RFX6 maintains gene expression and function of adult human islet α cells

Author:

Coykendall Vy M. N.1,Qian Mollie F.1,Tellez Krissie1,Bautista Austin2,Bevacqua Romina J.1,Gu Xueying1,Hang Yan13,Neukam Martin1,Zhao Weichen1,Chang Charles1,MacDonald Patrick E.2,Kim Seung K.1453

Affiliation:

1. 1Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA

2. 2Department of Pharmacology and Alberta Diabetes Institute, University of Alberta, Edmonton, AB, Canada

3. 5Stanford Diabetes Research Center, Stanford University School of Medicine, Stanford, CA

4. 3Department of Medicine, Stanford University School of Medicine, Stanford, CA

5. 4Department of Pediatrics, Stanford University School of Medicine, Stanford, CA

Abstract

Mutations in the gene encoding the transcription factor RFX6 are associated with human diabetes mellitus. Within pancreatic islets, RFX6 expression is most abundant in islet α cells, and α cell RFX6 expression is altered in diabetes. However, the roles of RFX6 in regulating gene expression, glucagon output and other crucial human adult α cell functions are not yet understood. We developed a method for selective genetic targeting of human α cells and assessed RFX6-dependent α cell function. RFX6 suppression with RNA interference led to impaired α cell exocytosis and dysregulated glucagon secretion in vitro and in vivo. By contrast, these phenotypes were not observed with RFX6 suppression across all islet cells. Transcriptomics in α cells revealed RFX6-dependent expression of genes governing nutrient sensing, hormone processing, and secretion, with some of these exclusively expressed in human α cells. Mapping of RFX6 DNA-binding sites in primary human islet cells identified a subset of direct RFX6 target genes. Together, these data unveil RFX6-dependent genetic targets and mechanisms crucial for regulating adult human α cell function.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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