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Changes in the Transcriptome of Human Astrocytes Accompanying Oxidative Stress-Induced Senescence
Journal article   Open access   Peer reviewed

Changes in the Transcriptome of Human Astrocytes Accompanying Oxidative Stress-Induced Senescence

Elizabeth P. Crowe, Ferit Tuzer, Brian D. Gregory, Greg Donahue, Sager J. Gosai, Justin Cohen, Yuk Y. Leung, Emre Yetkin, Raffaella Nativio, Li-San Wang, …
Frontiers in aging neuroscience, v 8, pp 208-208
31 Aug 2016
PMID: 27630559
url
https://doi.org/10.3389/fnagi.2016.00208View
Published, Version of Record (VoR)CC BY V4.0 Open

Abstract

astrocyte function astrocyte senescence brain aging brain oxidative stress Neuroscience RNA sequencing
Aging is a major risk factor for many neurodegenerative disorders. A key feature of aging biology that may underlie these diseases is cellular senescence. Senescent cells accumulate in tissues with age, undergo widespread changes in gene expression, and typically demonstrate altered, pro-inflammatory profiles. Astrocyte senescence has been implicated in neurodegenerative disease, and to better understand senescence-associated changes in astrocytes, we investigated changes in their transcriptome using RNA sequencing. Senescence was induced in human fetal astrocytes by transient oxidative stress. Brain-expressed genes, including those involved in neuronal development and differentiation, were downregulated in senescent astrocytes. Remarkably, several genes indicative of astrocytic responses to injury were also downregulated, including glial fibrillary acidic protein and genes involved in the processing and presentation of antigens by major histocompatibility complex class II proteins, while pro-inflammatory genes were upregulated. Overall, our findings suggest that senescence-related changes in the function of astrocytes may impact the pathogenesis of age-related brain disorders.

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Collaboration types
Domestic collaboration
Web of Science research areas
Geriatrics & Gerontology
Neurosciences
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