Concise Review: In Search of Unlimited Sources of Functional Human Pancreatic Beta Cells

Author:

Scharfmann Raphael1,Rachdi Latif1,Ravassard Philippe2

Affiliation:

1. Institut National de la Santé et de la Recherche Médicale U845 (INSERM U845), Research Center Growth and Signalling, Paris Descartes University, Sorbonne Paris Cité, Necker Hospital, Paris, France

2. Université Pierre et Marie Curie-Paris 6, Biotechnology and Biotherapy Team, Centre de Recherche de l'Institut du Cerveau et de la Moelle Épinière, Unité Mixte de Recherche Scientifique 975 (UMRS 975), Paris, France

Abstract

Abstract It is well-established that insulin-producing pancreatic beta cells are central in diabetes. In type 1 diabetes, beta cells are destroyed by an autoimmune mechanism, whereas in type 2 diabetes, there is a decrease in functional beta-cell mass. In this context, studying beta cells is of major importance. Beta cells represent only 1% of total pancreatic cells and are found dispersed in the pancreatic gland. During the past decades, many tools and approaches have been developed to study rodent beta cells that efficiently pushed the field forward. However, rodent and human beta cells are not identical, and our knowledge of human beta cells has not progressed as quickly as our understanding of rodent beta cells. We believe that one of the reasons for this inefficient progress is the difficulty of accessing unlimited sources of functional human pancreatic beta cells. The main focus of this review concerns recent strategies to generate new sources of human pancreatic beta cells.

Funder

seventh Framework Program

Innovative Medicines Initiative Joint Undertaking

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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