update of patients with long-term islet grafts shows that graft function diminishes over a 5-year period , necessitating exogenous insulin administration for the maintenance of tight glycaemic control. Graft function as demonstrated by persistent C-peptide secretion is maintained, but the amount of insulin generated by the graft is no longer sufficient to maintain euglycaemia in the absence of usually small amounts of supplemental injected insulin. This reduction in insulin production may be the result of beta cell death coupled with impaired beta cell regeneration.
Finegood et al.  reported that the average life span of a beta cell is 1 to 3 months. Therefore dynamic beta cell turnover occurs within the pancreas to maintain a critical mass of functional beta cells. This also suggests that beta cell turnover occurs within islet grafts to maintain long-term function after transplantation. The source of pancreatic beta cell progenitor cells remains unknown. Using a genetic lineage tracing approach, Dor et al. reported that adult pancreatic beta cells are formed by self-duplication rather than differentiation from an undifferentiated stem cell . Others have suggested that pancreatic ductal cells can serve as multipotent progenitor cells and that external stimuli can direct the differentiation of these cells to endocrine, acinar, or mature ductal cell phenotypes [11, 12, 13, 14, 15]. Other investigators have shown that the population of bone marrow or spleen cells may contain stem cells that can differentiate into beta cells [16, 17, 18].
The working hypothesis of our group is that ductal cells are the beta cell progenitors within the pancreas, contributing via neogenesis to the generation of new beta cells. We have recently shown that islet recipients who receive greater numbers of ductal cells within islet grafts have better graft function at 2 years post transplant as measured by acute insulin response to glucose . Since ductal progenitors within the grafts may contribute to long-term graft function, it is important to determine the effect of immunosuppressive agents on these cells. Indeed, long-term immunosuppression may reduce graft function either by direct drug effects on the beta cells themselves or by effects on ductal cell progenitors that are transplanted with the islets (ductal cells form 20–30% of islet grafts) .
Sirolimus is a non-specific antiproliferative drug administered to patients receiving islet grafts. Sirolimus inhibits the clonal expansion of activated lymphocytes by interacting with the mammalian target of rapamycin (mTOR), inhibiting progression from the G1 to the S phase of the cell cycle . Since the proteins bound by sirolimus are not unique to T cells, it is possible that sirolimus exerts this antiproliferative effect on other cell types. Studies have shown that sirolimus inhibits proliferation of coronary artery smooth muscles, hepatic stellate cells, small lung cancer cells, mouse proximal tubular cells and pancreatic cancer cells [21, 22, 23, 24, 25]. If sirolimus inhibits the proliferation of pancreatic duct cells or even existing beta cells within the islet grafts, this drug may impede new beta cell formation and thus limit graft longevity and function.
In the present study we have evaluated the effect of sirolimus on the function and proliferation of human pancreatic ductal cells (HDCs) and human islet cells. We have also tested the effects of sirolimus on neonatal porcine islets (NPIs). NPIs constitute a potential source of cells for clinical transplantation because of their inherent ability for proliferation and differentiation . Recently, we provided the first evidence that allogeneic NPIs can reverse diabetes in a large animal model [27, 28].
Materials and methods
All experimental protocols used in this study were approved by the Research Ethics Board of the University of Alberta.
Human pancreases were removed from cadaveric donors, who had previously given informed consent, and processed according to previously described protocols . Briefly, pancreata were stored in chilled University of Wisconsin solution before islet isolation. Islet isolation, gradient purification and tissue collection was performed as previously described for human islets [2, 30]. For the in vitro insulin secretion experiments fresh (n=3) or cryopreserved (n=2) (donor ages 24–64 years) human islets were cultured in non-tissue-culture-treated plates for 2 to 3 days with RPMI 1640 medium (Gibco/Invitrogen, Burlington, ON, Canada) + insulin–transferrin–selenium (ITS)/BSA with 10% FCS prior to experimentation.
Following islet purification, the ductal/acinar fraction was collected and washed three times with Hanks’ balanced salt solution (HBSS; Mediatech Sigma-Aldrich, Oakville, ON, Canada) supplemented with 0.5% BSA (fraction V; Sigma). This fraction (n=4; donor ages 11–67 years) was cultured in suspension for 4 to 6 days with RPMI 1640 medium supplemented with 1% ITS/0.5% BSA. Medium was exchanged at day 1 post culture and every 2 days thereafter. At the end of the culture period these preparations are composed of 68% cytokeratin (CK)-19, 16% amylase, and 1% beta cells .
