4.7 Article

An essential role for c-FLIP in the efficient development of mature T lymphocytes

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JOURNAL OF EXPERIMENTAL MEDICINE
卷 202, 期 3, 页码 395-404

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ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20050117

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  1. NCI NIH HHS [R01 CA092123, CA92123] Funding Source: Medline

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Apoptosis-related genes play important roles in thymocyte maturation. We show that cellular FLICE-like inhibitory protein (c-FLIP), a procaspase-8-like apoptotic regulator, plays an essential role in the efficient development of mature T lymphocytes. Mice conditionally lacking c-FLIP in T lymphocytes display severe defects in the development of mature T cells, as indicated by a dramatically reduced number of CD4(+) and CD8(+) T cells in the spleen and lymph nodes of mutant mice. The impaired T lymphocyte maturation in c-FLIP conditional knockout mice occurs at the single-positive thymocyte stage and may be caused by enhanced apoptosis in vivo. Moreover, although c-FLIP has been implicated in T cell receptor signaling through nuclear factor (NF)-kappa B and Erk pathways, activation of NF-kappa B and Erk in c-FLIP-deficient thymocytes appears largely intact. Collectively, our data suggest that the primary role of c-FLIP in thymocyte maturation is to protect cells from apoptosis.

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