Unknown

Dataset Information

0

Opa1-mediated cristae opening is Bax/Bak and BH3 dependent, required for apoptosis, and independent of Bak oligomerization.


ABSTRACT: Controversy surrounds the role and mechanism of mitochondrial cristae remodeling in apoptosis. Here we show that the proapoptotic BH3-only proteins Bid and Bim induced full cytochrome c release but only a subtle alteration of crista junctions, which involved the disassembly of Opa1 complexes. Both mitochondrial outer membrane permeabilization (MOMP) and crista junction opening (CJO) were caspase independent and required a functional BH3 domain and Bax/Bak. However, MOMP and CJO were experimentally separable. Pharmacological blockade of MOMP did not prevent Opa1 disassembly and CJO; moreover, expression of a disassembly-resistant mutant Opa1 (Q297V) blocked cytochrome c release and apoptosis but not Bax activation. Thus, apoptosis requires a subtle form of Opa1-dependent crista remodeling that is induced by BH3-only proteins and Bax/Bak but independent of MOMP.

SUBMITTER: Yamaguchi R 

PROVIDER: S-EPMC2636708 | biostudies-literature | 2008 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Opa1-mediated cristae opening is Bax/Bak and BH3 dependent, required for apoptosis, and independent of Bak oligomerization.

Yamaguchi Ryuji R   Lartigue Lydia L   Perkins Guy G   Scott Ray T RT   Dixit Amruta A   Kushnareva Yulia Y   Kuwana Tomomi T   Ellisman Mark H MH   Newmeyer Donald D DD  

Molecular cell 20080807 4


Controversy surrounds the role and mechanism of mitochondrial cristae remodeling in apoptosis. Here we show that the proapoptotic BH3-only proteins Bid and Bim induced full cytochrome c release but only a subtle alteration of crista junctions, which involved the disassembly of Opa1 complexes. Both mitochondrial outer membrane permeabilization (MOMP) and crista junction opening (CJO) were caspase independent and required a functional BH3 domain and Bax/Bak. However, MOMP and CJO were experimental  ...[more]

Similar Datasets

| S-EPMC2681411 | biostudies-literature
| S-EPMC6888900 | biostudies-literature
| S-EPMC2417179 | biostudies-literature
| S-EPMC3373601 | biostudies-literature
| S-EPMC3135403 | biostudies-literature
| S-EPMC3832543 | biostudies-literature
| S-EPMC5841295 | biostudies-literature
| S-EPMC3618047 | biostudies-literature
| S-EPMC4650538 | biostudies-literature
| S-EPMC3277102 | biostudies-literature