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一种刺激睾丸间质细胞睾酮生成的支持细胞分泌蛋白的部分特性

A partial characterization of a Sertoli cell-secreted protein stimulating Leydig cell testosterone production.

作者信息

Murai T, Noguchi K, Nagamoto A, Hosaka M

机构信息

Department of Urology, Yokohama City University, School of Medicine, Japan.

出版信息

Endocrinol Jpn. 1992 Apr;39(2):209-15. doi: 10.1507/endocrj1954.39.209.

DOI:10.1507/endocrj1954.39.209
PMID:1396352
Abstract

To examine whether immature rat Sertoli cells in culture secrete a factor(s) which stimulates testosterone production by mature mouse Leydig cells, Sertoli cell-enriched cultures were prepared from 3-week-old male rats with trypsin and collagenase. Sertoli cells were plated at an initial density of 3-5 x 10(6) cells/35 mm well and cultured in 3 ml serum free media supplemented with insulin (10 micrograms/ml). Sertoli cell culture medium (SCCM) collected every 3rd day was added to Leydig cells (10(6) cells in 1 ml of MEM with 2% steroid-free FCS) prepared from 10-week-old mice by mechanical separation and incubated for 3 h at 34 degrees C. Secreted testosterone was determined by RIA. SCCM 15 times concentrated by Amicon YM10 membrane demonstrated a dose-dependent stimulation of testosterone production, whereas there was no effect on testosterone secretion when Leydig cells were maximally stimulated by LH. Leydig cell stimulating activity was retained by both a dialysis membrane with a pore size of 24 A and an ultrafiltration membrane with a molecular weight cut-off of 10 kDa. However, activity was reduced by heating at 60 degrees C for 30 min and almost lost after incubation with 0.1% trypsin for 1 h at 37 degrees C. This activity was not retained by means of a Con A-Agarose column and was demonstrated only in break-through fractions. HPLC gel filtration of a 15 times concentrated SCCM preparation on a TSK gel G3000SW revealed Leydig cell-stimulating activity at approximately 13 kDa.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了检测培养的未成熟大鼠支持细胞是否分泌刺激成熟小鼠睾丸间质细胞产生睾酮的因子,用胰蛋白酶和胶原酶从3周龄雄性大鼠制备富含支持细胞的培养物。支持细胞以3 - 5×10(6)个细胞/35 mm孔的初始密度接种,在补充有胰岛素(10微克/毫升)的3毫升无血清培养基中培养。每3天收集的支持细胞培养基(SCCM)加入到通过机械分离从10周龄小鼠制备的睾丸间质细胞(10(6)个细胞于1毫升含2%无类固醇胎牛血清的MEM中)中,在34℃孵育3小时。通过放射免疫分析法测定分泌的睾酮。经Amicon YM10膜浓缩15倍的SCCM显示出对睾酮产生的剂量依赖性刺激,而当用促黄体生成素(LH)最大程度刺激睾丸间质细胞时,对睾酮分泌没有影响。孔径为24 Å的透析膜和截留分子量为10 kDa的超滤膜都保留了睾丸间质细胞刺激活性。然而,在60℃加热30分钟活性降低,在37℃与0.1%胰蛋白酶孵育1小时后几乎丧失。这种活性不能通过伴刀豆球蛋白A -琼脂糖柱保留,仅在穿透组分中显示。在TSK凝胶G3000SW上对15倍浓缩的SCCM制剂进行高效液相色谱凝胶过滤,显示在约13 kDa处有睾丸间质细胞刺激活性。(摘要截短于250字)

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