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激活素抑制而抑制素激活小鼠胎盘催乳素-II的分泌。

Activin inhibits but inhibin activates mouse placental lactogen-II secretion.

作者信息

Yamaguchi M, Tasaka K, Ogura K, Sakata M, Mizuki J, Miyake A

机构信息

Department of Obstetrics and Gynecology, Osaka University Medical School, Japan.

出版信息

J Endocrinol. 1995 Sep;146(3):469-74. doi: 10.1677/joe.0.1460469.

Abstract

The regulation of mouse placental lactogen (mPL)-I and mPL-II secretion by activin and inhibin and the expression of activin and inhibin subunit mRNAs in the mouse decidua were examined. Activin-A at a concentration of 10 nM/l significantly inhibited mPL-II secretion by placental cells from days 9 and 12 of pregnancy. However, activin-A did not affect mPL-I secretion by cells from days 7 and 9 of pregnancy nor mPL-II secretion by cells from day 7 of pregnancy. By contrast, 10 nM/l inhibin activated mPL-II secretion by cells from day 12 of pregnancy. These effects of activin and inhibin on mPL-II secretion were dose-dependent. Follistatin, which binds to activin and blocks its bioactivity, completely eliminated the inhibitory effect of activin on mPL-II secretion. Incubation of placental cells from day 12 of pregnancy with activin-A resulted in a significant reduction of the mPL-II mRNA level assessed by Northern blot analysis. Northern blot analysis using poly(A)+RNA extracted from the decidua indicated that mouse decidua, as well as the placenta, express all activin and inhibin subunits and that their gene expressions increased during gestation. The expression of these mRNAs in the decidua was much higher than those in the placenta. These findings suggest that activin and inhibin regulate mPL-II secretion and suggest the presence of an autocrine or paracrine regulation of mPL-II secretion in mouse placenta by activin and inhibin after mid-pregnancy in vivo.

摘要

研究了激活素和抑制素对小鼠胎盘催乳素(mPL)-I和mPL-II分泌的调节作用以及激活素和抑制素亚基mRNA在小鼠蜕膜中的表达。浓度为10 nM/l的激活素-A可显著抑制妊娠第9天和第12天胎盘细胞分泌mPL-II。然而,激活素-A不影响妊娠第7天和第9天细胞分泌mPL-I,也不影响妊娠第7天细胞分泌mPL-II。相比之下,10 nM/l的抑制素可激活妊娠第12天细胞分泌mPL-II。激活素和抑制素对mPL-II分泌的这些作用呈剂量依赖性。与激活素结合并阻断其生物活性的卵泡抑素完全消除了激活素对mPL-II分泌的抑制作用。用激活素-A孵育妊娠第12天的胎盘细胞,通过Northern印迹分析评估,mPL-II mRNA水平显著降低。使用从蜕膜中提取的poly(A)+RNA进行的Northern印迹分析表明,小鼠蜕膜以及胎盘均表达所有激活素和抑制素亚基,且它们的基因表达在妊娠期增加。这些mRNA在蜕膜中的表达远高于在胎盘中的表达。这些发现表明激活素和抑制素调节mPL-II分泌,并提示在体内妊娠中期后,激活素和抑制素在小鼠胎盘中对mPL-II分泌存在自分泌或旁分泌调节。

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