Transcriptional mechanisms of pancreatic 13-cell maturation and functional adaptation

被引:26
|
作者
Wortham, Matthew [1 ,2 ]
Sander, Maike [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Pediat, Pediat Diabet Res Ctr, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Cellular & Mol Med, Pediat Diabet Res Ctr, La Jolla, CA 92093 USA
来源
关键词
BETA-CELL MATURATION; INSULIN-SECRETION; GLUCOSE; GENE; MAFA; METABOLISM; TRIGGERS; IDENTITY; FOXA2; CARBOXYLASE;
D O I
10.1016/j.tem.2021.04.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pancreatic beta-cells secrete insulin commensurate to circulating nutrient levels to maintain normoglycemia. The ability of beta-cells to couple insulin secretion to nutrient stimuli is acquired during a postnatal maturation process. In mature beta-cells the insulin secretory response adapts to changes in nutrient state. Both beta-cell maturation and functional adaptation rely on the interplay between extracellular cues and cell type-specific transcriptional programs. Here we review emerging evidence that developmental and homeostatic regulation of beta-cell function involves collaboration between lineage-determining and signal-dependent transcription factors (LDTFs and SDTFs, respectively). A deeper understanding of beta-cell SDTFs and their cognate signals would delineate mechanisms of beta-cell maturation and functional adaptation, which has direct implications for diabetes therapies and for generating mature beta-cells from stem cells.
引用
收藏
页码:474 / 487
页数:14
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