Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Connected to Death: The (Unexpurgated) Mitochondrial Pathway of Apoptosis
Diana Spierings,
Gavin McStay,
Maya Saleh,*
Cheryl Bender,
Jerry Chipuk,
Uli Maurer,
Douglas R. Green
Abstract:
The mitochondrial pathway of apoptosis in vertebrates is dependenton the process of mitochondrial outer membrane permeabilization(MOMP), which leads to the release of proteins from the mitochondrialintermembrane space into the cytosol. "Upstairs" of this eventare the Bcl-2 family proteins that regulate and mediate MOMP;"downstairs" is the activation of caspases that orchestratethe dismantling of the cell. In the Connections Map databaseat Science's Signal Transduction Knowledge Environment (STKE),the pathways that define the mitochondrial pathway of apotosisare illustrated, with the bulk of control occurring "upstairs"of MOMP.
La Jolla Institute for Allergy and Immunology, 10355 Science Center Drive, San Diego, CA 92121, USA.
* Present address: Department of Medicine, McGill University,687 Pine Avenue West, Montreal, Quebec H3A 1A1, Canada.
Present address: Department of Immunology, St. Jude Children'sResearch Hospital, 332 North Lauderdale, Memphis, TN 38105,USA.
To whom correspondence should be addressed. E-mail: dgreen5240{at}aol.com
The editors suggest the following Related Resources on Science sites:
In Science Magazine
INTRODUCTION TO SPECIAL ISSUE
L. Bryan Ray, Nancy R. Gough, and Elizabeth M. Adler (7 October 2005) Science310 (5745), 65.
[DOI: 10.1126/science.310.5745.65] |Summary »|PDF »
In Science Signaling
EDITORIAL GUIDES
Nancy R. Gough, Elizabeth M. Adler, and L. Bryan Ray (11 October 2005) Sci. STKE2005 (305), eg9.
[DOI: 10.1126/stke.3052005eg9] |Abstract »|Full Text »|PDF »
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Maintenance of the secondary structure of horse cytochrome c during the conversion process of monomers to oligomers by addition of ethanol.
S. Hirota, M. Ueda, Y. Hayashi, S. Nagao, H. Kamikubo, and M. Kataoka (2012)
J. Biochem.
152, 521-529
|Abstract »|Full Text »|PDF »
S. Mitsuhashi, H. Hatakeyama, M. Karahashi, T. Koumura, I. Nonaka, Y. K. Hayashi, S. Noguchi, R. B. Sher, Y. Nakagawa, G. Manfredi, et al. (2011)
Hum. Mol. Genet.
20, 3841-3851
|Abstract »|Full Text »|PDF »
The mechanism of neogambogic acid-induced apoptosis in human MCF-7 cells.
K. Wang, Y. Tang, M. Sun, B. Lu, H. Zhu, O. Ji, and Q. Shen (2011)
Acta Biochim Biophys Sin
43, 698-702
|Abstract »|Full Text »|PDF »
Overexpression of peroxisomal testis-specific 1 protein induces germ cell apoptosis and leads to infertility in male mice.
K. Kaczmarek, M. Studencka, A. Meinhardt, K. Wieczerzak, S. Thoms, W. Engel, and P. Grzmil (2011)
Mol. Biol. Cell
22, 1766-1779
|Abstract »|Full Text »|PDF »
Cytochrome c polymerization by successive domain swapping at the C-terminal helix.
S. Hirota, Y. Hattori, S. Nagao, M. Taketa, H. Komori, H. Kamikubo, Z. Wang, I. Takahashi, S. Negi, Y. Sugiura, et al. (2010)
PNAS
107, 12854-12859
|Abstract »|Full Text »|PDF »
Mitaplatin, a potent fusion of cisplatin and the orphan drug dichloroacetate.
p53 Mutant Human Glioma Cells Are Sensitive to UV-C-Induced Apoptosis Due to Impaired Cyclobutane Pyrimidine Dimer Removal.
L. F.Z. Batista, W. P. Roos, B. Kaina, and C. F.M. Menck (2009)
Mol. Cancer Res.
7, 237-246
|Abstract »|Full Text »|PDF »
Scythe Regulates Apoptosis-inducing Factor Stability during Endoplasmic Reticulum Stress-induced Apoptosis.
F. Desmots, H. R. Russell, D. Michel, and P. J. McKinnon (2008)
J. Biol. Chem.
283, 3264-3271
|Abstract »|Full Text »|PDF »
Gender-Related Differences in Apoptotic Pathways After Neonatal Cerebral Ischemia.
S. Renolleau, S. Fau, and C. Charriaut-Marlangue (2008)
Neuroscientist
14, 46-52
|Abstract »|PDF »
The mitochondrial respiratory chain is a modulator of apoptosis.
J. Q. Kwong, M. S. Henning, A. A. Starkov, and G. Manfredi (2007)
J. Cell Biol.
179, 1163-1177
|Abstract »|Full Text »|PDF »
Comparative Biophysical Characterization of p53 with the Pro-apoptotic BAK and the Anti-apoptotic BCL-xL.
B. Sot, S. M. V. Freund, and A. R. Fersht (2007)
J. Biol. Chem.
282, 29193-29200
|Abstract »|Full Text »|PDF »
XIAP Activity Dictates Apaf-1 Dependency for Caspase 9 Activation.
A. T. Ho, Q. H. Li, H. Okada, T. W. Mak, and E. Zacksenhaus (2007)
Mol. Cell. Biol.
27, 5673-5685
|Abstract »|Full Text »|PDF »
Identification and Characterization of Cannabinoids That Induce Cell Death through Mitochondrial Permeability Transition in Cannabis Leaf Cells.
S. Morimoto, Y. Tanaka, K. Sasaki, H. Tanaka, T. Fukamizu, Y. Shoyama, Y. Shoyama, and F. Taura (2007)
J. Biol. Chem.
282, 20739-20751
|Abstract »|Full Text »|PDF »
Caspase-9 regulates apoptosis/proliferation balance during metamorphic brain remodeling in Xenopus.
L. Coen, K. Le Blay, I. Rowe, and B. A. Demeneix (2007)
PNAS
104, 8502-8507
|Abstract »|Full Text »|PDF »
Autophagy occurs upstream or parallel to the apoptosome during histolytic cell death.
F. Akdemir, R. Farkas, P. Chen, G. Juhasz, L. Medved'ova, M. Sass, L. Wang, X. Wang, S. Chittaranjan, S. M. Gorski, et al. (2006)
Development
133, 1457-1465
|Abstract »|Full Text »|PDF »