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miR-181a-regulated pathways in T-cell differentiation and aging

Authors
Kim, ChulwooYe, ZhongdeWeyand, Cornelia M.Goronzy, Jorg J.
Issue Date
15-6월-2021
Publisher
BMC
Keywords
Infectious disease; Memory T cells; Replication stress; T cell activation; T cell aging; T cell differentiation; Vaccine; miR-181a; microRNA
Citation
IMMUNITY & AGEING, v.18, no.1
Indexed
SCIE
SCOPUS
Journal Title
IMMUNITY & AGEING
Volume
18
Number
1
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/137301
DOI
10.1186/s12979-021-00240-1
ISSN
1742-4933
Abstract
MicroRNAs (miRNAs) are regulatory noncoding RNAs important for many aspects of cellular processes including cell differentiation and proliferation. Functions of numerous miRNAs have been identified in T cells, with miR-181a regulating T cell activation thresholds during thymic T cell development and during activation of peripheral T cells. Intriguingly, miR-181a is implicated in defective antiviral and vaccine responses in older individuals, as its expression declines in naive T cells with increasing age. Here, we review the pathways that are regulated by miR-181a and that explain the unique role of miR-181a in T cell development, T cell activation and antiviral T cell responses. These studies provide a framework for understanding how a decline in miR-181a expression in T cells could contribute to age-related defects in adaptive immunity. We furthermore review the mechanisms that cause the age-related decline in miR-181a expression and discuss the potential of restoring miR-181a expression or targeting miR-181a-regulated pathways to improve impaired T cell responses in older individuals.
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