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 PMID:9806643  

Differentiation of CD4+ T cells to Th1 cells requires MAP kinase JNK2.

D D Yang | D Conze | A J Whitmarsh | T Barrett | R J Davis | M Rincón | R A Flavell
Immunity | 1998

Precursor CD4+ T cells develop into effector Th1 and Th2 cells that play a central role in the immune response. We show that the JNK MAP kinase pathway is induced in Th1 but not in Th2 effector cells upon antigen stimulation. Further, the differentiation of precursor CD4+ T cells into effector Th1 but not Th2 cells is impaired in JNK2-deficient mice. The inability of IL-12 to differentiate JNK2-deficient CD4+ T cells fully into effector Th1 cells is caused by a defect in IFNgamma production during the early stages of differentiation. The addition of exogenous IFNgamma during differentiation restores IL-12-mediated Th1 polarization in the JNK2-deficient mice. The JNK MAP kinase signaling pathway, therefore, plays an important role in the balance of Th1 and Th2 immune responses.

Pubmed ID: 9806643

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Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: P01 AI36529
  • Agency: NCI NIH HHS, United States
    Id: P01 CA72009
  • Agency: NCI NIH HHS, United States
    Id: R01 CA65861

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Zeiss Sigma VP Scanning Electron Microscope (tool)

RRID:SCR_020928

ZEISS SIGMA VP field emission scanning electron microscope (FE-SEM) for imaging of non-conducting samples. It images of bacteria, cells, plants and organisms. Uses ATLAS software and can be combined with 3View technology from Gatan Inc.

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