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卵母细胞凋亡的调控:从基因敲除小鼠看。

Regulation of Oocyte Apoptosis: A View from Gene Knockout Mice.

机构信息

Department of Biological Sciences, Kent State University, Room 108, Kent, OH 44242, USA.

出版信息

Int J Mol Sci. 2023 Jan 10;24(2):1345. doi: 10.3390/ijms24021345.

Abstract

Apoptosis is a form of programmed cell death that plays a critical role in cellular homeostasis and development, including in the ovarian reserve. In humans, hundreds of thousands of oocytes are produced in the fetal ovary. However, the majority die by apoptosis before birth. After puberty, primordial follicles develop into mature follicles. While only a large dominant follicle is selected to ovulate, smaller ones undergo apoptosis. Despite numerous studies, the mechanism of oocyte death at the molecular level remains elusive. Over the last two and a half decades, many knockout mouse models disrupting key genes in the apoptosis pathway have been generated. In this review, we highlight some of the phenotypes and discuss distinct and overlapping roles of the apoptosis regulators in oocyte death and survival. We also review how the transcription factor p63 and its family members may trigger oocyte apoptosis in response to DNA damage.

摘要

细胞凋亡是一种程序性细胞死亡形式,在细胞内稳态和发育中起着关键作用,包括在卵巢储备中。在人类中,数以十万计的卵母细胞在胎儿卵巢中产生。然而,在出生前,大多数卵母细胞通过细胞凋亡死亡。青春期后,原始卵泡发育成成熟卵泡。虽然只有一个大的优势卵泡被选择排卵,但较小的卵泡会发生凋亡。尽管进行了大量研究,但卵母细胞死亡的分子机制仍然难以捉摸。在过去的二十五年中,已经产生了许多破坏凋亡途径中关键基因的敲除小鼠模型。在这篇综述中,我们强调了一些表型,并讨论了凋亡调节剂在卵母细胞死亡和存活中的独特和重叠作用。我们还回顾了转录因子 p63 及其家族成员如何在应对 DNA 损伤时引发卵母细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f3c/9861590/1e909b3f1e20/ijms-24-01345-g001.jpg

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