首页> 外文期刊>Molecular reproduction and development >Effects of BMP4/SMAD signaling pathway on mouse primordial follicle growth and survival via up-regulation of Sohlh2 and c-kit
【24h】

Effects of BMP4/SMAD signaling pathway on mouse primordial follicle growth and survival via up-regulation of Sohlh2 and c-kit

机译:BMP4 / SMAD信号通路通过上调Sohlh2和c-kit对小鼠原始卵泡生长和存活的影响

获取原文
获取原文并翻译 | 示例
           

摘要

Bone morphogenetic protein 4 (BMP4) is essential for the development of primordial follicles, although its underlying mechanism remains largely unknown. By using cultured ovaries, the effects of BMP4 and the potential signal transduction pathways were investigated. Ovaries from 3-day-old female mouse pups were maintained in organ culture in the absence (control) or presence of BMP4 (100ng/ml). At different culture time, the effects of BMP4 on primordial follicle growth and survival were assayed by follicle count and TUNEL labeling. The expression of phospho-SMAD1/5/8, Sohlh2, and c-kit were measured by immunohistochemistry, RT-PCR, and Western blotting. Immunohistochemistry was also performed to determine the expression pattern of BMP4, pSMAD1/5/8, Sohlh2, and c-kit in vivo during ovarian development. The results showed treatments of ovaries with BMP4 resulted in a significant (P<0.05) increase on the primordial-to-primary follicle transition. The oocytes of primordial follicles treated with BMP4 were also less likely to undergo apoptosis. BMP4 enhanced the phosphorylation of SMAD1/5/8 and up-regulated the expression of Sohlh2 and c-kit in primordial follicles. During ovarian development in vivo, Sohlh2, and c-kit exhibited similar expression patterns to BMP4 and pSMAD1/5/8 in primordial follicles. The present studies suggest that BMP4/SMAD signaling pathway initiate primordial follicle growth and prevented oocyte apoptosis via up-regulation of Sohlh2 and c-kit. Mol. Reprod. Dev. 80: 7078, 2013. (c) 2012 Wiley Periodicals, Inc.
机译:骨形态发生蛋白4(BMP4)对于原始卵泡的发育是必不可少的,尽管其基本机制尚不清楚。通过使用培养的卵巢,研究了BMP4的作用和潜在的信号转导途径。在不存在(对照)或存在BMP4(100ng / ml)的情况下,将3天大的雌性小鼠幼仔的卵巢保持在器官培养物中。在不同的培养时间,通过卵泡计数和TUNEL标记检测BMP4对原始卵泡生长和存活的影响。磷酸SMAD1 / 5/8,Sohlh2和c-kit的表达通过免疫组织化学,RT-PCR和蛋白质印迹法进行了测量。还进行了免疫组织化学以确定卵巢发育期间体内的BMP4,pSMAD1 / 5/8,Sohlh2和c-kit的表达模式。结果显示,用BMP4处理卵巢会导致原始卵泡向原始卵泡的转换显着增加(P <0.05)。用BMP4处理的原始卵泡的卵母细胞也不太可能发生凋亡。 BMP4增强了SMAD1 / 5/8的磷酸化,并上调了原始卵泡中Sohlh2和c-kit的表达。在体内卵巢发育过程中,Sohlh2和c-kit在原始卵泡中表现出与BMP4和pSMAD1 / 5/8类似的表达模式。本研究表明,BMP4 / SMAD信号通路可通过上调Sohlh2和c-kit来启动原始卵泡生长并阻止卵母细胞凋亡。大声笑责备。开发人员80:7078,2013.(c)2012威利期刊公司

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号