生理衰老小鼠雌性生殖衰老的特征

IF 17 Q1 CELL BIOLOGY
Julia L. Balough, Shweta S. Dipali, Karen Velez, T. Rajendra Kumar, Francesca E. Duncan
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引用次数: 0

摘要

女性生殖轴是最早衰老的器官系统之一,这对生育能力和整体健康都有影响。在此,我们基于广泛使用的生理衰老小鼠模型的研究,全面概述了雌性生殖衰老在生殖器官、组织和细胞方面的生物学过程,并描述了这些表型的基础机制。总的来说,衰老与下丘脑-垂体-卵巢轴的失调、卵巢基质的扰动、卵子数量和质量的减少以及子宫形态和功能的改变有关,从而导致受精能力下降和胚胎发育受损。最终,这些与年龄相关的表型有助于改变妊娠结局和后代的不良后果。保守的衰老机制,以及生殖系统特有的机制,是这些表型的基础。对这些机制的了解将导致治疗方法的发展,以延长女性生殖寿命,支持内分泌功能和整体健康。女性生殖系统老化会影响生育能力和整体健康。本文通过对小鼠生理衰老模型的研究,综述了雌性生殖衰老的生物学过程,并描述了这些表型背后的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hallmarks of female reproductive aging in physiologic aging mice

Hallmarks of female reproductive aging in physiologic aging mice
The female reproductive axis is one of the first organ systems to age, which has consequences for fertility and overall health. Here, we provide a comprehensive overview of the biological process of female reproductive aging across reproductive organs, tissues and cells based on research with widely used physiologic aging mouse models, and describe the mechanisms that underpin these phenotypes. Overall, aging is associated with dysregulation of the hypothalamic–pituitary–ovarian axis, perturbations of the ovarian stroma, reduced egg quantity and quality, and altered uterine morphology and function that contributes to reduced capacity for fertilization and impaired embryo development. Ultimately, these age-related phenotypes contribute to altered pregnancy outcomes and adverse consequences in offspring. Conserved mechanisms of aging, as well as those unique to the reproductive system, underlie these phenotypes. The knowledge of such mechanisms will lead to development of therapeutics to extend female reproductive longevity and support endocrine function and overall health. Female reproductive system aging has consequences for fertility and overall health. In this Review, the authors provide a comprehensive overview of the biological process of female reproductive aging based on research with physiologic aging mouse models, and describe the mechanisms that underlie these phenotypes.
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CiteScore
14.70
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