Paired box 6 gene delivery preserves beta cells and improves islet transplantation efficacy

Author:

So Wing Yan1ORCID,Liao Yilie123,Liu Wai Nam1,Rutter Guy A456,Han Weiping1ORCID

Affiliation:

1. Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR) Singapore Singapore

2. Zhongshan Institute for Drug Discovery Shanghai Institute of Materia Medica Chinese Academy of Sciences Zhongshan Guangdong 528400 China

3. Center for Neurometabolism and Regenerative Medicine Bioland Laboratories Guangzhou Guangdong 510530 China

4. Centre de Recherche du CHUM, Faculté de Médicine Université de Montréal Montréal QC Canada

5. Section of Cell Biology and Functional Genomics, Division of Diabetes, Endocrinology and Metabolism, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine Imperial College London London UK

6. Lee Kong Chian Imperial Medical School Nanyang Technological University Singapore Singapore

Abstract

AbstractLoss of pancreatic beta cells is the central feature of all forms of diabetes. Current therapies fail to halt the declined beta cell mass. Thus, strategies to preserve beta cells are imperatively needed. In this study, we identified paired box 6 (PAX6) as a critical regulator of beta cell survival. Under diabetic conditions, the human beta cell line EndoC‐βH1, db/db mouse and human islets displayed dampened insulin and incretin signalings and reduced beta cell survival, which were alleviated by PAX6 overexpression. Adeno‐associated virus (AAV)‐mediated PAX6 overexpression in beta cells of streptozotocin‐induced diabetic mice and db/db mice led to a sustained maintenance of glucose homeostasis. AAV‐PAX6 transduction in human islets reduced islet graft loss and improved glycemic control after transplantation into immunodeficient diabetic mice. Our study highlights a previously unappreciated role for PAX6 in beta cell survival and raises the possibility that ex vivo PAX6 gene transfer into islets prior to transplantation might enhance islet graft function and transplantation outcome.

Funder

Diabetes UK

Wellcome Trust

Agency for Science, Technology and Research

Biomedical Research Council

Publisher

Springer Science and Business Media LLC

Subject

Molecular Medicine

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