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Sci. STKE, 30 May 2006 EDITORS' CHOICEIMMUNOLOGY Keeping LAT Out
T cell anergy prevents self-reactive T cells that escape elimination in the thymus from responding. T cell anergy is associated with decreased interleukin 2 (IL-2) production and decreased proliferation in response to antigen-specific stimulation. In a cultured cell system and an in vivo model, Hundt et al. show that, although phosphorylation of the tyrosine kinase ZAP-70 is not impaired, phosphorylation of the ZAP-70 substrate linker of activated T cells (LAT) is decreased. LAT serves as a scaffold recruiting various downstream effectors to the immunological synapse. Thus, lack of LAT phosphorylation prevents activation of phospholipase C- M. Hundt, H. Tabata, M.-S. Jeon, K. Hayashi, Y. Tanaka, R. Krishna, L. De Giorgio, Y.-C. Liu, M. Fukata, A. Altman, Impaired activation and localization of LAT in anergic T cells as a consequence of a selective palmitoylation defect. Immunity 24, 513-522 (2006). [PubMed] N. Lineberry, C. G. Fathman, T cell anergy: Where it's LAT. Immunity 24, 501-503 (2006). [PubMed]
Citation: Keeping LAT Out. Sci. STKE 2006, tw177 (2006). The editors suggest the following Related Resources on Science sites:In Science Signaling
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Science Signaling. ISSN 1937-9145 (pre-2008: Science's STKE. ISSN 1525-8882)