The differential regulation of steroidogenic acute regulatory protein-mediated steroidogenesis by type I and type II PKA in MA-10 cells

被引:46
作者
Dyson, Matthew T. [1 ]
Kowalewski, Mariusz P. [1 ]
Manna, Pulak R. [1 ]
Stocco, Douglas M. [1 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Dept Biochem & Cell Biol, Lubbock, TX 79430 USA
关键词
Steroidogenesis; STAR; CAMP-dependent protein kinase; PKA; CAM P; Leydig; HORMONE-SENSITIVE LIPASE; STAR MESSENGER-RNA; KINASE TYPE-I; HUMAN CHORIONIC-GONADOTROPIN; ELEMENT BINDING-PROTEIN; LEYDIG TUMOR-CELLS; CYCLIC-AMP; GENE-EXPRESSION; LUTEINIZING-HORMONE; MITOCHONDRIAL PROTEIN;
D O I
10.1016/j.mce.2008.11.029
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Following tropic hormone challenge, steroidogenic tissues utilize PKA to phosphorylate unique subsets of proteins necessary to facilitate steroidogenesis. This includes the PKA-dependent expression and activation of the steroidogenic acute regulatory protein (STAR), which mediates the rate-limiting step of steroidogenesis by inducing the transfer of cholesterol from the outer to the inner mitochondrial membrane. Since both type I and type II PKA are present in steroidogenic tissues, we have utilized CAMP analog pairs that preferentially activate each PKA subtype in order to examine their impact on STAR synthesis and activity. In MA-10 mouse Leydig tumor cells Star gene expression is more dependent upon type 1 PKA, while the post-transcriptional regulation of STAR appears subject to type II PKA. These experiments delineate the discrete effects that type I and type 11 PKA exert on STAR-mediated steroidogenesis, and suggest complimentary roles for each subtype in coordinating steroidogenesis. Published by Elsevier Ireland Ltd.
引用
收藏
页码:94 / 103
页数:10
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