Miao J Y, Araki S, Kaji K, Hayashi H
Sugashima Marine Biological Laboratory, School of Science, Nagoya University Toba, Mie, Japan.
Biochem Biophys Res Commun. 1997 Apr 7;233(1):182-6. doi: 10.1006/bbrc.1997.6422.
To clarify the signal transduction in vascular endothelial cells (VEC) apoptosis induced by deprivation of FGF and serum, we investigated the function of integrin beta4 by using the monoclonal antibody (mAb) of this integrin. We added anti-beta 4 integrin mAb at the concentration of 5 microg/ml to the cells deprived of FGF and serum, apoptosis of these cells were completely inhibited 24 h after the treatment. Furthermore we plated the cells onto untreated bacterial culture plates on which the cells cannot adhere and spread in MCDB medium without FGF and serum; however, when anti-beta 4 integrin mAb was present at 5 microg/ml in the seeding medium, the cells rapidly adhered and spread. Our results first demonstrated that integrin beta4 participated in apoptotic signaling in VEC, and our findings indicate that hemidesmosome structures and keratin filament system might be important in regulation of apoptotic signaling.
为阐明因成纤维细胞生长因子(FGF)和血清缺乏所诱导的血管内皮细胞(VEC)凋亡中的信号转导,我们通过使用该整合素的单克隆抗体(mAb)来研究整合素β4的功能。我们将浓度为5微克/毫升的抗β4整合素单克隆抗体添加到缺乏FGF和血清的细胞中,处理24小时后这些细胞的凋亡被完全抑制。此外,我们将细胞接种到未经处理的细菌培养板上,在不含FGF和血清的MCDB培养基中细胞无法在其上黏附与铺展;然而,当接种培养基中存在浓度为5微克/毫升的抗β4整合素单克隆抗体时,细胞迅速黏附并铺展。我们的结果首次证明整合素β4参与了血管内皮细胞的凋亡信号传导,并且我们的研究结果表明半桥粒结构和角蛋白丝系统在凋亡信号传导的调节中可能很重要。