Nuclear biochemical changes that are characteristic of apoptosis and can be induced by a variety of cytotoxic stimuli are traditionally associated with the executive or late stages of this form of cell death. The long-term objective of this proposal is to advance our understanding of nuclear participation in the initiative or early stages of apoptosis. The main hypothesis to be studied is that DNA-damaging agents stimulate apoptosis by imparting changes at the nuclear level, resulting in the release of factors into the cytosol, which target mitochondria and stimulate the release of cytochrome c. Because of the apparent ability of Hsp27 to exert its anti-apoptotic effect against a variety of stimuli, including DNA-damaging agents, at the level of cytochrome c release, the mechanism regulating the cytoprotective potential of this protein is a complementary focus of this proposal.
The specific aims are: 1) To characterize the ability of nuclei to stimulate established mitochondrial changes typical of apoptosis in response to DNA-damaging agents and the ability of Bcl-2/Bcl-XL to mitigate this effect; 2) To determine the mechanism(s) regulating the ability of Hsp27 to prevent apoptosomal caspase activation by blocking cytochrome c release. Completion of these studies will help clarify the ability of nuclear events, induced by DNA damage, to evoke mitochondrial changes characteristic of apoptosis and the mechanism responsible for Hsp27-mediated cytoprotection at the mitochondrial level.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32CA083273-03
Application #
6663251
Study Section
Special Emphasis Panel (ZRG1-SSS-3 (02))
Program Officer
Lohrey, Nancy
Project Start
2002-03-29
Project End
2003-12-30
Budget Start
2003-03-29
Budget End
2003-12-30
Support Year
3
Fiscal Year
2003
Total Cost
$31,986
Indirect Cost
Name
Karolinska Institute
Department
Type
DUNS #
350582235
City
Stockholm
State
Country
Sweden
Zip Code
171 7-7
Tamm, Christoffer; Robertson, John D; Sleeper, Eric et al. (2004) Differential regulation of the mitochondrial and death receptor pathways in neural stem cells. Eur J Neurosci 19:2613-21
Robertson, John D; Gogvadze, Vladimir; Kropotov, Andrey et al. (2004) Processed caspase-2 can induce mitochondria-mediated apoptosis independently of its enzymatic activity. EMBO Rep 5:643-8
Gogvadze, Vladimir; Robertson, John D; Enoksson, Mari et al. (2004) Mitochondrial cytochrome c release may occur by volume-dependent mechanisms not involving permeability transition. Biochem J 378:213-7
Ott, Martin; Robertson, John D; Gogvadze, Vladimir et al. (2002) Cytochrome c release from mitochondria proceeds by a two-step process. Proc Natl Acad Sci U S A 99:1259-63
Robertson, J D; Fadeel, B; Zhivotovsky, B et al. (2002) 'Centennial' Nobel Conference on apoptosis and human disease. Cell Death Differ 9:468-75
Robertson, John D; Orrenius, Sten (2002) Role of mitochondria in toxic cell death. Toxicology 181-182:491-6
Robertson, John D; Enoksson, Mari; Suomela, Minna et al. (2002) Caspase-2 acts upstream of mitochondria to promote cytochrome c release during etoposide-induced apoptosis. J Biol Chem 277:29803-9