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.

Sci. STKE, 28 June 2005
Vol. 2005, Issue 290, p. tw240
[DOI: 10.1126/stke.2902005tw240]


REACTIVE OXYGEN SPECIES Protective at Low Concentrations?

Reactive oxygen species (ROS), which are produced as normal by-products of aerobic metabolism, have been implicated in aging and in the pathogenesis of cancer, cardiovascular diseases, and neurodegenerative disorders. However, antioxidants have not shown consistent benefits against cardiovascular disease, and evidence that ROS may also play a protective role has begun to emerge. Tang et al. found that, in various cultured cells, low to moderate concentrations of H2O2 inhibited the enzymatic activity of Src family tyrosine kinases (SFKs) as well as their phosphorylation on a conserved tyrosine residue that is phosphorylated in the activated form. The in vitro catalytic activity of two recombinant SFKs, however, was not sensitive to H2O2. Although the tyrosine phosphorylation of all SFK-bound substrates immunoprecipitated from cell lysates was inhibited after brief exposure to H2O2 (10 minutes), the phosphorylation of a subset of proteins recovered after longer exposures (60 minutes). Immunofluorescence analysis of human umbilical vein endothelial cells (HUVECs) indicated that H2O2 inactivated SFKs at focal adhesions and the plasma membrane but that prolonged exposure led to the activation of cytoplasmic SFKs. Pretreatment of HUVECs with H2O2 inhibited the activation of extracellular signal-regulated kinase (ERK) by platelet-derived growth factor (PDGF) as well as thrombin- or tumor necrosis factor-α (TNF-α)-dependent expression of vascular cell adhesion molecule-1. Thus, the authors suggest that low concentrations of ROS may protect endothelial cells from inflammatory responses to cytokines and that this protective action is mediated through a rapid, but indirect, inactivation of SFKs.

H. Tang, Q. Hao, S. A. Rutherford, B. Low, Z. J. Zhao, Inactivation of Src family tyrosine kinases by reactive oxygen species in vivo. J. Biol. Chem. 280, 23918-23925 (2005). [Abstract] [Full Text]

Citation: Protective at Low Concentrations? Sci. STKE 2005, tw240 (2005).

To Advertise     Find Products

Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882