Repetitive element transcript accumulation is associated with inflammaging in humans
Meghan E. Smith, Devin Wahl, Alyssa N. Cavalier, Gabriella T. Mcwilliams, Matthew J. Rossman, Gregory R. Giordano, Angela D. Bryan, Douglas R. Seals and Thomas J. Larocca
Geriatrics & Gerontology Life Sciences & Biomedicine Science & Technology
Chronic, low-grade inflammation increases with aging, contributing to functional declines and diseases that reduce healthspan. Growing evidence suggests that transcripts from repetitive elements (RE) in the genome contribute to this "inflammaging" by stimulating innate immune activation, but evidence of RE-associated inflammation with aging in humans is limited. Here, we present transcriptomic and clinical data showing that RE transcript levels are positively related to gene expression of innate immune sensors, and to serum interleukin 6 (a marker of systemic inflammation), in a large group of middle-aged and older adults. We also: (1) use transcriptomics and whole-genome bisulfite (methylation) sequencing to show that many RE may be hypomethylated with aging, and that aerobic exercise, a healthspan-extending intervention, reduces RE transcript levels and increases RE methylation in older adults; and (2) extend our findings in a secondary dataset demonstrating age-related changes in RE chromatin accessibility. Collectively, our data support the idea that age-related RE transcript accumulation may play a role in inflammaging in humans, and that RE dysregulation with aging may be due in part to upstream epigenetic changes.
Repetitive element transcript accumulation is associated with inflammaging in humans
Creators
Meghan E. Smith - Colorado State University
Devin Wahl - Colorado State University
Alyssa N. Cavalier - Colorado State University
Gabriella T. Mcwilliams - Colorado State University
Matthew J. Rossman - University of Colorado Boulder
Gregory R. Giordano - University of Colorado Boulder
Angela D. Bryan - University of Colorado Boulder
Douglas R. Seals - University of Colorado Boulder
Thomas J. Larocca - Colorado State University
Publication Details
GeroScience
Publisher
Springer Nature
Number of pages
17
Grant note
National Institute on Aging; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute on Aging (NIA)
Resource Type
Journal article
Language
English
Academic Unit
Health Sciences
Web of Science ID
WOS:001205246500001
Scopus ID
2-s2.0-85190802992
Other Identifier
991021894713004721
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Collaboration types
Domestic collaboration
Web of Science research areas
Geriatrics & Gerontology
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