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PMID: 10770918 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Activation of the cytoplasmic c-Abl tyrosine kinase by reactive oxygen species.

The Journal of biological chemistry ·Vol. 275 ·No. 23 ·2000-06-09 ·Pages 17237-40

Sun X, Majumder P, Shioya H, Wu F, Kumar S, Weichselbaum R, Kharbanda S, Kufe D

Abstract

The ubiquitously expressed c-Abl protein tyrosine kinase localizes to both the nucleus and cytoplasm. The nuclear form of c-Abl is activated in the cellular response to genotoxic stress. Here we show that cytoplasmic c-Abl is activated by oxidative stress. The results also demonstrate that mitochondrial cytochrome c is released in the cellular response to H(2)O(2) and that this effect is mediated by a c-Abl-dependent mechanism. In concert with these results, we show that H(2)O(2)-induced apoptosis is attenuated in c-Abl-deficient cells. These findings demonstrate that cytoplasmic c-Abl is involved in the apoptotic response of cells to oxidative stress.

MeSH Terms
Acetylcysteine/pharmacology Animals COS Cells Cell Nucleus/enzymology Cells, Cultured Cytoplasm/enzymology Embryo, Mammalian Enzyme Activation/drug effects Fibroblasts/cytology,physiology Hydrogen Peroxide/pharmacology Mice Mice, Knockout Proto-Oncogene Proteins c-abl/deficiency,genetics,metabolism Reactive Oxygen Species/physiology
Chemicals
Reactive Oxygen Species Hydrogen Peroxide Proto-Oncogene Proteins c-abl Acetylcysteine
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Sun X
Dana-Farber Cancer Institute, Harvard Medical School, Boston Massachusetts 02115, USA.
Majumder P
Shioya H
Wu F
Kumar S
Weichselbaum R
Kharbanda S
Kufe D
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2000-06-09
Pages
17237-40
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA42802 · United States
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