The isolation method for NPIs has been described . Briefly, pancreases from Landrace–Yorkshire neonatal pigs (1–3 days old, 1.5–2.0 kg body weight) were removed and digested in 2.5 mg/ml of collagenase (Sigma). After filtration (500 μm), cells were cultured for 6 days in HAMs F10 medium (Gibco) containing 10 mmol/l glucose, 50 μm isobutylmethylxanthine (ICN Biomedicals, Montreal, QC, Canada),0.5% BSA, 2 mmol/l l-glutamine,10 mmol/l nicotinamide (BDH Biochemical, Poole, UK), 100 IU/ml penicillin, and 100 μg/ml streptomycin. The medium was replaced every second day. After this culture period, the NPIs are routinely composed of 35% endocrine and 57% ductal endocrine precursor (CK7-positive) cells .
Islets were isolated from BALB/c mice (purchased from The Jackson Laboratory, Bar Harbor, ME, USA); pancreases were distended with collagenase solution (1 mg/ml), surgically removed and digested. Following dextran gradient centrifugation, islets were picked off gradient interfaces, washed with HBSS and cultured overnight in Hams F10 .
Cell expansion and characterisation
After isolation and 4 to 6 days of culture  HDCs were cultured at ∼1.5×105 cells/well with and without 10 or 20 ng/ml sirolimus (Rapamune; Wyeth-Canada Laboratories, Markham, ON, Canada). NPIs (535 aggregates/well) were cultured as experimental cultures with 20 ng/ml of sirolimus added to the base media or as control cultures grown in base media alone. All cells were cultured in 12-well tissue-culture-treated plates with RPMI 1640 (Gibco) and HEPES buffer, sodium pyruvate, 100 IU/ml penicillin, 100 μg/ml streptomycin, 10% FBS, 2-beta-mercaptoethanol and 20 ng/ml endothelial growth factor and basic fibroblast growth factor (Invitrogen) to induce cell proliferation. Cell preparations were assessed for cell number by measuring DNA content at time 0 and day 6 of culture. We have previously shown that human islet cells contain 6.6 pg DNA/cell  whereas NPI cells have 7.1 pg DNA/cell . Cellular insulin content and cellular composition of the NPI cultures were also characterised at these timepoints.
To determine cell number, aliquots of the cell suspension were measured in triplicate for total cellular DNA content using a fluorometric assay (Hoefer DyNa Quant 200; Amersham Pharmacia Biotech, San Francisco, CA, USA) as described previously . Insulin content was measured after cellular extraction by RIA (porcine) or by ELISA (human) .
The cellular composition of NPI and HDC cultures was determined by immunohistochemistry using the avidin–biotin complex–3,3 diaminobenzidinetetrahydrochloride method. Briefly, cellular aggregates were dissociated into single cell suspensions and adhered to histobond slides (Marienfeld Glassware, Bad Mergentheim, Germany). Slides were fixed in Bouin’s fixative for 12 min before storage at 4°C in 70% ethanol. Cells were quenched with 20% H2O2/methanol followed by microwave antigen retrieval for CK 7 and 19 in sodium citrate. Primary antibody concentrations were as follows: 1/1,000 guinea pig anti-porcine insulin (Dako, Glostrup, Denmark), 1/50 mouse anti-human CK19 (Dako), 1/200 mouse anti-human CK7 (Dako). Antibodies to CK7 and 19 were used as markers for pancreatic ductal epithelial-type cells as previously described . All biotinylated secondary antibodies were obtained from Vector Laboratories (Burlingame, CA, USA) and used at a concentration of 1/200. Single cell counts were performed on 500 cells per sample and percentages calculated.
Apoptosis in control and sirolimus-treated HDCs was quantified using TdT-mediated dUTP nick-end labelling (TUNEL) staining. Single cells were adhered to histobond slides and fixed as described above. Cells were stained for CK19 to identify ductal cells using mouse anti-human CK19 (1:25; Dako) and labelled using Cy3-conjugated anti-mouse IgG (Jackson Immunoresearch Laboratories, West Grove, PA, USA). Next, the apoptotic nuclei were labelled with fluorescein isothiocyanate-dUTP (Roche, Laval, Quebec, Canada) using the TdT enzyme (Deadend Fluorometric TUNEL System; Promega, Madison, WI, USA). The stained slides were analysed using fluorescent microscopy and cells were counted as described above.
Islet secretory activity
Human islets and NPIs were suspension-cultured in 79-cm2 dishes with 10 ml of RPMI + ITS/BSA, 10% FCS (human islets) or Hams F10 (NPIs), with 20 ng/ml of sirolimus included in experimental cultures. Control samples were cultured in base media. All cultures were maintained at 37°C (5% CO2, 95% air) in humidified air for 6 days, with medium changed every second day. Samples were taken at day 0 and day 6 for analysis of DNA and insulin content, glucose-stimulated insulin secretion (GSIS) and immunohistochemical composition.
