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PDX-1 and MafA Play a Crucial Role in Pancreatic β-Cell Differentiation and Maintenance of Mature β-Cell Function

机译:PDX-1和MafA在胰腺β细胞分化和维持成熟β细胞功能中起关键作用

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摘要

Pancreatic and duodenal homeobox factor-1 (PDX-1) plays a crucial role in pancreas development, β-cell differentiation, and maintenance of mature β-cell function. PDX-1 expression is maintained in pancreatic precursor cells during pancreas development but becomes restricted to β-cells in mature pancreas. In mature (β-cells, PDX-1 transactivates the insulin and other genes involved in glucose sensing and metabolism such as GLUT2 and glucokinase. MafA is a recently isolated β-cell-specific transcription factor which functions as a potent activator of insulin gene transcription. Furthermore, these transcription factors play an important role in induction of insulin-producing cells in various non-β-cells and thus could be therapeutic targets for diabetes. On the other hand, under diabetic conditions, expression and/or activities of PDX-1 and MafA in β-cells are reduced, which leads to suppression of insulin biosynthesis and secretion. It is likely that alteration of such transcription factors explains, at least in part, the molecular mechanism for β-cell glucose toxicity found in diabetes.
机译:胰腺和十二指肠同源盒因子1(PDX-1)在胰腺发育,β细胞分化和维持成熟的β细胞功能中起着至关重要的作用。在胰腺发育过程中,PDX-1的表达在胰腺前体细胞中得以维持,但在成熟的胰腺中却仅限于β细胞。在成熟的(β细胞)中,PDX-1激活胰岛素和其他参与葡萄糖感测和代谢的基因,例如GLUT2和葡萄糖激酶。MafA是最近分离出的β细胞特异性转录因子,可作为胰岛素基因转录的有效激活剂。此外,这些转录因子在各种非β细胞的胰岛素产生细胞的诱导中起着重要作用,因此可能成为糖尿病的治疗靶标;另一方面,在糖尿病条件下,PDX-的表达和/或活性β和MafA在β细胞中的减少,导致胰岛素生物合成和分泌的抑制,这种转录因子的改变可能至少部分地解释了糖尿病中β细胞葡萄糖毒性的分子机制。

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