| Literature DB >> 18310897 |
Mitsuhiko Mizuta1, Hiroo Nakajima, Naruhiko Mizuta, Yoshihiro Kitamura, Yasufumi Nakajima, Soshi Hashimoto, Hiroki Matsuyama, Nobuaki Shime, Fumimasa Amaya, Hidefumi Koh, Akitoshi Ishizaka, Junji Magae, Sei-ich Tanuma, Satoru Hashimoto.
Abstract
Alveolar epithelial cell death plays a crucial role in the progression of acute lung injury. We have demonstrated up-regulation of Fas expression on alveolar epithelial cells, and soluble Fas ligand secretion from inflammatory cells upon acute lung injury. Here we show that the lipopolysaccharide-stimulated human monocyte cell line THP-1 releases Fas ligand, and that conditioned medium from lipopolysaccharide-stimulated THP-1 cells induces apoptosis of the human pulmonary adenocarcinoma cell line A549. Activation of caspase-3 and -8 is associated with the apoptosis. Gene targeting on Fas in A549 cells by specific small interfering RNA impairs apoptosis induced by conditioned medium from activated THP-1, while that on Fas ligand in THP-1 cells impairs the apoptosis-inducing activity of the conditioned medium produced by lipopolysaccharide-stimulated cells. These results suggest that Fas ligand released by monocytes causes alveolar epithelial cell death through a Fas-dependent apoptotic mechanism in the development of acute lung injury.Entities:
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Year: 2008 PMID: 18310897 DOI: 10.1248/bpb.31.386
Source DB: PubMed Journal: Biol Pharm Bull ISSN: 0918-6158 Impact factor: 2.233