## Abstract Transforming growth factor‐β1 (TGF‐β1) is crucially involved in the fibrotic events characterizing interstitial lung diseases (ILDs), as well as in the airway remodeling process typical of asthma. Within such a context, the aim of our study was to investigate, in primary cultures of nor
Effects of hydrogen peroxide on MAPK activation, IL-8 production and cell viability in primary cultures of human bronchial epithelial cells
✍ Scribed by Girolamo Pelaia; Giovanni Cuda; Alessandro Vatrella; Luca Gallelli; Donatella Fratto; Vincenza Gioffrè; Bruno D'Agostino; Mario Caputi; Rosario Maselli; Francesco Rossi; Francesco S. Costanzo; Serafino A. Marsico
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 269 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The airway epithelium is continuously exposed to inhaled oxidants, including airborne pollutants and cigarette smoke, which can exert harmful proinflammatory and cytotoxic effects. Therefore, the aim of our study was to investigate, in primary cultures of human bronchial epithelial cells (HBEC), the signal transduction pathways activated by increasing concentrations (0.25, 0.5, and 1 mM) of hydrogen peroxide (H~2~O~2~), as well as their effects on IL‐8 production and cell viability. The reported results show that H~2~O~2~ elicited, in a concentration‐dependent fashion, a remarkable increase in phosphorylation‐dependent activation of mitogen‐activated protein kinases (MAPKs), associated with a significant induction of IL‐8 synthesis and a dramatically enhanced cell death. Pre‐treatment of HBEC with MAPK inhibitors was able to significantly inhibit the effects of H~2~O~2~ on IL‐8 secretion, and to effectively prevent cell death. Therefore, these findings suggest that MAPKs play a key role as molecular transducers of the airway epithelial injury triggered by oxidative stress, as well as potential pharmacologic targets for indirect antioxidant intervention. © 2004 Wiley‐Liss, Inc.
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