REGULATION OF GENE-TRANSCRIPTION AND PROLIFERATION BY PARATHYROID-HORMONE IS BLOCKED IN MUTANT OSTEOBLASTIC CELLS RESISTANT TO CYCLIC-AMP

被引:8
|
作者
ZAJAC, JD
KEARNS, AK
SKURAT, RM
KRONENBERG, HM
BRINGHURST, FR
机构
[1] MASSACHUSETTS GEN HOSP,ENDOCRINE UNIT,WELLMAN 5,BOSTON,MA 02114
[2] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02115
关键词
PARATHYROID HORMONE; CYCLIC AMP; OSTEOSARCOMA CELLS (RAT); SIGNAL TRANSDUCTION; PROLIFERATION; PROTEIN KINASE-A;
D O I
10.1016/0303-7207(92)90234-W
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We employed a cyclic AMP-resistant subclone of UMR 106-01 osteoblastic osteosarcoma cells (UMR 4-7) with a regulated, dominant-negative mutation of cyclic AMP-dependent protein kinase (PK-A), to examine the mechanism(s) whereby parathyroid hormone (PTH) regulates growth of these cells. Expression of a transiently transfected CAT reporter gene controlled by the cAMP response element of the rat somatostatin gene ('SST-CAT') was used to monitor PK-A activation in intact cells. Agonist-stimulated SST-CAT expression was specific for agents known to activate adenylate cyclase, required an intact cAMP response element and was specifically blocked following induction of the mutant cAMP-resistant phenotype in UMR 4-7 cells. Inhibition of the proliferation of UMR 106-01 cells by PTH, which is mimicked by forskolin and 8-bromo-cAMP, was blocked completely in mutant cyclic AMP-resistant UMR 4-7 cells. We conclude that control of proliferation in UMR 106-01 cells by PTH involves the cAMP messenger system and requires activation of PK-A.
引用
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页码:69 / 77
页数:9
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