Signal transduction via TRPM3 channels in pancreatic β-cells

被引:34
作者
Thiel, Gerald [1 ]
Mueller, Isabelle [1 ]
Roessler, Oliver G. [1 ]
机构
[1] Univ Saarland, Med Ctr, Dept Med Biochem & Mol Biol, D-66421 Homburg, Germany
关键词
Gene regulation; Pancreatic beta-cell; Signal transduction; Steroids; Calcium signaling; STEROID MODULATORY DOMAIN; PROTEIN-KINASE-C; PREGNENOLONE SULFATE; TRANSCRIPTION FACTORS; SYNAPTIC-TRANSMISSION; GENE-TRANSCRIPTION; INSULIN-SECRETION; GLUCOSE; ACTIVATION; EXPRESSION;
D O I
10.1530/JME-12-0237
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Transient receptor potential melastatin 3 (TRPM3) channels are non-selective cation channels that are expressed in insulinoma cells and pancreatic beta-cells. Stimulation of TRPM3 with the neurosteroid pregnenolone sulfate induces an intracellular signaling cascade, involving a rise in intracellular Ca2+ concentration, activation of the protein kinases Raf and ERK, and a change in the gene expression pattern of the cells. In particular, biosynthesis of insulin is altered following activation of TRPM3 by pregnenolone sulfate. Moreover, a direct effect of TRPM3 stimulation on insulin secretion has been reported. The fact that stimulation of TRPM3 induces a signaling cascade that is very similar to the signaling cascade induced by glucose in beta-cells suggests that TRPM3 may influence main functions of pancreatic beta-cells. The view that TRPM3 represents an ionotropic steroid receptor of pancreatic beta-cells linking insulin release with steroid hormone signaling is discussed.
引用
收藏
页码:R75 / R83
页数:9
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