p300 Maintains Primordial Follicle Activation by Repressing VEGFA Transcription.

IF 5 2区 生物学 Q2 CELL BIOLOGY
Meina He, Yaoyun Liang, Xiaoran Nie, Tuo Zhang, Danqing Zhao, Jixian Zhang, Huan Lin, Zhirui Zeng, Xingyu Song, Yitong Wang, Shiling Ran, Shuyun Zhao, Tengxiang Chen, Chunlin Zhang, Zhanhui Feng
{"title":"p300 Maintains Primordial Follicle Activation by Repressing <i>VEGFA</i> Transcription.","authors":"Meina He, Yaoyun Liang, Xiaoran Nie, Tuo Zhang, Danqing Zhao, Jixian Zhang, Huan Lin, Zhirui Zeng, Xingyu Song, Yitong Wang, Shiling Ran, Shuyun Zhao, Tengxiang Chen, Chunlin Zhang, Zhanhui Feng","doi":"10.1152/ajpcell.00198.2024","DOIUrl":null,"url":null,"abstract":"<p><p>During the reproductive life, most primordial follicles remain dormant for years or decades, while some are progressively activated for development. <u>Misactivation of primordial follicles can cause ovarian diseases,</u> <u>for example,</u> <u>premature ovarian insufficiency (POI).</u> Our results show that p300 expression increased with primordial follicle activation. Using a p300 inhibitor resulted in premature activation of primordial follicles in cultured mouse ovaries. Conversely, the ratio of primordial follicle activation was markedly decreased upon culturing with the p300 agonist. Furthermore, p300 regulated primordial follicle activation by inhibiting <i>Vegfa</i> transcription in granulosa cells. Additionally, this study was extended to potential clinical applications, showing that short-term treatment with a p300 inhibitor <i>in vitro</i> significantly increased primordial follicle activation in newborn mouse ovaries after dorsal kidney membrane transplantation in female NSG mice. Our results revealed that p300 controls the activation of primordial follicles in mammalian ovaries.</p>","PeriodicalId":7585,"journal":{"name":"American journal of physiology. Cell physiology","volume":" ","pages":""},"PeriodicalIF":5.0000,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Cell physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1152/ajpcell.00198.2024","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

During the reproductive life, most primordial follicles remain dormant for years or decades, while some are progressively activated for development. Misactivation of primordial follicles can cause ovarian diseases, for example, premature ovarian insufficiency (POI). Our results show that p300 expression increased with primordial follicle activation. Using a p300 inhibitor resulted in premature activation of primordial follicles in cultured mouse ovaries. Conversely, the ratio of primordial follicle activation was markedly decreased upon culturing with the p300 agonist. Furthermore, p300 regulated primordial follicle activation by inhibiting Vegfa transcription in granulosa cells. Additionally, this study was extended to potential clinical applications, showing that short-term treatment with a p300 inhibitor in vitro significantly increased primordial follicle activation in newborn mouse ovaries after dorsal kidney membrane transplantation in female NSG mice. Our results revealed that p300 controls the activation of primordial follicles in mammalian ovaries.

p300 通过抑制 VEGFA 转录维持原始卵泡的活化。
在生殖过程中,大多数原始卵泡会休眠数年或数十年,而一些原始卵泡会逐渐被激活发育。原始卵泡的错误激活可导致卵巢疾病,如卵巢早衰(POI)。我们的研究结果表明,p300的表达随着原始卵泡的激活而增加。在培养的小鼠卵巢中,使用 p300 抑制剂会导致原始卵泡过早激活。相反,使用 p300 激动剂培养小鼠卵巢时,原始卵泡活化的比例明显降低。此外,p300 通过抑制颗粒细胞中 Vegfa 的转录来调节原始卵泡的活化。此外,这项研究还扩展到了潜在的临床应用,结果表明,在体外用p300抑制剂短期处理雌性NSG小鼠背肾膜移植后,新生小鼠卵巢中原始卵泡的活化明显增加。我们的研究结果表明,p300 控制着哺乳动物卵巢中原始卵泡的活化。
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 求助全文
来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信