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大鼠中,促黄体生成素急性刺激下的睾丸间质细胞蛋白质合成与类固醇生成。

Leydig cell protein synthesis and steroidogenesis in response to acute stimulation by luteinizing hormone in rats.

作者信息

Luo L, Chen H, Stocco D M, Zirkin B R

机构信息

Division of Reproductive Biology, Johns Hopkins University School of Hygiene and Public Health, Baltimore, Maryland 21205, USA.

出版信息

Biol Reprod. 1998 Aug;59(2):263-70. doi: 10.1095/biolreprod59.2.263.

Abstract

We examined the temporal relationship between protein synthesis and testosterone production by rat Leydig cells in primary culture. Leydig cells were isolated from adult control Sprague-Dawley rats and from rats that had received LH-suppressive testosterone and estradiol (TE) implants in vivo for 10 days. The cells were incubated for 1-4 h with [35S]methionine in the presence or absence of maximally stimulating ovine LH, and newly synthesized proteins were examined by two-dimensional PAGE autoradiography. Approximately 800-900 newly synthesized polypeptides were readily visible on all autoradiograms, most of which did not differ in the cells from intact control and TE-treated rats. Incubation of cells from the control and treated rats with maximally stimulating LH for 4 h in both cases resulted in significant increases in testosterone production and in three newly synthesized polypeptides. These polypeptides, along with two others that changed little in response to LH, were similar in apparent molecular mass, 30 kDa, but differed in isoelectric point. Time-course studies revealed a temporal relationship between stimulation of the three 30-kDa proteins and of testosterone production. Western blot analysis identified the 30-kDa proteins as steroidogenic acute regulatory protein (StAR). The results of these studies, for the first time utilizing primary cultures of highly purified, testosterone-producing Leydig cells, provide further correlative evidence of a role for StAR protein in the acute regulation of Leydig cell testosterone biosynthesis by LH.

摘要

我们研究了原代培养的大鼠睾丸间质细胞中蛋白质合成与睾酮生成之间的时间关系。从成年对照斯普拉格 - 道利大鼠以及体内接受促黄体生成素(LH)抑制性睾酮和雌二醇(TE)植入物10天的大鼠中分离出睾丸间质细胞。在存在或不存在最大刺激量的绵羊LH的情况下,将细胞与[35S]甲硫氨酸一起孵育1 - 4小时,并通过二维聚丙烯酰胺凝胶电泳放射自显影法检测新合成的蛋白质。在所有放射自显影片上都能轻易看到大约800 - 900种新合成的多肽,其中大多数在完整对照大鼠和TE处理大鼠的细胞中没有差异。在两种情况下,将对照大鼠和处理大鼠的细胞与最大刺激量的LH一起孵育4小时,都会导致睾酮生成以及三种新合成多肽显著增加。这些多肽,连同另外两种对LH反应变化不大的多肽,表观分子量均为30 kDa,但等电点不同。时间进程研究揭示了三种30 kDa蛋白质的刺激与睾酮生成之间的时间关系。蛋白质印迹分析确定这三种30 kDa蛋白质为类固醇生成急性调节蛋白(StAR)。这些研究结果首次利用高度纯化的、产生睾酮的睾丸间质细胞原代培养物,进一步提供了相关证据,证明StAR蛋白在LH对睾丸间质细胞睾酮生物合成的急性调节中发挥作用。

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