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Mol Immunol. 2020 Apr;120:67-73. doi: 10.1016/j.molimm.2020.01.023. Epub 2020 Feb 18.

Non-coding RNAs in CD8 T cell biology.

Author information

1
National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, 20814, United States. Electronic address: alex.wells@nih.gov.
2
Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, 01003, United States. Electronic address: pobezinskaya@umass.edu.
3
Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, 01003, United States. Electronic address: lpobezinsky@umass.edu.

Abstract

CD8 T cells are among the most vigorous soldiers of the immune system that fight viral infections and cancer. CD8 T cell development, maintenance, activation and differentiation are under the tight control of multiple transcriptional and post-transcriptional networks. Over the last two decades it has become clear that non-coding RNAs (ncRNAs), which consist of microRNAs (miRNAs) and long ncRNAs (lncRNAs), have emerged as global biological regulators. While our understanding of the function of specific miRNAs has increased since the discovery of RNA interference, it is still very limited, and the field of lncRNAs is just starting to blossom. Here we will summarize our knowledge on the role of ncRNAs in CD8 T cell biology, including differentiation into memory and exhausted cells.

KEYWORDS:

CTL; Effector; Exhaustion; Memory; Naïve; lncRNA; miRNA

PMID:
32085976
PMCID:
PMC7093237
[Available on 2021-04-01]
DOI:
10.1016/j.molimm.2020.01.023

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