4.5 Article

miR-148a is upregulated by Twist1 and T-bet and promotes Th1-cell survival by regulating the proapoptotic gene Bim

期刊

EUROPEAN JOURNAL OF IMMUNOLOGY
卷 45, 期 4, 页码 1192-1205

出版社

WILEY
DOI: 10.1002/eji.201444633

关键词

Bim; miR-148a; T-bet; Th1; Twist1

资金

  1. Deutsche Forschungsgemeinschaft [GRK1121, SFB 618, SFB 650, SFB 633, SFB TR52]
  2. Deutsche Forschungsgemeinschaft (BSRT) [DFG-GSC203]
  3. International Max Planck Research School for Infectious Diseases and Immunology
  4. IMI JU [115241]
  5. FORSYS (Forschungseinheiten zur Systembiologie)
  6. e:Bio - Innovationswettbewerb Systembiologie program of the Federal Ministry of Education
  7. Interdisciplinary Center for Clinical Research (IZKF) Erlangen [D7]
  8. Deutsche Forschungsgemeinschaft (DFG) [GRK1660, FOR832 (JA968/4), TRR130]
  9. ERC [268987]
  10. European Research Council (ERC) [268987] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Repeatedly activated T helper 1 (Th1) cells present during chronic inflammation can efficiently adapt to the inflammatory milieu, for example, by expressing the transcription factor Twist1, which limits the immunopathology caused by Th1 cells. Here, we show that in repeatedly activated murine Th1 cells, Twist1 and T-bet induce expression of microRNA-148a (miR-148a). miR-148a regulates expression of the proapoptotic gene Bim, resulting in a decreased Bim/Bcl2 ratio. Inhibition of miR-148a by antagomirs in repeatedly activated Th1 cells increases the expression of Bim, leading to enhanced apoptosis. Knockdown of Bim expression by siRNA in miR-148a antagomir-treated cells restores viability of the Th1 cells, demonstrating that miR-148a controls survival by regulating Bim expression. Thus, Twist1 and T-bet not only control the differentiation and function of Th1 cells, but also their persistence in chronic inflammation.

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