How engagement of surface T cell antigen receptors 'translates' into intracellular signal cascades remains vague. Genetic and biochemical experiments now allow modification of a model linking ligation of these receptors with CD3ɛ and other cytoplasmic signal-transduction 'machinery'.
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References
Minguenaeau, M. et al. Nat. Immunol. 9, 522–532 (2008).
Gil, D., Schamel, W.W., Montoya, M., Sanchez-Madrid, F. & Alarcon, B. Cell 109, 901–912 (2002).
Szymczak, A.L. et al. J. Immunol. 175, 270–275 (2005).
Sosinowski, T., Killeen, N. & Weiss, A. Immunity 15, 457–466 (2001).
Myers, M.D. et al. Nat. Immunol. 7, 57–66 (2006).
Van Laethem, F. et al. Immunity 27, 735–750 (2007).
Kesti, T. et al. J. Immunol. 179, 878–885 (2007).
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Maltzman, J., Koretzky, G. CD3ɛ: PeRuSing for positive selection. Nat Immunol 9, 457–459 (2008). https://doi.org/10.1038/ni0508-457
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DOI: https://doi.org/10.1038/ni0508-457