cFLIP regulation of lymphocyte activation and development
Author:
Publisher
Springer Science and Business Media LLC
Subject
Energy Engineering and Power Technology,Fuel Technology
Link
http://www.nature.com/articles/nri1787.pdf
Reference119 articles.
1. Chang, D. W. et al. c-FLIPL is a dual function regulator for caspase-8 activation and CD95-mediated apoptosis. EMBO J. 21, 3704–3714 (2002). One of the first descriptions of the ability of cFLIP L to activate full-length caspase-8.
2. Micheau, O. & Tschopp, J. Induction of TNF receptor I-mediated apoptosis via two sequential signalling complexes. Cell 114, 181–190 (2003).
3. Kataoka, T. & Tschopp, J. N-terminal fragment of c-FLIPL processed by caspase 8 specifically interacts with TRAF2 and induces activation of the NF-κB signalling pathway. Mol. Cell. Biol. 24, 2627–2636 (2004). An important study showing that p43cFLIP can recruit TRAF2 more efficiently than cFLIP L . This might indicate that cFLIP L is an important caspase-8 substrate following T-cell activation.
4. Dohrman, A. et al. Cellular FLIP long form augments caspase activity and death of T cells through heterodimerization with and activation of caspase-8. J. Immunol. 175, 311–318 (2005).
5. Yeh, W. C. et al. Requirement for Casper (c-FLIP) in regulation of death receptor-induced apoptosis and embryonic development. Immunity 12, 633–642 (2000).
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