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共培养中的粗线期精母细胞可抑制大鼠支持细胞中抑制素βB亚基和抑制素B的合成,但不影响抑制素α亚基的合成。

Pachytene spermatocytes in co-culture inhibit rat Sertoli cell synthesis of inhibin beta B-subunit and inhibin B but not the inhibin alpha-subunit.

作者信息

Clifton R J, O'Donnell L, Robertson D M

机构信息

Department of Obstetrics and Gynecology, Monash University, Clayton 3168, Victoria, Australia.

出版信息

J Endocrinol. 2002 Mar;172(3):565-74. doi: 10.1677/joe.0.1720565.

Abstract

This study investigates the effects of spermatogenic germ cells on inhibin alpha-subunit and beta B-subunit expression, and inhibin alpha-subunit and inhibin B production by rat Sertoli cells in vitro. Sertoli cells isolated from 19-day-old rats were cultured for 48 h at 32 degrees C, in the presence or absence of FSH (2.3-2350 mIU/ml), and in the presence of pachytene spermatocytes, round spermatids or cytoplasts of elongated spermatids purified from adult rat testis by elutriation and density gradient separation. Sertoli cell secretion of inhibin alpha-subunit and inhibin B, as measured by immunoassay, was dose-dependently stimulated by FSH (maximal stimulation 13- and 2-fold, respectively). Round spermatids or cytoplasts co-cultured with Sertoli cells had no effect on basal or FSH-induced secretion of inhibin alpha-subunit or inhibin B. When Sertoli cells were co-cultured with pachytene spermatocytes, inhibin alpha-subunit secretion was unaltered, while inhibin B secretion was suppressed in a cell concentration-dependent manner to reach a maximal suppression of 45% compared with Sertoli cells alone (P<0.01). A similar suppression in inhibin B was still observed (64% of Sertoli cells alone) when the pachytene spermatocytes were separated from Sertoli cells by a 0.45 microm pore membrane barrier in bicameral chambers. Pachytene spermatocytes also suppressed FSH-induced inhibin B levels in Sertoli cell co-cultures and this suppression was attributed to a decrease in basal inhibin B production rather than a change in FSH responsiveness. Quantitation of Sertoli cell inhibin alpha- and beta B-subunit mRNA by quantitative (real-time) PCR demonstrated that pachytene spermatocytes did not alter Sertoli cell alpha-subunit mRNA expression, but significantly (P<0.01) suppressed basal and FSH-induced beta B-subunit mRNA expression to a similar degree to that seen with inhibin B protein levels. It is concluded that pachytene spermatocytes in vitro suppress Sertoli cell inhibin B secretion via factor-mediated suppression of inhibin beta B-subunit expression. These findings support the hypothesis that specific germ cell types can influence inhibin B secretion by the testis independent of FSH regulation.

摘要

本研究调查了生精生殖细胞对大鼠支持细胞抑制素α亚基和βB亚基表达以及抑制素α亚基和抑制素B产生的影响。从19日龄大鼠分离的支持细胞在32℃下培养48小时,分别在有或无促卵泡激素(FSH,2.3 - 2350 mIU/ml)存在的情况下,以及在存在通过淘洗和密度梯度分离从成年大鼠睾丸纯化的粗线期精母细胞、圆形精子细胞或延长型精子细胞的胞质体的情况下进行培养。通过免疫测定法测量,支持细胞分泌抑制素α亚基和抑制素B受到FSH的剂量依赖性刺激(最大刺激分别为13倍和2倍)。与支持细胞共培养的圆形精子细胞或胞质体对抑制素α亚基或抑制素B的基础分泌或FSH诱导的分泌没有影响。当支持细胞与粗线期精母细胞共培养时,抑制素α亚基分泌未改变,而抑制素B分泌以细胞浓度依赖性方式受到抑制,与单独培养的支持细胞相比,最大抑制率达到45%(P<0.01)。当在双室培养箱中通过0.45微米孔径的膜屏障将粗线期精母细胞与支持细胞分离时,仍观察到抑制素B有类似程度的抑制(为单独培养的支持细胞的64%)。粗线期精母细胞还抑制了支持细胞共培养物中FSH诱导的抑制素B水平,这种抑制归因于基础抑制素B产生的减少,而不是FSH反应性的改变。通过定量(实时)PCR对支持细胞抑制素α和βB亚基mRNA进行定量分析表明,粗线期精母细胞未改变支持细胞α亚基mRNA表达,但显著(P<0.01)抑制基础和FSH诱导的βB亚基mRNA表达,抑制程度与抑制素B蛋白水平相似。结论是,体外培养的粗线期精母细胞通过因子介导的抑制素βB亚基表达抑制作用来抑制支持细胞抑制素B的分泌。这些发现支持了特定类型的生殖细胞可独立于FSH调节影响睾丸抑制素B分泌的假说。

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