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Stimulation of creatine kinase BB activity by parathyroid hormone and by prostaglandin E2 in cultured bone cells.

机译:甲状旁腺激素和前列腺素E2刺激培养的骨细胞中的肌酸激酶BB活性。

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摘要

Bone cells in culture responded to parathyroid hormone (PTH) and prostaglandin E2 (PGE2) by a 2-fold increase in creatine kinase (CK) activity. Combined treatment resulted in a higher response than with PTH alone. Calcitonin (CT) failed to stimulate CK activity, did not affect the response of CK to PTH, but inhibited slightly the increase in CK activity by PGE2. Bone-cell cultures grown in low [Ca2+] (0.125 mM), enriched in PTH-responsive osteoblast-like cells, responded to PTH, but not to PGE2 or CT, by increased CK activity. In both normal and low-[Ca2+] cultures, 8-bromo cyclic AMP did not affect CK activity, nor did it change the response of the cells to PTH, PGE2 or CT. The increase in CK activity was time- and dose-dependent and inhibited both by cycloheximide and by actinomycin D. The isoenzyme of CK stimulated was the CKBB form, the isoenzyme induced by other hormones. This appears to be the first report of the stimulation of CK activity by a polypeptide hormone or a prostaglandin. We suggest that stimulation of CKBB can serve as a marker for the action of a variety of hormones and growth promoters.
机译:培养中的骨细胞对甲状旁腺激素(PTH)和前列腺素E2(PGE2)的反应是肌酸激酶(CK)活性增加了2倍。联合治疗比单独使用PTH产生更高的反应。降钙素(CT)不能刺激CK的活性,不影响CK对PTH的反应,但会稍微抑制PGE2引起的CK活性的增加。在低[Ca2 +](0.125 mM)下生长,富含PTH反应性成骨细胞样细胞的骨细胞培养物通过增加CK活性而对PTH反应,但对PGE2或CT反应不大。在正常和低[Ca2 +]培养中,8溴环AMP均不会影响CK活性,也不会改变细胞对PTH,PGE2或CT的反应。 CK活性的增加是时间和剂量依赖性的,并被环己酰亚胺和放线菌素D抑制。刺激的CK同工酶是CKBB形式,其他激素诱导的同工酶。这似乎是多肽激素或前列腺素刺激CK活性的首次报道。我们建议对CKBB的刺激可以作为多种激素和生长促进剂作用的标志。

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