Posttranscriptional and Translational Control of Gene Regulation in CD4+ T Cell Subsets

被引:12
作者
Istomine, Roman
Pavey, Nils
Piccirillo, Ciriaco A.
机构
[1] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Program Infect Dis & Immun Global Hlth, Translat Immunol Unit, Res Inst,Hlth Ctr, Montreal, PQ H4A 3J1, Canada
[3] McGill Univ, Federat Clin Immunol Soc Ctr Excellence, Montreal, PQ H3H 2R9, Canada
[4] McGill Univ, Ctr Hlth, Res Inst, Montreal, PQ H3H 2R9, Canada
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; MESSENGER-RNA; TRANSCRIPTION FACTOR; LYMPHOCYTE DEVELOPMENT; TH17; DIFFERENTIATION; PROTEIN ABUNDANCE; EFFECTOR FUNCTION; REG-CELLS; EXPRESSION; ACTIVATION;
D O I
10.4049/jimmunol.1501337
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune system is under strict regulatory control to ensure homeostasis of inflammatory responses, lying dormant when not needed but quick to act when called upon. Small changes in gene expression can lead to drastic changes in lineage commitment, cellular function, and immunity. Conventional assessment of these changes centered on the analysis of mRNA levels through a variety of methodologies, including microarrays. However, mRNA synthesis does not always correlate directly to protein synthesis and downstream functional activity. Work conducted in recent years has begun to shed light on the various posttranscriptional changes that occur in response to a dynamic external environment that a given cell type encounters. We provide a critical review of key posttranscriptional mechanisms (i.e., microRNA) and translational mechanisms of regulation of gene expression in the immune system, with a particular emphasis on these regulatory processes in various CD4(+) T cell subsets.
引用
收藏
页码:533 / 540
页数:8
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