GATA4: Regulation of expression and functions in goat granulosa cells

IF 1.9 2区 农林科学 Q2 AGRICULTURE, DAIRY & ANIMAL SCIENCE Domestic animal endocrinology Pub Date : 2024-05-23 DOI:10.1016/j.domaniend.2024.106859
Kexin Gao , Yeda Chen , Peijie Wang , Wenlin Chang , Binyun Cao , Liqiong Luo
{"title":"GATA4: Regulation of expression and functions in goat granulosa cells","authors":"Kexin Gao ,&nbsp;Yeda Chen ,&nbsp;Peijie Wang ,&nbsp;Wenlin Chang ,&nbsp;Binyun Cao ,&nbsp;Liqiong Luo","doi":"10.1016/j.domaniend.2024.106859","DOIUrl":null,"url":null,"abstract":"<div><p>GATA4 plays a pivotal role in the reproductive processes of mammals. However, the research on GATA4 in goat ovary is limited. This study aimed to study the expression and function of GATA4 in goat ovary. Utilizing real-time PCR and western blot analysis, we studied the expression and regulatory mechanisms of GATA4 in goat ovary and granulosa cells (GCs). We found that GATA4 was expressed in all follicle types in the goat ovary, with significantly higher levels in GCs of larger follicles (&gt;3 mm) compared to those in smaller follicles (&lt;3 mm). Additionally, we demonstrated that human chorionic gonadotrophin (hCG) induced <em>GATA4</em> mRNA expression via the activation of PKA, MEK, p38 MAPK, PKC, and PI3K pathways <em>in vitro</em>. Our study also showed that hCG suppressed the levels of miR-200b and miR-429, which in turn directly target GATA4, thereby modulating the basal and hCG-induced expression of GATA4. Functionally, we examined the effect of siRNA-mediated <em>GATA4</em> knockdown on cell proliferation and hormone secretion in goat GCs. Our results revealed that knockdown of <em>GATA4</em>, miR-200b, and miR-429 suppressed cell proliferation. Moreover, knockdown of <em>GATA4</em> decreased estradiol and progesterone production by inhibiting the promoter activities of <em>CYP11A1, CYP19A1, HSD3B,</em> and <em>StAR</em>. Collectively, our findings suggest a critical involvement of GATA4 in regulating goat GC survival and steroidogenesis.</p></div>","PeriodicalId":11356,"journal":{"name":"Domestic animal endocrinology","volume":"89 ","pages":"Article 106859"},"PeriodicalIF":1.9000,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Domestic animal endocrinology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0739724024000225","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 0

Abstract

GATA4 plays a pivotal role in the reproductive processes of mammals. However, the research on GATA4 in goat ovary is limited. This study aimed to study the expression and function of GATA4 in goat ovary. Utilizing real-time PCR and western blot analysis, we studied the expression and regulatory mechanisms of GATA4 in goat ovary and granulosa cells (GCs). We found that GATA4 was expressed in all follicle types in the goat ovary, with significantly higher levels in GCs of larger follicles (>3 mm) compared to those in smaller follicles (<3 mm). Additionally, we demonstrated that human chorionic gonadotrophin (hCG) induced GATA4 mRNA expression via the activation of PKA, MEK, p38 MAPK, PKC, and PI3K pathways in vitro. Our study also showed that hCG suppressed the levels of miR-200b and miR-429, which in turn directly target GATA4, thereby modulating the basal and hCG-induced expression of GATA4. Functionally, we examined the effect of siRNA-mediated GATA4 knockdown on cell proliferation and hormone secretion in goat GCs. Our results revealed that knockdown of GATA4, miR-200b, and miR-429 suppressed cell proliferation. Moreover, knockdown of GATA4 decreased estradiol and progesterone production by inhibiting the promoter activities of CYP11A1, CYP19A1, HSD3B, and StAR. Collectively, our findings suggest a critical involvement of GATA4 in regulating goat GC survival and steroidogenesis.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
GATA4:山羊颗粒细胞中的表达和功能调控
GATA4 在哺乳动物的生殖过程中发挥着关键作用。然而,有关山羊卵巢中 GATA4 的研究还很有限。本研究旨在研究 GATA4 在山羊卵巢中的表达和功能。通过实时 PCR 和 Western 印迹分析,我们研究了 GATA4 在山羊卵巢和颗粒细胞(GCs)中的表达和调控机制。我们发现,GATA4在山羊卵巢的所有卵泡类型中都有表达,与小卵泡(3 mm)相比,大卵泡(3 mm)的颗粒细胞中的GATA4水平明显更高。此外,我们还证明了人绒毛膜促性腺激素(hCG)在体外通过激活 PKA、MEK、p38 MAPK、PKC 和 PI3K 途径诱导 GATA4 mRNA 的表达。我们的研究还显示,hCG抑制了miR-200b和miR-429的水平,而miR-200b和miR-429又直接靶向GATA4,从而调节了GATA4的基础表达和hCG诱导的表达。在功能上,我们研究了 siRNA 介导的 GATA4 敲除对山羊 GC 细胞增殖和激素分泌的影响。结果发现,敲除 GATA4、miR-200b 和 miR-429 会抑制细胞增殖。此外,敲除 GATA4 还能抑制 CYP11A1、CYP19A1、HSD3B 和 StAR 的启动子活性,从而减少雌二醇和孕酮的分泌。总之,我们的研究结果表明,GATA4 在调节山羊 GC 的存活和类固醇生成方面起着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Domestic animal endocrinology
Domestic animal endocrinology 农林科学-奶制品与动物科学
CiteScore
5.50
自引率
4.80%
发文量
58
审稿时长
31 days
期刊介绍: Domestic Animal Endocrinology publishes scientific papers dealing with the study of the endocrine physiology of domestic animal species. Those manuscripts utilizing other species as models for clinical or production problems associated with domestic animals are also welcome. Topics covered include: Classical and reproductive endocrinology- Clinical and applied endocrinology- Regulation of hormone secretion- Hormone action- Molecular biology- Cytokines- Growth factors
期刊最新文献
Effect of short-term dopamine reduction on insulin sensitivity and post-prandial insulin and glucose responses in Standardbred horses Effects of rumen metabolite butyric acid on bovine skeletal muscle satellite cells proliferation, apoptosis and transcriptional states during myogenic differentiation Physiological and metabolic effects of short-term dopamine reduction in healthy horses using a tyrosine hydroxylase inhibitor (alpha-methyl-para-tyrosine) Improving survival and growth of caprine preantral follicles cultured in medium commonly used for MSC: Role of oxidative stress regulation and epigenetic changes Editorial Board
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1