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- Publisher Website: 10.1016/j.cell.2005.03.016
- Scopus: eid_2-s2.0-21144451097
- PMID: 15907471
- WOS: WOS:000229331200014
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Article: Specific ablation of the apoptotic functions of cytochrome c reveals a differential requirement for cytochrome c and Apaf-1 in apoptosis
Title | Specific ablation of the apoptotic functions of cytochrome c reveals a differential requirement for cytochrome c and Apaf-1 in apoptosis |
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Authors | |
Issue Date | 2005 |
Citation | Cell, 2005, v. 121, n. 4, p. 579-591 How to Cite? |
Abstract | As components of the apoptosome, a caspase-activating complex, cytochrome c (Cyt c) and Apaf-1 are thought to play critical roles during apoptosis. Due to the obligate function of Cyt c in electron transport, its requirement for apoptosis in animals has been difficult to establish. We generated "knockin" mice expressing a mutant Cyt c (KA allele), which retains normal electron transfer function but fails to activate Apaf-1. Most KA/KA mice displayed embryonic or perinatal lethality caused by defects in the central nervous system, and surviving mice exhibited impaired lymphocyte homeostasis. Although fibroblasts from the KA/KA mice were resistant to apoptosis, their thymocytes were markedly more sensitive to death stimuli than Apaf-1 -/- thymocytes. Upon treatment with γ irradiation, procaspases were efficiently activated in apoptotic KA/KA thymocytes, but Apaf-1 oligomerization was not observed. These studies indicate the existence of a Cyt c- and apoptosome-independent but Apaf-1-dependent mechanism(s) for caspase activation. Copyright ©2005 by Elsevier Inc. |
Persistent Identifier | http://hdl.handle.net/10722/292190 |
ISSN | 2023 Impact Factor: 45.5 2023 SCImago Journal Rankings: 24.342 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Hao, Zhenyue | - |
dc.contributor.author | Duncan, Gordon S. | - |
dc.contributor.author | Chang, Chia Che | - |
dc.contributor.author | Elia, Andrew | - |
dc.contributor.author | Fang, Min | - |
dc.contributor.author | Wakeham, Andrew | - |
dc.contributor.author | Okada, Hitoshi | - |
dc.contributor.author | Calzascia, Thomas | - |
dc.contributor.author | Jang, Yingju | - |
dc.contributor.author | You-Ten, Annick | - |
dc.contributor.author | Yeh, Wen Chen | - |
dc.contributor.author | Ohashi, Pamela | - |
dc.contributor.author | Wang, Xiaodong | - |
dc.contributor.author | Mak, Tak W. | - |
dc.date.accessioned | 2020-11-17T14:55:57Z | - |
dc.date.available | 2020-11-17T14:55:57Z | - |
dc.date.issued | 2005 | - |
dc.identifier.citation | Cell, 2005, v. 121, n. 4, p. 579-591 | - |
dc.identifier.issn | 0092-8674 | - |
dc.identifier.uri | http://hdl.handle.net/10722/292190 | - |
dc.description.abstract | As components of the apoptosome, a caspase-activating complex, cytochrome c (Cyt c) and Apaf-1 are thought to play critical roles during apoptosis. Due to the obligate function of Cyt c in electron transport, its requirement for apoptosis in animals has been difficult to establish. We generated "knockin" mice expressing a mutant Cyt c (KA allele), which retains normal electron transfer function but fails to activate Apaf-1. Most KA/KA mice displayed embryonic or perinatal lethality caused by defects in the central nervous system, and surviving mice exhibited impaired lymphocyte homeostasis. Although fibroblasts from the KA/KA mice were resistant to apoptosis, their thymocytes were markedly more sensitive to death stimuli than Apaf-1 -/- thymocytes. Upon treatment with γ irradiation, procaspases were efficiently activated in apoptotic KA/KA thymocytes, but Apaf-1 oligomerization was not observed. These studies indicate the existence of a Cyt c- and apoptosome-independent but Apaf-1-dependent mechanism(s) for caspase activation. Copyright ©2005 by Elsevier Inc. | - |
dc.language | eng | - |
dc.relation.ispartof | Cell | - |
dc.title | Specific ablation of the apoptotic functions of cytochrome c reveals a differential requirement for cytochrome c and Apaf-1 in apoptosis | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1016/j.cell.2005.03.016 | - |
dc.identifier.pmid | 15907471 | - |
dc.identifier.scopus | eid_2-s2.0-21144451097 | - |
dc.identifier.volume | 121 | - |
dc.identifier.issue | 4 | - |
dc.identifier.spage | 579 | - |
dc.identifier.epage | 591 | - |
dc.identifier.isi | WOS:000229331200014 | - |
dc.identifier.f1000 | 1026105 | - |
dc.identifier.issnl | 0092-8674 | - |