Mesenchymal Stem Cells and Islet Cotransplantation in Diabetic Rats: Improved Islet Graft Revascularization and Function by Human Adipose Tissue-Derived Stem Cells Preconditioned with Natural Molecules

Author:

Cavallari Giuseppe12,Olivi Elena345,Bianchi Francesca45,Neri Flavia12,Foroni Laura3,Valente Sabrina6,La Manna Gaetano7,Nardo Bruno12,Stefoni Sergio7,Ventura Carlo45

Affiliation:

1. Department of General Surgery and Transplantation, University of Bologna, Bologna, Italy

2. Center for Applied Biomedical Research (CRBA), University of Bologna, Bologna, Italy

3. Department of Specialistic Surgery and Anaesthesiological Sciences, University of Bologna, Bologna, Italy

4. Cardiovascular Department, University of Bologna, Bologna, Italy

5. Laboratory of Molecular Biology and Stem Cell Engineering - National Institute of Biostructures and Biosystems (NIBB), Bologna, Italy

6. Department of Hematology, Oncology and Laboratory Medicine, University of Bologna, Bologna, Italy

7. Nephrology, Dialysis and Renal Transplant Unit, S. Orsola - Malpighi Hospital, University of Bologna, Bologna, Italy

Abstract

Hypoxia plays an important role in limiting the engraftment, survival, and function of intrahepatically transplanted islets. Mesenchymal stem cells (MSCs) were recently used in animal models of islet transplantation not only to reduce allograft rejection but also to promote revascularization. Among different possible origins, adipose tissue represents a novel and good source of MSCs. Moreover, the capability of adipose tissue-derived stem cells (ASCs) to improve islet graft revascularization was recently reported after hybrid transplantation in mice. Within this context, we have previously shown that hyaluronan esters of butyric and retinoic acids can significantly enhance the rescuing potential of human MSCs (hMSCs). Here we evaluated whether ex vivo preconditioning of human ASCs (hASCs) with a mixture of hyaluronic (HA), butyric (BU), and retinoic (RA) acids may result in optimization of graft revascularization after islet/stem cell intrahepatic cotransplantation in syngeneic diabetic rats. We demonstrated that hASCs exposed to the mixture of molecules are able to increase the secretion of vascular endothelial growth factor (VEGF) as well as the transcription of angiogenic genes, including VEGF, KDR (kinase insert domain receptor), and hepatocyte growth factor (HGF). Rats transplanted with islets cocultured with preconditioned hASCs exhibited a better glycemic control than rats transplanted with an equal volume of islets and control hASCs. Cotransplantation with preconditioned hASCs was also associated with enhanced islet revascularization in vivo, as highlighted by graft morphological analysis. The observed increase in islet graft revascularization and function suggests that our method of stem cell preconditioning may represent a novel strategy to remarkably improve the efficacy of islets-hMSCs cotransplantation.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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