Cellular Mechanisms and Modulation of Activin A- and Transforming Growth Factor β-Mediated Differentiation in Cultured Hen Granulosa Cells1

胆固醇侧链裂解酶 内科学 内分泌学 生物 转化生长因子 颗粒细胞 类固醇生成急性调节蛋白 促性腺激素 MAPK/ERK通路 受体 卵泡 生长因子 卵巢 信号转导 信使核糖核酸 细胞生物学 激素 医学 基因 细胞色素P450 新陈代谢 生物化学
作者
A. L. Johnson,J. T. Bridgham,Dori C. Woods
出处
期刊:Biology of Reproduction [Oxford University Press]
卷期号:71 (6): 1844-1851 被引量:49
标识
DOI:10.1095/biolreprod.104.032573
摘要

Undifferentiated granulosa cells from prehierarchal (6- to 8-mm-diameter) hen follicles express very low to undetectable levels of LH receptor (LH-R) mRNA, P450 cholesterol side chain cleavage (P450scc) enzyme activity, and steroidogenic acute regulatory (StAR) protein, and produce negligible progesterone, in vitro, following an acute (3-h) challenge with either FSH or LH. It has previously been established that culturing such cells with FSH for 18-20 h induces LH-R, P450scc, and StAR expression, which enables the initiation of progesterone production. The present studies were conducted to characterize the ability of activin and transforming growth factor (TGF) beta, both alone and in combination with FSH, to promote hen granulosa cell differentiation, in vitro. A 20-h culture of prehierarchal follicle granulosa cells with activin A or transforming growth factor beta (TGFbeta)1 increased LH-R mRNA levels compared with control cultured cells. Activin A and TGFbeta1 also promoted FSH-receptor (FSH-R) mRNA expression when combined with FSH treatment. Neither activin A nor TGFbeta1 alone stimulated progesterone production after 20 h culture. However, preculture with either factor for 20 h (to induce gonadotropin receptor mRNA expression) followed by a 3-h challenge with FSH or LH potentiated StAR expression and progesterone production compared with cells challenged with gonadotropin in the absence of activin A or TGFbeta1 preculture. Significantly, activation of the mitogen-activated protein (MAP) kinase pathway with transforming growth factor alpha (TGFalpha) (monitored by Erk phosphorylation) blocked TGFbeta1-induced LH-R expression, and this effect was associated with the inhibition of Smad2 phosphorylation. We conclude that a primary differentiation-inducing action of activin A and TGFbeta1 on hen granulosa cells from prehierarchal follicles is directed toward LH-R expression. Enhanced LH-R levels subsequently sensitize granulosa cells to LH, which in turn promotes StAR plus P450scc expression and subsequently an increase in P4 production. Significantly, the finding that TGFbeta signaling is negatively regulated by MAP kinase signaling is proposed to represent a mechanism that prevents premature differentiation of granulosa cells.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
unchanged完成签到,获得积分10
刚刚
rong发布了新的文献求助10
2秒前
TG303完成签到,获得积分10
7秒前
科研通AI5应助科研通管家采纳,获得10
7秒前
7秒前
SciGPT应助科研通管家采纳,获得10
7秒前
7秒前
7秒前
愤怒的咖啡完成签到,获得积分10
9秒前
急诊守夜人完成签到 ,获得积分10
11秒前
啥也不会完成签到 ,获得积分10
13秒前
小凯完成签到 ,获得积分10
15秒前
aabsd完成签到,获得积分10
17秒前
Lucas应助Syne_采纳,获得10
18秒前
老乡开下门吧完成签到 ,获得积分10
18秒前
千里烟泼完成签到,获得积分10
22秒前
18340312141完成签到,获得积分10
22秒前
长安完成签到,获得积分10
24秒前
玩命的平蓝完成签到 ,获得积分10
32秒前
Yang完成签到 ,获得积分10
33秒前
Tantan完成签到,获得积分10
35秒前
班小班完成签到,获得积分10
37秒前
马家辉完成签到,获得积分10
37秒前
桂花酒酿完成签到,获得积分10
39秒前
子羽完成签到,获得积分10
41秒前
Silieze完成签到,获得积分10
43秒前
luogan完成签到,获得积分10
44秒前
44秒前
爆米花应助Rewi_Zhang采纳,获得10
45秒前
45秒前
666发布了新的文献求助50
46秒前
再睡十分钟完成签到,获得积分10
46秒前
诸忆雪完成签到,获得积分10
47秒前
zly完成签到 ,获得积分10
49秒前
简单水蓉完成签到,获得积分10
50秒前
52秒前
柚子发布了新的文献求助10
52秒前
Diego完成签到,获得积分10
53秒前
53秒前
动人的怀柔完成签到,获得积分10
53秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
Периодизация спортивной тренировки. Общая теория и её практическое применение 310
Mixing the elements of mass customisation 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3779378
求助须知:如何正确求助?哪些是违规求助? 3324920
关于积分的说明 10220406
捐赠科研通 3040087
什么是DOI,文献DOI怎么找? 1668560
邀请新用户注册赠送积分活动 798721
科研通“疑难数据库(出版商)”最低求助积分说明 758522