Mizuta Mitsuhiko, Nakajima Hiroo, Mizuta Naruhiko, Kitamura Yoshihiro, Nakajima Yasufumi, Hashimoto Soshi, Matsuyama Hiroki, Shime Nobuaki, Amaya Fumimasa, Koh Hidefumi, Ishizaka Akitoshi, Magae Junji, Tanuma Sei-ich, Hashimoto Satoru
Department of Anesthesiology and Intensive Care, Kyoto Prefectural University of Medicine, 465 Kajiicho, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, Japan.
Biol Pharm Bull. 2008 Mar;31(3):386-90. doi: 10.1248/bpb.31.386.
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.
肺泡上皮细胞死亡在急性肺损伤的进展中起关键作用。我们已证明急性肺损伤时肺泡上皮细胞上Fas表达上调,以及炎症细胞分泌可溶性Fas配体。在此我们表明,脂多糖刺激的人单核细胞系THP-1释放Fas配体,且脂多糖刺激的THP-1细胞的条件培养基可诱导人肺腺癌细胞系A549凋亡。半胱天冬酶-3和-8的激活与凋亡相关。通过特异性小干扰RNA对A549细胞中的Fas进行基因靶向会损害活化的THP-1条件培养基诱导的凋亡,而对THP-1细胞中的Fas配体进行基因靶向则会损害脂多糖刺激细胞产生的条件培养基的凋亡诱导活性。这些结果表明,单核细胞释放的Fas配体在急性肺损伤发展过程中通过Fas依赖性凋亡机制导致肺泡上皮细胞死亡。