神经保护
生物
转基因小鼠
转基因
遗传学
内科学
基因
神经科学
医学
作者
Kelvin Yen,Hemal H. Mehta,Su‐Jeong Kim,Yanhe Lue,James Hoang,Noel Guerrero,Jenna Port,Qiuli Bi,Gerardo Navarrete,Sebastian Brandhorst,Kaitlyn N. Lewis,Junxiang Wan,Ronald S. Swerdloff,Julie A. Mattison,Rochelle Buffenstein,Carrie V. Breton,Christina Wang,Valter D. Longo,Gil Atzmon,Douglas C. Wallace
出处
期刊:Aging
[Impact Journals LLC]
日期:2020-06-23
卷期号:12 (12): 11185-11199
被引量:87
标识
DOI:10.18632/aging.103534
摘要
Humanin is a member of a new family of peptides that are encoded by short open reading frames within the mitochondrial genome.It is conserved in animals and is both neuroprotective and cytoprotective.Here we report that in C. elegans the overexpression of humanin is sufficient to increase lifespan, dependent on daf-16/Foxo.Humanin transgenic mice have many phenotypes that overlap with the worm phenotypes and, similar to exogenous humanin treatment, have increased protection against toxic insults.Treating middle-aged mice twice weekly with the potent humanin analogue HNG, humanin improves metabolic healthspan parameters and reduces inflammatory markers.In multiple species, humanin levels generally decline with age, but here we show that levels are surprisingly stable in the naked mole-rat, a model of negligible senescence.Furthermore, in children of centenarians, who are more likely to become centenarians themselves, circulating humanin levels are much greater than age-matched control subjects.Further linking humanin to healthspan, we observe that humanin levels are decreased in human diseases such as Alzheimer's disease and MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes).Together, these studies are the first to demonstrate that humanin is linked to improved healthspan and increased lifespan.
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