Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Aug:29:29-37.
doi: 10.1016/j.coi.2014.03.006. Epub 2014 Apr 25.

Effect of aging on microRNAs and regulation of pathogen recognition receptors

Affiliations
Review

Effect of aging on microRNAs and regulation of pathogen recognition receptors

Fabiola Olivieri et al. Curr Opin Immunol. 2014 Aug.

Abstract

Immunosenescence is the multifactorial age-associated immune deteriorization that leads to increased susceptibility to infections and decreased responses to vaccines. Recent studies have shown a fundamental role for microRNAs (miRNAs) in regulating immune responses, and nearly all the miRNAs involved in immune regulation show modulation during aging. Aging-associated miRNAs are largely negative regulators of the immune innate response and target central nodes of aging-associated networks, in particular, NF-κB, the downstream effector of TLR signals that leads to induction of proinflammatory responses. Multiple miRNAs have been reported to share similar regulatory activity. Here we review miRNA regulation of human innate immune recognition in aging, including both activation and resolution of inflammation, critical issues in detection, and areas of active investigation into our understanding of immunosenescence.

PubMed Disclaimer

Figures

Figure 1
Figure 1. Some of the most relevant miRs involved in restraining the activation of Pathogen Recognition Receptor (TLRs, NLRs, RLRs) and pro-inflammatory signalling pathways
Schematic representation of recognition receptors (TLRs, NLRs, RLRs) and signalling intermediates that are regulated by miRNAs.

References

    1. Arnold CR, Wolf J, Brunner S, Herndler-Brandstetter D, Grubeck-Loebenstein B. Gain and loss of T cell subsets in old age--age-related reshaping of the T cell repertoire. J Clin Immunol. 2011;31:137–146. - PubMed
    1. Frasca D, Diaz A, Romero M, Landin AM, Blomberg BB. Age effects on B cells and humoral immunity in humans. Ageing Res Rev. 2011;10:330–335. - PMC - PubMed
    1. Shaw AC, Goldstein DG, Montgomery RR. Dysregulated innate immune function in aging. Nat. Rev. Immunol. 2013;13:875–887. - PMC - PubMed
    1. Franceschi C, Capri M, Monti D, Giunta S, Olivieri F, Sevini F, Panourgia MP, Invidia L, Celani L, Scurti M, Cevenini E, Castellani GC, Salvioli S. Inflammaging and anti-inflammaging: a systemic perspective on aging and longevity emerged from studies in humans. Mech Ageing Dev. 2007;128:92–105. - PubMed
    1. Jung HJ, Suh Y. MicroRNA in Aging: From Discovery to Biology. Curr Genomics. 2012;13:548–557. - PMC - PubMed

Publication types