支持细胞分泌蛋白刺激间质细胞睾酮产生的部分特征。

T Murai, K Noguchi, A Nagamoto, M Hosaka
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引用次数: 4

摘要

为了检验培养的未成熟大鼠Sertoli细胞是否分泌一种刺激成熟小鼠间质细胞产生睾酮的因子,我们从3周龄的雄性大鼠中制备了富含Sertoli细胞的培养物,并添加了胰蛋白酶和胶原酶。以3-5 × 10(6)个细胞/ 35mm孔的初始密度涂覆支持细胞,在添加胰岛素(10微克/毫升)的3ml无血清培养基中培养。每隔3天收集一次的支持细胞培养基(SCCM)加入10周龄小鼠机械分离的Leydig细胞(10(6)个细胞加入1 ml含2%不含类固醇的FCS的MEM)中,在34℃下孵育3小时。经Amicon YM10膜浓缩15倍的SCCM对睾酮产生的刺激呈剂量依赖性,而当LH对间质细胞刺激最大时,对睾酮分泌没有影响。孔径为24 a的透析膜和分子量截止值为10 kDa的超滤膜均保留了间质细胞刺激活性。然而,在60℃下加热30分钟,活性降低,在37℃下与0.1%胰蛋白酶孵育1小时后,活性几乎消失。通过Con a -琼脂糖柱,这种活性没有保留,仅在突破部分中得到证实。HPLC凝胶过滤15倍浓度的SCCM制剂在TSK凝胶G3000SW上显示Leydig细胞刺激活性约为13 kDa。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A partial characterization of a Sertoli cell-secreted protein stimulating Leydig cell testosterone production.

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)

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