Mesenchymal stromal cell secretory molecules improve the functional survival of human islets

Abstract

AimsHuman islet transplantation as a therapy for type 1 diabetes is compromised by the loss of functional beta cells in the immediate post‐transplantation period. Mesenchymal stromal cells (MSCs) and MSC‐derived secretory peptides improve the outcomes of islet transplantation in rodent models of diabetes. Here we utilized a mouse model for human islet transplantation and assessed the effects of a cocktail of MSC‐secreted peptides (screened by MSC‐secretome for human islet GPCRs) on the functional survival of human islets.MethodsHuman islets from 9 donors (Age: 36‐57; BMI: 20‐35) were treated with a cocktail of human recombinant annexin A1 (ANXA1), stromal cell‐derived factor‐1 (SDF‐1/CXCL12) and complement component C3 (C3a). Glucose stimulated insulin secretion (GSIS) was assessed in static incubation and cytokine‐induced apoptosis was assessed by measuring caspase 3/7 activity. mRNA expression levels were determined by qPCR. Human islet function in vivo was assessed using a novel model for human islet transplantation into a T1D mouse model. Human islet function in vivo was assessed using islet transplantation under the kidney capsule of immunodeficient mice prior to STZ destruction of endogenous mouse beta cells to model T1DM.ResultsPre‐treatment with a cocktail of MSC‐secreted peptides increased GSIS in vitro and protected against cytokine‐induced apoptosis in human islets isolated from nine donors. Animals transplanted with either treated or untreated human islets remained normoglycemic for up to 28 days after STZ‐administration to ablate the endogenous mouse beta cells, whereas non‐transplanted animals showed significantly increased blood glucose immediately after STZ administration. Removal of the human islet graft by nephrectomy resulted in rapid increases in blood glucose to similar levels as the non‐transplanted controls. Pre‐treating human islets with the MSC‐derived cocktail significantly improved glucose tolerance in graft recipients, consistent with enhanced functional survival of the treated islets in vivo.ConclusionPre‐treating human islets before transplantation with a defined cocktail of MSC‐derived molecules could be employed to improve the quality of human islets for transplantation therapy for type 1 diabetes.

Basic science lays the foundation to success

“…These informative articles cover a range of topics including the genetic evidence for distinct biological mechanisms that link adiposity to type 2 diabetes, 8 mechanisms of long-chain free fatty acid uptake into beta cells, 9 comparison of the effectiveness of fluorescent microparticle delivery to mouse liver through the hepatic portal vein via open laparotomy or ultrasound guidance, 10 and the use of mesenchymal stromal cells in improving transplanted human islet survival. 11 We are delighted by the quality and breadth of these basic science articles in this special issue: the future looks bright for diabetes research in the UK.…”