[ICE family proteins]
- PMID: 9309141
[ICE family proteins]
Abstract
Interleukin-1 beta-converting enzyme (ICE) was originally identified as a novel type of cysteine protease responsible for the conversion of percursor interleukin-1 beta to mature form. ICE is also a mammalian homologue of the Caenorhabitis elegans cell death protein Ced-3. Several ICE/ced-3 family proteases have been isolated and were recently renamed "Caspase." The overexpression of those proteases induces apoptosis. Moreover, it has been reported that several types of stimuli-induced apoptosis are equally inhibited by caspase-specific inhibitors, indicating that caspase proteases are common mediators of apoptosis. During induction of apoptosis, caspase proteases are thought to be sequentially activated and cleave several cellular proteins essential for cell growth.
Similar articles
-
[Involvement of ICE/CED 3 family proteases in antitumor agent-induced apoptosis].Gan To Kagaku Ryoho. 1997 Jan;24(2):211-5. Gan To Kagaku Ryoho. 1997. PMID: 9030233 Japanese.
-
Peptidyl beta-homo-aspartals (3-amino-4-carboxybutyraldehydes): new specific inhibitors of caspases.Biopolymers. 1999;51(1):109-18. doi: 10.1002/(SICI)1097-0282(1999)51:1<109::AID-BIP12>3.0.CO;2-S. Biopolymers. 1999. PMID: 10380358
-
Requirement of an ICE/CED-3 protease for Fas/APO-1-mediated apoptosis.Nature. 1995 May 4;375(6526):81-3. doi: 10.1038/375081a0. Nature. 1995. PMID: 7536901
-
Execution mechanisms of programmed cell death by caspase (ICE/CED-3) family proteases.Heart Vessels. 1997;Suppl 12:66-70. Heart Vessels. 1997. PMID: 9476547 Review.
-
ICE/CED3-like proteases as therapeutic targets for the control of inappropriate apoptosis.Nat Biotechnol. 1996 Mar;14(3):297-301. doi: 10.1038/nbt0396-297. Nat Biotechnol. 1996. PMID: 9630889 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources