ACCELERATION OF GROWTH OF CULTURED CARDIOMYOCYTES AND TRANSLOCATION ON OF PROTEIN-KINASE-C
ACCELERATION OF GROWTH OF CULTURED CARDIOMYOCYTES AND TRANSLOCATION ON OF PROTEIN-KINASE-C
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DOI:
10.1152/ajpcell.1992.263.2.c319
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发表时间:
1992-08-01
影响因子:
--
通讯作者:
MORGAN, HE
中科院分区:
文献类型:
--
作者:
ALLO, SN;CARL, LL;MORGAN, HE
Phorbol 12-myristate 13-acetate (PMA), norepinephrine (NE), and contraction stimulate cardiomyocyte growth (increased protein content). Differences exist in the time course and extent of protein and RNA accumulation. Cells plated at 4 x 10(6) cells/60-mm dish and arrested with 50 mM KCl demonstrated no significant growth. Treatment with PMA stimulated growth to a maximum of 17% at 48 h. In contrast, maximal stimulation of growth was 36 % at 48 h and 31 % at 72 h for contracting and NE-treated cells, respectively. Maximal stimulation of the capacity for protein synthesis (RNA content) was 32% for PMA-treated cells at 24 h compared with 59% and 77% for NE-treated and contracting cells, respectively, at 72 h. In support of a primary role for altered capacity in the regulation of protein synthesis, there was a significant correlation (r = 0.84) between RNA and protein contents that was independent of the stimulus used. Angiotensin II increased RNA content by 28% at 48 h but had no effect on growth up to 72 h. Growth stimulation and increased nuclear protein kinase C (PKC) activity were induced by contraction, NE, and PMA treatment and were inhibited by staurosporine (a PKC inhibitor), suggestive of a central role for PKC.