Dexamethasone protects RAW264.7 macrophages from growth arrest and apoptosis induced by H2O2 through alteration of gene expression patterns and inhibition of nuclear factor-kappa B (NF-κB) activity
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
Author(s)
Detail(s)
Original language | English |
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Pages (from-to) | 16-28 |
Journal / Publication | Toxicology |
Volume | 236 |
Issue number | 1-2 |
Publication status | Published - 1 Jul 2007 |
Link(s)
Abstract
In this study, the effect of dexamethasone, a synthetic glucocorticoid, on H2O2 stimulated murine RAW264.7 macrophages was investigated. It was found that dexamethasone protected the cells from apoptosis induced by H2O2. A cDNA microarray, which consists of 1000 genes selected from a mouse clone set provided from NIA, was used to study the gene expression profiles involved in the protective effect. Our data show that dexamethasone exerts the anti-apoptosis function by changing the expression patterns of many genes involved inhibiting the up-regulation of apoptosis promoting genes and the down-regulation of cell cycle stimulating genes as well as keeping the up-regulation of cell survival related genes. Our study also revealed that dexamethasone protects RAW264.7 macrophages from H2O2 induced apoptosis through blocking nuclear factor-kappa B (NF-κB) activity. © 2007 Elsevier Ireland Ltd. All rights reserved.
Research Area(s)
- Dexamethasone, Gene expression, Hydrogen peroxide, NF-κB activity, RAW264.7 macrophages
Citation Format(s)
Dexamethasone protects RAW264.7 macrophages from growth arrest and apoptosis induced by H2O2 through alteration of gene expression patterns and inhibition of nuclear factor-kappa B (NF-κB) activity. / Fong, Chi-Chun; Zhang, Yaou; Zhang, Qi et al.
In: Toxicology, Vol. 236, No. 1-2, 01.07.2007, p. 16-28.
In: Toxicology, Vol. 236, No. 1-2, 01.07.2007, p. 16-28.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review