Julie P Mary, Arunakaran J, Malini T, Balasubramanian K
Department of Endocrinology, Dr. ALM Post Graduate Institute of Basic Medical Sciences, University of Madras, Chennai, Tamil Nadu, India.
Endocr Res. 2003 Aug;29(3):327-41. doi: 10.1081/erc-120025040.
The role of luteinizing hormone (LH), prolactin and their combination in the regulation of insulin receptors in Leydig cells was studied. Leydig cells were isolated from adult male Wistar rats and measurement of insulin binding and internalization was done by incubating the cells with a saturating concentration of 125I-insulin in the presence or absence of different doses of unlabeled LH/insulin. LH exposure (100 and 200 ng dose) caused a significant increase in Leydig cell surface and internalized insulin receptor concentrations. Prolactin at all doses was ineffective in inducing a significant change in insulin receptor concentration. Under basal condition, Leydig cell surface binding of 125I-insulin was greater than the internalization at 34 degrees C but at 4 degrees C, surface binding remained lower than that at 34 degrees C with negligible internalization. Internalization of insulin receptors was measured by incubating the cells at 4 degrees C for 16h and then rapidly incubating at 34 degrees C for various time intervals (60, 120, and 180 min). LH/PRL or LH + PRL did not induce any significant change in the internalization of 125I-insulin at 60 and 120 min. The rate of internalization was greater at 120 min in basal as well as LH/PRL exposed Leydig cells, compared to 60 min of incubation. Prolactin alone did not evoke any appreciable change in internalization of 125I-insulin compared to basal at all three time points tested. Total and acid soluble release of 125I-insulin recorded a significant increase in Leydig cells exposed to LH, which was marginally potentiated when prolactin was added along with LH. Monensin treatment of Leydig cells prevented the recycling of insulin receptors to the cell surface and thereby suppressed the surface binding and enhanced the internalized 125I-insulin. Under cycloheximide treatment, neither surface bound nor internalized 125I-insulin recorded a significant change compared to their respective basal values. It is concluded from the present study that LH has dose-dependent biphasic effects on insulin receptors in Leydig cells by modulating the internalization and intracellular processing of hormone-receptor complexes but prolactin has no such effects.
研究了促黄体生成素(LH)、催乳素及其组合在调节睾丸间质细胞胰岛素受体中的作用。从成年雄性Wistar大鼠中分离出睾丸间质细胞,通过在存在或不存在不同剂量未标记的LH/胰岛素的情况下,用饱和浓度的125I-胰岛素孵育细胞来测量胰岛素结合和内化情况。暴露于LH(100和200 ng剂量)导致睾丸间质细胞表面和内化胰岛素受体浓度显著增加。所有剂量的催乳素在诱导胰岛素受体浓度显著变化方面均无效。在基础条件下,34℃时睾丸间质细胞对125I-胰岛素的表面结合大于内化,但在4℃时,表面结合仍低于34℃时,内化可忽略不计。通过在4℃孵育细胞16小时,然后在34℃快速孵育不同时间间隔(60、120和180分钟)来测量胰岛素受体的内化。在60和120分钟时,LH/PRL或LH + PRL对125I-胰岛素的内化未诱导任何显著变化。与孵育60分钟相比,在基础以及暴露于LH/PRL的睾丸间质细胞中,120分钟时的内化速率更高。在所有三个测试时间点,单独的催乳素与基础相比,在125I-胰岛素内化方面未引起任何明显变化。暴露于LH的睾丸间质细胞中,125I-胰岛素的总释放和酸溶性释放显著增加,当与LH一起添加催乳素时略有增强。莫能菌素处理睾丸间质细胞可阻止胰岛素受体循环至细胞表面,从而抑制表面结合并增强内化的125I-胰岛素。在环己酰亚胺处理下,与各自的基础值相比,表面结合和内化的125I-胰岛素均未记录到显著变化。本研究得出结论,LH通过调节激素-受体复合物的内化和细胞内加工,对睾丸间质细胞中的胰岛素受体具有剂量依赖性双相作用,但催乳素没有这种作用。