Sato N, Greer M A, Shimomura Y, Shimizu H, Uehara Y, Takahashi M, Ohshima K, Kobayashi I, Mori M
First Department of Internal Medicine, Gunma University.
Nihon Naibunpi Gakkai Zasshi. 1992 May 20;68(5):568-75. doi: 10.1507/endocrine1927.68.5_568.
It is still unknown how extracellular hyperosmolarity suppresses exocytosis. To evaluate the possibility that extracellular hyperosmolarity affects one of the most important second messenger system, Ca2+ signal, we evaluated the effect of hyperosmolarity on the thyrotropin releasing hormone (TRH)-induced changes in both intracellular Ca2+ concentration ([Ca2+]i) and prolactin (PRL) secretion in GH4C1 cells. TRH caused two phases of [Ca2+]i: an initial high-amplitude phase (first phase), which was not inhibited by Ca2+ free medium, and a sustained low-amplitude phase (second phase), which was abolished by Ca2+ free medium. Medium hyperosmolarity (isotonic = 300mOsm, hypertonic = 338, 375, 450, and 600mOsm) suppressed both TRH-induced phases of [Ca2+]i in a dose dependent manner, however, the suppressive effect was clearly stronger in the second phase of [Ca2+]i than in the first phase of [Ca2+]i. Low doses of medium hyperosmolarity (338 and 375mOsm) suppressed PRL secretion, which was dependent on Ca2+ influx. However, high doses of medium hyperosmolarity (450 and 600mOsm) also blocked PRL secretion, which was dependent on Ca2+ mobilized from cytosolic Ca2+ pools. These data indicate that in GH4C1 cells medium hyperosmolarity may inhibit PRL secretion by both blocking Ca2+ influx and a mechanism unrelated to Ca2+.
细胞外高渗如何抑制胞吐作用尚不清楚。为了评估细胞外高渗是否影响最重要的第二信使系统之一——Ca2+信号,我们在GH4C1细胞中评估了高渗对促甲状腺激素释放激素(TRH)诱导的细胞内Ca2+浓度([Ca2+]i)变化和催乳素(PRL)分泌的影响。TRH引起[Ca2+]i的两个阶段:初始高振幅阶段(第一阶段),不受无钙培养基抑制;持续低振幅阶段(第二阶段),被无钙培养基消除。培养基高渗(等渗=300mOsm,高渗=338、375、450和600mOsm)以剂量依赖方式抑制TRH诱导的[Ca2+]i的两个阶段,然而,对[Ca2+]i第二阶段的抑制作用明显强于第一阶段。低剂量的培养基高渗(338和375mOsm)抑制PRL分泌,这依赖于Ca2+内流。然而,高剂量的培养基高渗(450和600mOsm)也阻断PRL分泌,这依赖于从胞质Ca2+库动员的Ca2+。这些数据表明,在GH4C1细胞中,培养基高渗可能通过阻断Ca2+内流和一种与Ca2+无关的机制来抑制PRL分泌。