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Sci. STKE, 4 January 2005 EDITORS' CHOICEIMMUNOLOGY Dying for That Touch of MINK?
During development in the thymus, T cells with T cell receptors (TCRs) that bind major histocompatibility complex (MHC)-self peptide complexes with low affinity (which recognize foreign antigens) survive, and T cells with TCRs that bind MHC-self peptide complexes with high affinity (which recognize self-antigens) are eliminated. The survival pathways activated by low-affinity binding depend on activation of extracellular signal-regulated kinase (ERK), whereas the early steps through which high-affinity binding leads to apoptosis during "negative selection" are less well understood (see Palmer). McCarty et al. performed serial analysis of genes expressed in developing mouse thymocytes and found that expression of the misshapen-Nck-interacting kinase (NIK)-related kinase (MINK, a MAPKKKK) increased early in thymocyte development and then decreased after selection took place. Mice in which thymocyte MINK was knocked down through RNA interference showed increased numbers of postselection thymocytes; moreover, the deletion of autoreactive thymocytes was impaired. Western analysis combined with immunoprecipitation indicated that TCR activation in vitro promoted the association of MINK with Nck and CD3 N. McCarty, S. Paust, K. Ikizawa, I. Dan, X. Li, H. Cantor, Signaling by the MINK is essential in the negative selection of autoreactive thymocytes. Nat. Immunol. 6, 65-72 (2005). [PubMed] E. Palmer, Signaling negative selection: Is MINK the missing link? Nat. Immunol. 6, 9-10 (2005). [PubMed]
Citation: Dying for That Touch of MINK? Sci. STKE 2005, tw4 (2005). |
Science Signaling. ISSN 1937-9145 (pre-2008: Science's STKE. ISSN 1525-8882)