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激活素、抑制素和卵泡抑素变体在成年雄性小鼠生殖道中的表达模式表明它们在附睾和输精管中发挥重要作用。

Expression patterns of activin, inhibin and follistatin variants in the adult male mouse reproductive tract suggest important roles in the epididymis and vas deferens.

作者信息

Winnall Wendy R, Wu Hui, Sarraj Mai A, Rogers Peter A W, de Kretser David M, Girling Jane E, Hedger Mark P

机构信息

Centre for Reproduction and Development, Monash Institute of Medical Research, Monash University, Clayton, Vic. 3168, Australia.

出版信息

Reprod Fertil Dev. 2013;25(3):570-80. doi: 10.1071/RD11287.

Abstract

Activin A and its inhibitors follistatin and inhibin play key roles in development and function of the male reproductive tract. Quantitative (q) polymerase chain reaction (PCR) was used to evaluate the expression of Inhba (the gene encoding activin A subunits), Inha and Inhbb (genes encoding the inhibin B subunits), as well as the genes for follistatin (Fst) and follistatin-like 3 (Fstl3) and the activin receptor subunits, in the male mouse reproductive tract. A qPCR assay that discriminated between the two follistatin variants of Fst288 (tissue-bound form) and Fst315 (circulating) was established. Activin A protein was measured by ELISA, whereas the inhibin α-subunit and total follistatin proteins were measured by radioimmunoassay (RIA). A screen of 22 tissues demonstrated tissue-specific regulation of the follistatin variants, with Fst288 highly expressed in the vas deferens and Fst315 most highly expressed in the skin. The expression of Fst288 and Fst315 and follistatin protein levels increased progressively from the testis through to the distal vas deferens. Inhba and the activin receptors were highly expressed in the epididymis, but activin A protein was elevated in both the epididymis and vas deferens. Inhibin α-subunit mRNA and protein and Inhbb expression were highest in the testis. These results indicate a role for activin A within the epididymis, but also that activin A bioactivity may be increasingly inhibited by follistatin distally along the male reproductive tract.

摘要

激活素A及其抑制剂卵泡抑素和抑制素在雄性生殖道的发育和功能中发挥关键作用。采用定量(q)聚合酶链反应(PCR)评估抑制素βA(编码激活素A亚基的基因)、抑制素α和抑制素βB(编码抑制素B亚基的基因)以及卵泡抑素(Fst)、卵泡抑素样3(Fstl3)和激活素受体亚基的基因在雄性小鼠生殖道中的表达。建立了一种qPCR检测方法,可区分Fst288(组织结合形式)和Fst315(循环形式)这两种卵泡抑素变体。通过酶联免疫吸附测定(ELISA)检测激活素A蛋白,而通过放射免疫测定(RIA)检测抑制素α亚基和总卵泡抑素蛋白。对22种组织的筛查显示了卵泡抑素变体的组织特异性调控,Fst288在输精管中高表达,Fst315在皮肤中表达最高。从睾丸到输精管远端,Fst288和Fst315的表达以及卵泡抑素蛋白水平逐渐升高。抑制素βA和激活素受体在附睾中高表达,但激活素A蛋白在附睾和输精管中均升高。抑制素α亚基mRNA和蛋白以及抑制素βB的表达在睾丸中最高。这些结果表明激活素A在附睾中发挥作用,但也表明沿着雄性生殖道远端,激活素A的生物活性可能越来越受到卵泡抑素的抑制。

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