灵长类动物
非人灵长类
神经科学
认知
转录组
疾病
生物
心理学
认知功能衰退
人脑
衰老的大脑
人口
基因
基因表达
医学
痴呆
进化生物学
遗传学
病理
环境卫生
作者
Kenneth L. Chiou,Alex R. DeCasien,Katherina P. Rees,Camille Testard,Cailyn H. Spurrell,Aishwarya A. Gogate,Hannah A. Pliner,Sébastien Tremblay,Arianne Mercer,Connor J. Whalen,Josué E. Negrón-Del Valle,Mareike C. Janiak,Samuel E. Bauman,Olga González,Nicole R. Compo,Michala K. Stock,Angelina V. Ruiz-Lambides,Melween I. Martínez,Melissa A. Wilson,Amanda Dawn Melin
标识
DOI:10.1038/s41593-022-01197-0
摘要
Aging is accompanied by a host of social and biological changes that correlate with behavior, cognitive health and susceptibility to neurodegenerative disease. To understand trajectories of brain aging in a primate, we generated a multiregion bulk (N = 527 samples) and single-nucleus (N = 24 samples) brain transcriptional dataset encompassing 15 brain regions and both sexes in a unique population of free-ranging, behaviorally phenotyped rhesus macaques. We demonstrate that age-related changes in the level and variance of gene expression occur in genes associated with neural functions and neurological diseases, including Alzheimer's disease. Further, we show that higher social status in females is associated with younger relative transcriptional ages, providing a link between the social environment and aging in the brain. Our findings lend insight into biological mechanisms underlying brain aging in a nonhuman primate model of human behavior, cognition and health.
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