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一些促细胞分裂剂会使成纤维细胞中的游离钙迅速增加。

Some mitogens cause rapid increases in free calcium in fibroblasts.

作者信息

Morris J D, Metcalfe J C, Smith G A, Hesketh T R, Taylor M V

出版信息

FEBS Lett. 1984 Apr 24;169(2):189-93. doi: 10.1016/0014-5793(84)80316-6.

Abstract

Quiescent 3T3 fibroblasts grown on microcarrier beads and loaded with the [Ca2+] indicator quin2 had a cytosolic free Ca2+ concentration ( [Ca2+]i) of 154 +/- 11 nM (SE; n = 32). Stimulation with the mitogens vasopressin, epidermal growth factor (EGF) or prostaglandin F2 alpha (PGF2 alpha) caused a very rapid increase in [Ca2+]i to a maximum of 200-500 nM after 60-90 s. [Ca2+]i declined thereafter to a level above that in quiescent cells which was maintained for at least 15 min. In contrast no immediate effects on [Ca2+]i were detected after the addition of the mitogens insulin or 12-O-tetradecanoylphorbol 13-acetate (TPA). These studies indicate that early changes in [Ca2+]i may be involved in the action on fibroblasts of some, but not all, mitogens.

摘要

生长在微载体珠上并负载有[Ca2+]指示剂喹啉-2的静止3T3成纤维细胞,其胞质游离Ca2+浓度([Ca2+]i)为154±11 nM(标准误;n = 32)。用促有丝分裂原血管加压素、表皮生长因子(EGF)或前列腺素F2α(PGF2α)刺激后,[Ca2+]i在60 - 90秒内迅速升高至最大值200 - 500 nM。此后,[Ca2+]i下降至高于静止细胞的水平,并维持至少15分钟。相比之下,添加促有丝分裂原胰岛素或12 - O - 十四烷酰佛波醇13 - 乙酸酯(TPA)后,未检测到对[Ca2+]i有即时影响。这些研究表明,[Ca2+]i的早期变化可能参与了某些(但不是所有)促有丝分裂原对成纤维细胞的作用。

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