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RFX6 Maintains Gene Expression and Function of Adult Human Islet α-Cells.
Coykendall, Vy M N; Qian, Mollie F; Tellez, Krissie; Bautista, Austin; Bevacqua, Romina J; Gu, Xueying; Hang, Yan; Neukam, Martin; Zhao, Weichen; Chang, Charles; MacDonald, Patrick E; Kim, Seung K.
Afiliación
  • Coykendall VMN; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA.
  • Qian MF; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA.
  • Tellez K; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA.
  • Bautista A; Department of Pharmacology and Alberta Diabetes Institute, University of Alberta, Edmonton, Alberta, Canada.
  • Bevacqua RJ; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA.
  • Gu X; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA.
  • Hang Y; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA.
  • Neukam M; Stanford Diabetes Research Center, Stanford University School of Medicine, Stanford, CA.
  • Zhao W; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA.
  • Chang C; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA.
  • MacDonald PE; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA.
  • Kim SK; Department of Pharmacology and Alberta Diabetes Institute, University of Alberta, Edmonton, Alberta, Canada.
Diabetes ; 73(3): 448-460, 2024 Mar 01.
Article en En | MEDLINE | ID: mdl-38064570
ABSTRACT
Mutations in the gene encoding the transcription factor regulatory factor X-box binding 6 (RFX6) are associated with human diabetes. 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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Islotes Pancreáticos / Diabetes Mellitus Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Islotes Pancreáticos / Diabetes Mellitus Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article