Alterations in the prooxidant and antioxidant status of human leukemic T-lymphocyte MOLT4 cells treated with potassium chromate

The involvement of reactive oxygen species in chromate-induced genotoxicity has been postulated. Because intracellular antioxidants help in eliminating the reactive species of oxygen, we have investigated both the prooxidant and antioxidant status of human leukemic T-lymphocyte MOLT4 cells exposed to nontoxic levels of chromium(VI) in culture. The cells treated with 0 200 M potassium chromate in a salts/glucose medium for 2 h were found to contain significantly lower levels of both small molecular weight and macromolecular antioxidants. In particular, the levels of glutathione and ascorbate were found to decrease with increased doses of chromate exposure in a dose-dependent manner. As little as 10 M chromate was found to decrease these small molecular weight antioxidants significantly (p<0.01). The macromolecular antioxidants, such as glutathione peroxidase, catalase, glutathione reductase, glucose-6-phosphate dehydrogenase and superoxide dismutase were also significantly (p<0.01) decreased by exposing the cells to as little as 10 M chromate. Concomitantly there was a dose-dependent increase in intracellular H₂O₂ accumulation in cells exposed to chromium(VI). These results indicate that chromate-induced genotoxicity may be due, at least in part, to decreased levels of intracellular antioxidants in conjunction with an increased production of the reactive oxygen species.     

TIMAP,a novel CAAX box protein regulated by TGF-beta1 and expressed in endothelial cells

Representational difference analysis ofthe glomerular endothelial cell response to transforming growthfactor-1 (TGF-1) revealed a novel gene, TIMAP (TGF--inhibitedmembrane-associated protein), which contains 10 exons and maps to humanchromosome 20.q11.22. By Northern blot, TIMAP mRNA is highly expressedin all cultured endothelial and hematopoietic cells. The frequency ofthe TIMAP SAGE tag is much greater in endothelial cell SAGE databasesthan in nonendothelial cells. Immunofluorescence studies of rat tissuesshow that anti-TIMAP antibodies localize to vascular endothelium.TGF-1 represses TIMAP through a protein synthesis- and histonedeacetylase-dependent process. The TIMAP protein contains five ankyrinrepeats, a protein phosphatase-1 (PP1)-interacting domain, aCOOH-terminal CAAX box, a domain arrangement similar to that of MYPT3,and a PP1 inhibitor. A green fluorescent protein-TIMAP fusion proteinlocalized to the plasma membrane in a CAAX box-dependent fashion.Hence, TIMAP is a novel gene highly expressed in endothelial andhematopoietic cells and regulated by TGF-1. On the basis of itsdomain structure, TIMAP may serve a signaling function, potentiallythrough interaction with PP1.