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Regulatory roles of MicroRNA in shaping T cell function, differentiation and polarization.
Naqvi, Raza Ali; Datta, Manali; Khan, Samia Haseeb; Naqvi, Afsar R.
Afiliação
  • Naqvi RA; Department of Periodontics, College of Dentistry, University of Illinois at Chicago, Chicago 60612, IL, USA. Electronic address: naqvi@uic.edu.
  • Datta M; Amity Institute of Biotechnology, Amity University Rajasthan, Jaipur, Rajasthan, India.
  • Khan SH; Graduate School of Medicine, Science and Technology, Shinshu University, 8304 Minami-Minowa, Kami-Ina, Nagano 399-4598, Japan.
  • Naqvi AR; Department of Periodontics, College of Dentistry, University of Illinois at Chicago, Chicago 60612, IL, USA. Electronic address: afsarraz@uic.edu.
Semin Cell Dev Biol ; 124: 34-47, 2022 04.
Article em En | MEDLINE | ID: mdl-34446356
ABSTRACT
T lymphocytes are an integral component of adaptive immunity with pleotropic effector functions. Impairment of T cell activity is implicated in various immune pathologies including autoimmune diseases, AIDS, carcinogenesis, and periodontitis. Evidently, T cell differentiation and function are under robust regulation by various endogenous factors that orchestrate underlying molecular pathways. MicroRNAs (miRNA) are a class of noncoding, regulatory RNAs that post-transcriptionally control multiple mRNA targets by sequence-specific interaction. In this article, we will review the recent progress in our understanding of miRNA-gene networks that are uniquely required by specific T cell effector functions and provide miRNA-mediated mechanisms that govern the fate of T cells. A subset of miRNAs may act in a synergistic or antagonistic manner to exert functional suppression of genes and regulate pathways that control T cell activation and differentiation. Significance of T cell-specific miRNAs and their dysregulation in immune-mediated diseases is discussed. Exosome-mediated horizontal transfer of miRNAs from antigen presenting cells (APCs) to T cells and from one T cell to another T cell subset and their impact on recipient cell functions is summarized.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: MicroRNAs Idioma: En Revista: Semin Cell Dev Biol Assunto da revista: EMBRIOLOGIA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: MicroRNAs Idioma: En Revista: Semin Cell Dev Biol Assunto da revista: EMBRIOLOGIA Ano de publicação: 2022 Tipo de documento: Article