Bcl-2-family proteins play a key role in the control of apoptosis. In particular, gene targeting studies in mice have shown that Bax and Bak (and by analogy, perhaps Bok) are critical effectors; in the absence of these proteins, cells show deficiencies in many forms of apoptosis. Our focus is on how these Bcl-2-family proteins regulate mitochondrial outer membrane permeabilization (MOMP), a primary event in many cell death pathways. MOMP leads to the translocation of cytochrome c and other apoptotic trigger proteins from the mitochondria! inner membrane space into the cytoplasm; these proteins in turn regulate caspase activation and the execution phase of apoptosis. However, even if caspases are inactive or absent, MOMP nevertheless appears to doom most cells to die, through initiating a loss of key mitochondrial functions as well as the generation of reactive oxygen species. Thus, the regulation and mechanism of this process are of critical importance. Here we propose studies that will help elucidate the roles of Bcl-2-family proteins in MOMP. We will use both cell-free systems, to tease apart the mechanisms of action of these proteins, and whole-cell and in vivo approaches, which will extend these investigations to a more physiological context. There are three principal subgroups of the Bcl-2 family: """"""""BH1-4"""""""" proteins, which are anti-apoptotic; """"""""BH1-3"""""""" proteins, which include the pro-apoptotic family members Bax, Bak and Bok, and the """"""""BH3-only"""""""" proteins, which are also pro-apoptotic. The BH3-only proteins are more numerous, are activated specifically through transcriptional and post-translational mechanisms in the context of different cellular stresses, and appear to regulate the other two subfamilies.
Our aims, which address each category of the Bcl-2 family in turn, are first, to explore the mechanisms through which the BH3-only proteins regulate the activation of Bax-type proteins; second, to investigate the mechanism of membrane permeabilization by Bax-type proteins; and third, to understand how Bcl-xL, a member of the BH1-4 category, can both prevent MOMP and also reseal the MOM after MOMP has occurred. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM062289-08
Application #
7486163
Study Section
Cancer Molecular Pathobiology Study Section (CAMP)
Program Officer
Zatz, Marion M
Project Start
2001-03-01
Project End
2010-08-31
Budget Start
2008-09-01
Budget End
2010-08-31
Support Year
8
Fiscal Year
2008
Total Cost
$359,929
Indirect Cost
Name
La Jolla Institute
Department
Type
DUNS #
603880287
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Kushnareva, Y; Seong, Y; Andreyev, A Y et al. (2016) Mitochondrial dysfunction in an Opa1(Q285STOP) mouse model of dominant optic atrophy results from Opa1 haploinsufficiency. Cell Death Dis 7:e2309
Gillies, Laura A; Du, Han; Peters, Bjoern et al. (2015) Visual and functional demonstration of growing Bax-induced pores in mitochondrial outer membranes. Mol Biol Cell 26:339-49
Volkmann, N; Marassi, F M; Newmeyer, D D et al. (2014) The rheostat in the membrane: BCL-2 family proteins and apoptosis. Cell Death Differ 21:206-15
Kushnareva, Yulia; Andreyev, Alexander Y; Kuwana, Tomomi et al. (2012) Bax activation initiates the assembly of a multimeric catalyst that facilitates Bax pore formation in mitochondrial outer membranes. PLoS Biol 10:e1001394
Lartigue, Lydia; Kushnareva, Yulia; Seong, Youngmo et al. (2009) Caspase-independent mitochondrial cell death results from loss of respiration, not cytotoxic protein release. Mol Biol Cell 20:4871-84
Yamaguchi, Ryuji; Lartigue, Lydia; Perkins, Guy et al. (2008) Opa1-mediated cristae opening is Bax/Bak and BH3 dependent, required for apoptosis, and independent of Bak oligomerization. Mol Cell 31:557-69
Yamaguchi, R; Andreyev, A; Murphy, A N et al. (2007) Mitochondria frozen with trehalose retain a number of biological functions and preserve outer membrane integrity. Cell Death Differ 14:616-24
Bonzon, Christine; Bouchier-Hayes, Lisa; Pagliari, Lisa J et al. (2006) Caspase-2-induced apoptosis requires bid cleavage: a physiological role for bid in heat shock-induced death. Mol Biol Cell 17:2150-7
Kuwana, Tomomi; Bouchier-Hayes, Lisa; Chipuk, Jerry E et al. (2005) BH3 domains of BH3-only proteins differentially regulate Bax-mediated mitochondrial membrane permeabilization both directly and indirectly. Mol Cell 17:525-35
Kuwana, Tomomi; Mackey, Mason R; Perkins, Guy et al. (2002) Bid, Bax, and lipids cooperate to form supramolecular openings in the outer mitochondrial membrane. Cell 111:331-42