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生长抑素通过转录后机制抑制仓鼠胰岛细胞系中的胰岛素基因表达。

Somatostatin inhibits insulin-gene expression through a posttranscriptional mechanism in a hamster islet cell line.

作者信息

Philippe J

机构信息

Department of Genetics and Microbiology, Centre Médical Universitaire, Geneva, Switzerland.

出版信息

Diabetes. 1993 Feb;42(2):244-9. doi: 10.2337/diab.42.2.244.

Abstract

Insulin secretion is regulated by the interplay of nutrients, local intraislet factors, and hormones. Nutrients involved in the positive control of insulin secretion, such as glucose and amino acid, also act on insulin biosynthesis. SRIF is one of the most potent inhibitors of insulin secretion. To determine whether SRIF also regulates insulin biosynthesis, we studied its effects on insulin-gene expression. SRIF decreases steady-state insulin mRNA levels in a clonal hamster islet cell line, HIT-T15, in a dose- and time-dependent manner; this decrease does not occur at the transcriptional level but essentially at a posttranscriptional level. We conclude that SRIF not only modulates insulin secretion but also affects insulin-gene expression.

摘要

胰岛素分泌受营养物质、胰岛局部因子和激素之间相互作用的调节。参与胰岛素分泌正向调控的营养物质,如葡萄糖和氨基酸,也作用于胰岛素生物合成。生长抑素是胰岛素分泌最有效的抑制剂之一。为了确定生长抑素是否也调节胰岛素生物合成,我们研究了其对胰岛素基因表达的影响。生长抑素以剂量和时间依赖性方式降低克隆仓鼠胰岛细胞系HIT-T15中的稳态胰岛素mRNA水平;这种降低并非发生在转录水平,而是主要发生在转录后水平。我们得出结论,生长抑素不仅调节胰岛素分泌,还影响胰岛素基因表达。

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