| First Author | Chang CF | Year | 2012 |
| Journal | J Immunol | Volume | 189 |
| Issue | 2 | Pages | 721-31 |
| PubMed ID | 22675204 | Mgi Jnum | J:189558 |
| Mgi Id | MGI:5446107 | Doi | 10.4049/jimmunol.1103015 |
| Citation | Chang CF, et al. (2012) Polar opposites: Erk direction of CD4 T cell subsets. J Immunol 189(2):721-31 |
| abstractText | Effective immune responses depend upon appropriate T cell differentiation in accord with the nature of an infectious agent, and the contingency of differentiation depends minimally on TCR, coreceptor, and cytokine signals. In this reverse genetic study, we show that the MAPK Erk2 is not essential for T cell proliferation in the presence of optimum costimulation. Instead, it has opposite effects on T-bet and Gata3 expression and, hence, on Th1 and Th2 differentiation. Alternatively, in the presence of TGF-beta, the Erk pathway suppresses a large program of gene expression, effectively limiting the differentiation of Foxp3(+) regulatory T cells. In the latter case, the mechanisms involved include suppression of Gata3 and Foxp3, induction of Tbx21, phosphorylation of Smad2,3, and possibly suppression of Socs2, a positive inducer of Stat5 signaling. Consequently, loss of Erk2 severely impeded Th1 differentiation while enhancing the development of Foxp3(+)-induced T regulatory cells. Selected profiles of gene expression under multiple conditions of T cell activation illustrate the opposing consequences of Erk pathway signaling. |