Human islet and NPI secretory response to glucose were determined using static incubation assay . Islet cell aliquots were washed with Hams F10 media without glucose and incubated for 120 min in 1.5 ml of Hams media with either 2.8 or 20 mmol/l glucose. The supernatant was then sampled and assayed for insulin using ELISA (human) or RIA (porcine). The insulin content of the supernatant was expressed as a percentage of the total content (i.e. tissue plus medium). Stimulation indices were calculated by dividing the amount of insulin released at 20 mmol/l glucose by that released at 2.8 mmol/l glucose .
In vivo studies
Effect of sirolimus on mouse islet graft function
We transplanted 500 mouse islets that had been cultured for 1 day under the left kidney capsule of halothane-anaesthetised diabetic BALB/c mice (The Jackson Laboratory). Diabetes (glycaemia >8.4 mmol/l) was induced using 275 mg/kg body weight of streptozotocin (Sigma) injected intraperitoneally 2 days prior to transplantation. Transplanted mice were randomly separated into two groups control (untreated) and experimental (sirolimus-treated). Sirolimus treatment consisted of daily i.p. injection of 0.2 mg/kg sirolimus commencing the day after transplant and continuing for 26 days. Blood glucose levels were monitored weekly between 08:00 and 11:00 hours. An OGTT  was performed 48 h prior to graft removal on recipients that had achieved normoglycaemia (blood glucose ≤8.4 mmol/l). After a 6-h fast, a bolus of 50% dextrose (3 mg/g body weight) was administered intragastrically to non-anaesthetised mice. Tail vein blood samples were obtained at 0, 15, 30, 60, 90 and 120 min. Nephrectomy of the graft-bearing kidney was performed and the insulin content of the graft was determined after organ extraction by RIA.
Effect of sirolimus on native pancreatic islet function
Naïve BALB/c mice were divided into control (n=11) and experimental (n=11) groups. Experimental animals received a daily i.p. injection of sirolimus (0.2 mg/kg) for 26 days as detailed above and control animals received daily injections of saline. Blood glucose was monitored weekly and OGTT tests were performed at day 26 to assess pancreatic islet function. Pancreases were removed 48 h post-OGTT and organs assayed for insulin content. In a subset of animals (n=4), whole blood was collected post-OGTT into EDTA-treated tubes via cardiac puncture and sirolimus content was measured by RIA.
Data are expressed as mean±SEM of n independent observations. Statistical significance was calculated with a two-tailed unpaired Student’s t test or a one-way ANOVA in the case of multiple comparisons.
Sirolimus inhibits proliferation of human pancreatic ductal cells and NPIs
The effect of sirolimus on the fold expansion and cellular composition of neonatal porcine islets
Positive cells %
Sirolimus does not alter in vitro function of human islets or NPIs
Effect of sirolimus on glucose-stimulated insulin secretion of human islets and NPIs
Insulin secretion (% content)
2.8 mmol/l glucose
20 mmol/l glucose
The insulin secretory activity of NPIs cultured for 6 days in suspension with medium containing 20 ng/ml sirolimus was not different from controls (Table 2). Stimulation indices of control and sirolimus-treated cultures were 3.01±0.86 and 1.98±0.33, respectively, which was not statistically different from time 0 values of 1.96±0.34.
Sirolimus impairs the function of syngeneic BALB/c mouse islet grafts and innate pancreatic islets
Prior to this study the effect of sirolimus on pancreatic ductal cell proliferation was not known. We have evaluated the effect of sirolimus on ductal cell expansion, islet function and the in vivo function of islet grafts and pancreas. We found that in HDCs and NPIs, which contain 57% ductal cells, cell expansion was inhibited by 50 and 33%, respectively, relative to untreated controls. These results are not surprising since sirolimus interacts with the FK506 binding protein intracellular binding proteins. The sirolimus–FK506 binding protein complex binds directly with mTOR and blocks its function. By inhibiting mTOR function, the protein translation necessary for cell growth and proliferation is inhibited and sirolimus halts the cell cycle in the G1 phase . We observed that porcine ductal cells are more resilient to sirolimus than HDCs, a finding of clinical importance for xenotransplantation. If porcine tissue shows enhanced resilience to the negative effects of immunosuppressive drugs such as sirolimus, the graft longevity of porcine cells may be enhanced compared with human cell equivalents.
We found that sirolimus-treated HDCs did not show increased apoptosis relative to controls following 6 days of drug treatment. Although we did not culture our cells with [3H] thymidine, it has been shown that in human preadipocytes sirolimus inhibits proliferation as measured by this method . The absence of elevated apoptosis in our study, coupled with the absence of proliferation reported by others , suggests that the decreased cell number within our sirolimus-treated cultures is probably primarily due to an inhibition of ductal proliferation. When HDCs were cultured with sirolimus, cell viability decreased to below that of time 0 (Fig. 1), indicating that sirolimus treatment induced cellular toxicity possibly by an early induction of apoptosis or necrotic cell death prior to day 6, and thus was not detected when we assessed our cultures at day 6. In addition to its anti-proliferative properties, sirolimus has been shown by others to exhibit cellular toxicity, with a reduction of islet viability as measured by MTT and Calcein assay occurring at high concentrations (100 ng/ml) .
