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雌性 XX 性染色体可提高衰老小鼠的存活率并延长其寿命。

Female XX sex chromosomes increase survival and extend lifespan in aging mice.

机构信息

Department of Neurology, Biomedical Sciences Graduate Program, and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California.

Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California.

出版信息

Aging Cell. 2019 Feb;18(1):e12871. doi: 10.1111/acel.12871. Epub 2018 Dec 17.

DOI:10.1111/acel.12871
PMID:30560587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6351820/
Abstract

Female longevity is observed in humans and much of the animal kingdom, but its causes remain elusive. Using a genetic manipulation that generates XX and XY mice, each with either ovaries or testes, we show that the female XX sex chromosome complement increases survival during aging in male and female mice. In combination with ovaries, it also extends lifespan. Understanding causes of sex-based differences in aging could lead to new pathways to counter age-induced decline in both sexes.

摘要

女性长寿现象存在于人类和大部分动物界,但具体原因仍难以捉摸。本研究采用遗传操作手段,构建了既有卵巢又有睾丸的 XX 和 XY 雌雄同体小鼠,结果显示 XX 性染色体在雌雄小鼠衰老过程中提高了存活率。XX 性染色体与卵巢联合作用还延长了寿命。探究性别差异在衰老过程中的作用机制可能为两性衰老相关疾病的防治提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc52/6351820/3f5d073a4c88/ACEL-18-e12871-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc52/6351820/87d3f256fdb5/ACEL-18-e12871-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc52/6351820/3f5d073a4c88/ACEL-18-e12871-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc52/6351820/87d3f256fdb5/ACEL-18-e12871-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc52/6351820/3f5d073a4c88/ACEL-18-e12871-g002.jpg

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Life history evolution, reproduction, and the origins of sex-dependent aging and longevity.生活史进化、繁殖以及性别依赖型衰老和长寿的起源。
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Stroke sensitivity in the aged: sex chromosome complement vs. gonadal hormones.
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Aging activates escape of the silent X chromosome in the female mouse hippocampus.衰老会激活雌性小鼠海马体中失活X染色体的逃逸。
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