牛垂体结节部的66-kDa蛋白诱导大鼠远端部释放黄体生成素。

M. Lafarque, L. Oliveros
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引用次数: 1

摘要

在这项研究中,证据表明牛垂体结节部分泌的一种因子刺激大鼠远端部细胞释放黄体生成素(LH)。在分散的大鼠远部细胞上进行30min的培养和灌注实验,检测牛结节部细胞分泌到培养基中的产物。从结节部总细胞群中提取的培养基,每管添加6 μ g,诱导远端部细胞释放更多的LH,但对促卵泡激素(FSH)的释放没有影响。在不连续Percoll梯度下分离大鼠结节部细胞后,只有50%和60% Percoll强度的培养液才能释放出大鼠远部细胞中的LH。因此,将强度为50%和60%的Percoll细胞组分一起培养。为了获得最大的LH释放量(6倍于基础输出量),需要添加2毫克的结节部蛋白,这表明这些细胞产生影响远部促性腺激素细胞的因子。在12% SDS-PAGE上涂布结核菌培养基后,具有生物活性的条带为66-kDal。其洗脱物的50 ng蛋白释放的LH几乎是远部细胞基础输出量的9倍。结果表明,牛结节部蛋白对培养的大鼠远部促性腺激素细胞有调节作用。
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A 66-kDa protein of bovine hypophyseal Pars tuberalis induces luteinizing hormone release from rat Pars distalis.
In this study, evidence for a factor secreted by bovine hypophyseal pars tuberalis that stimulates luteinizing hormone (LH) release from rat pars distalis cells is shown. The secretion products of bovine pars tuberalis cells into the culture medium were assayed on dispersed rat pars distalis cells in 30 min incubations and superfusion experiments. The culture medium from pars tuberalis total cell populations, added at a dose of 6 microg per tube, induced the greater LH release from pars distalis cells, without effect on follicle stimulating hormone (FSH) release. After pars tuberalis cells separation on a discontinuos Percoll gradient, only the culture medium of cells from 50 and 60% strength Percoll were able to release LH from rat pars distalis cells. Therefore, cell fractions from 50 and 60% strenght Percoll were cultured together. To elicit maximal LH release (6 times the basal output), with the addition of 2 microg of pars tuberalis protein was required, suggesting that these cells produce the factor or factors which affect pars distalis gonadotrope cells. After applying the pars tuberalis culture medium on 12% SDS-PAGE, the band with biological activity was that of 66-kDal. Fifty ng protein of its eluate released almost 9 times the basal output of LH from pars distalis cells. Results suggest a modulating effect of a protein from the bovine pars tuberalis on rat cultured gonadotrope cells from the pars distalis.
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