Starzec A, Jutisz M, Counis R
Laboratoire des Hormones Polypeptidiques, Centre National de la Recherche Scientifique, Gif sur Yvette, France.
Biochem Biophys Res Commun. 1988 Jun 16;153(2):664-70. doi: 10.1016/s0006-291x(88)81146-x.
We have studied the time course (0-5h) of the stimulatory effect of the hypothalamic gonadotropin-releasing hormone (GnRH) on the biosynthesis of lutropin (LH) polypeptide chains, as measured by the incorporation of [35S] methionine into proteins synthesized in cultured rat anterior pituitary cells in the absence or presence of 10nM GnRH. Labeled polypeptides, immunologically related to LH subunits alpha and beta, were isolated by specific immunoprecipitation, analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, then revealed by fluorography and quantified by counting the excised bands. This methodology allowed us to detect the radioactivity incorporated into LH subunits after less than 15 min of incubation. During first 1h of the time-course the quantity of [35S]Met incorporated into both alpha and LH beta subunits was not increased by the presence of GnRH in the incubation medium. A significant increase in the incorporation of radioactivity into LH subunits was observed after 2h of GnRH treatment. However, the increase in LH release into the medium in response to GnRH, as measured by RIA, was immediate. These data demonstrate that GnRH-stimulated synthesis of LH polypeptide chains occurs after a lag of approximately 1h and involves mechanisms different from those governing the stimulation of LH release.
我们研究了下丘脑促性腺激素释放激素(GnRH)对促黄体生成素(LH)多肽链生物合成的刺激作用的时间进程(0 - 5小时),这是通过在不存在或存在10nM GnRH的情况下,将[35S]甲硫氨酸掺入培养的大鼠垂体前叶细胞中合成的蛋白质来测量的。通过特异性免疫沉淀分离出与LH亚基α和β免疫相关的标记多肽,通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳进行分析,然后通过荧光自显影显示,并通过对切下的条带进行计数来定量。这种方法使我们能够在孵育不到15分钟后检测到掺入LH亚基中的放射性。在时间进程的最初1小时内,孵育培养基中存在GnRH并不会增加掺入α和LHβ亚基中的[35S]甲硫氨酸的量。在GnRH处理2小时后,观察到掺入LH亚基中的放射性显著增加。然而,通过放射免疫分析(RIA)测量,GnRH刺激LH释放到培养基中的增加是即时的。这些数据表明,GnRH刺激的LH多肽链合成在大约1小时的延迟后发生,并且涉及与控制LH释放刺激的机制不同的机制。