Clinically, patients receiving higher numbers of ductal cells have better long-term graft function despite sirolimus treatment, indicating that the high number of ductal cells present in islet grafts is sufficient to overcome the antiproliferative effects of sirolimus. However, sustained treatment with sirolimus may have an antiproliferative effect that is sufficient to diminish graft function as observed over time .
To study the systemic effects of sirolimus, mouse islets were transplanted beneath the kidney capsule of diabetic BALB/c mice. Sirolimus-induced changes were observed in the OGTT profile, with mice showing elevated blood glycaemia during the glucose challenge followed by a return of levels to normal by the end of the test period.
The observed differences in OGTT profile may be due to poor vasculature caused by inhibition of angiogenesis, altered islet function resulting from ectopic transplantation, inhibition of islet function or reduced ductal proliferation. To determine if differences were due to poor vasculature or ectopic site, we treated naïve mice with daily injections of sirolimus. These mice had normal daily blood glucose, but also showed exacerbated changes in blood glucose regulation upon OGTT testing. The sirolimus content of whole blood from these mice was 37.03±4.0 ng/ml, which is higher than the initial trough target levels of 10 to 12 ng/kg in human islet transplant recipients. We feel, however, that the high levels of sirolimus to which the animals are exposed may accurately represent the high peak drug concentrations within the portal circulation, to which human and large animal islet grafts are exposed after being infused into the recipient liver . Similar decreases in insulin response to glucose have been reported in an allograft porcine model of islet transplantation and in the clinical setting of patients who receive islet transplantation [27, 38]. In both reports transplant recipients received sirolimus as part of their immunosuppressive regime and demonstrated elevated glucose following a glucose challenge test.
The sustained hyperglycaemia observed during OGTT testing, together with increased weight gain in sirolimus-treated animals, suggests the initiation of insulin resistance in these animals. Sirolimus decreases the phosphorylation of serine 307 on IRS-1 in adipocytes, thereby inhibiting efficient insulin signalling in human adipocytes and mimicking what is seen with type 2 diabetes . In our work we did not observe any effect on GSIS in human or porcine islets exposed to sirolimus in vitro. However, altered OGTT profiles were observed in vivo when sirolimus was administered to naïve mice and diabetic mice transplanted with syngeneic islet grafts. It is likely that sustained hyperglycaemia during OGTT testing resulted from an inhibition of efficient signalling in the adipocyte, leading to decreased efficiency of insulin-induced glucose sequestration by the adipocyte. It is also known that sirolimus inhibits insulin-induced synthesis of glycogen and protein in muscle [40, 41], which may also contribute to the sustained hyperglycaemia observed by us in vivo but not in vitro upon hyperglycaemic challenge.
This study presents convincing evidence that sirolimus inhibits the proliferation of pancreatic ductal cells and alters GSIS in vivo. Therefore, by administering sirolimus to islet transplant recipients, we are probably inhibiting long-term graft function by decreasing ductal neogenesis and inducing insulin resistance. Future work in this area will include the investigation of new immunosuppressive drugs and tolerance induction protocols to replace the use of sirolimus for effective immunosuppression. Indeed, there are many promising new drugs, such as sphingosine-1-phosphate receptor agonists or the costimulation inhibitor belatacept, which are now undergoing clinical trial and which may provide specific T cell inhibition with fewer diabetogenic side effects [42, 43].
C. T. Bussiere is supported in part by a grant from the Stem Cell Network (Canadian Centres of Excellence). J. R. T. Lakey and G. S. Korbutt are recipients of scholarships from the Canadian Diabetes Association as well as the Alberta Heritage Foundation for Medical Research. G. S. Korbutt also has a Career Development Award from the Juvenile Diabetes Research Foundation. A. M. J. Shapiro is a clinical investigator of the Alberta Heritage Foundation for Medical Research and holds the Clinical Research Chair in Transplantation (CIHR/Wyeth). Funding for this project was provided by grants from the Alberta Foundation for Diabetes Research, Juvenile Diabetes Research Foundation, and the Canadian Institute for Health Research.
The authors thank D. Colwell for assistance with figures and formatting as well as M. McCammon, E. Henry, L. Elder, K. Seeburger and J. Lyon for technical assistance and data collection. They also thank the staff of the Clinical Islet Laboratory (University of Alberta) and the H.O.P.E. program for identifying and procuring organs from cadaveric donors.