BMP-7 Induces Adult Human Pancreatic Exocrine-to-Endocrine Conversion

Author:

Klein Dagmar1,Álvarez-Cubela Silvia1,Lanzoni Giacomo1,Vargas Nancy1,Prabakar Kamalaveni R.1,Boulina Maria1,Ricordi Camillo1234,Inverardi Luca135,Pastori Ricardo L.135,Domínguez-Bendala Juan126

Affiliation:

1. Diabetes Research Institute, Miller School of Medicine, University of Miami, Miami, FL

2. Department of Surgery, Miller School of Medicine, University of Miami, Miami, FL

3. Department of Microbiology and Immunology, Miller School of Medicine, University of Miami, Miami, FL

4. Department of Biomedical Engineering, Miller School of Medicine, University of Miami, Miami, FL

5. Department of Medicine, Miller School of Medicine, University of Miami, Miami, FL

6. Department of Cell Biology and Anatomy, Miller School of Medicine, University of Miami, Miami, FL

Abstract

The exocrine pancreas can give rise to endocrine insulin-producing cells upon ectopic expression of key transcription factors. However, the need for genetic manipulation remains a translational hurdle for diabetes therapy. Here we report the conversion of adult human nonendocrine pancreatic tissue into endocrine cell types by exposure to bone morphogenetic protein 7. The use of this U.S. Food and Drug Administration–approved agent, without any genetic manipulation, results in the neogenesis of clusters that exhibit high insulin content and glucose responsiveness both in vitro and in vivo. In vitro lineage tracing confirmed that BMP-7–induced insulin-expressing cells arise mainly from extrainsular PDX-1+, carbonic anhydrase II− (mature ductal), elastase 3a (acinar)−, and insulin− subpopulations. The nongenetic conversion of human pancreatic exocrine cells to endocrine cells is novel and represents a safer and simpler alternative to genetic reprogramming.

Funder

Diabetes Research Institute Foundation

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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