4.1 Article

MicroRNA Regulation of T-Lymphocyte Immunity: Modulation of Molecular Networks Responsible for T-Cell Activation, Differentiation, and Development

期刊

CRITICAL REVIEWS IN IMMUNOLOGY
卷 33, 期 5, 页码 435-476

出版社

BEGELL HOUSE INC
DOI: 10.1615/CritRevImmunol.2013006858

关键词

microRNA; T cell; T-cell activation; T-cell function; T-cell development; microRNA regulation of molecular networks

资金

  1. NIH [R01 AI081757, U19 A1063603, U01 GM094653, U01 A1084146]
  2. NATIONAL CENTER FOR RESEARCH RESOURCES [TL1RR025772] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [U01AI084146, R01AI081757, U19AI063603] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [U01GM094653] Funding Source: NIH RePORTER

向作者/读者索取更多资源

MicroRNAs (miRNA) are a class of small non-coding RNAs that constitute an essential and evolutionarily conserved mechanism for post-transcriptional gene regulation. Multiple miRNAs have been described to play key roles in T-lymphocyte development, differentiation, and function. In this review, we highlight the current literature regarding the differential expression of miRNAs in various models of murine and human T-cell biology. We emphasize mechanistic understandings of miRNA regulation of thyrnocyte development, T-cell activation, and differentiation into effector and memory subsets. We describe the participation of miRNAs in complex regulatory circuits shaping T-cell proteomes in a context-dependent manner. It is striking that some miRNAs regulate multiple processes, while others only appear in limited functional contexts. It is also evident that the expression and function of specific miRNAs can differ between murine and human systems. Ultimately, it is not always correct to simplify the complex events of T-cell biology into a model driven by only one or two master regulator miRNAs. In reality, T-cell activation and differentiation involve the expression of multiple miRNAs with many mRNA targets; thus, the true extent of miRNA regulation of T-cell biology is likely far more vast than currently appreciated.

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