Nishimura S, Hirakawa-Chung K Y, Yashiro M, Inoue T, Matsuoka T, Fujihara T, Murahashi K, Sawada T, Nakata B, Jikihara I, Takagi H, Sowa M
First Department of Surgery, Osaka City University Medical School, 1-5-7 Asahimachi, Abeno-ku, Osaka 545, Japan.
Int J Oncol. 1998 Apr;12(4):847-51. doi: 10.3892/ijo.12.4.847.
In vitro morphologic change of mesothelial cells was observed following the addition of serum-free conditioned medium (SF-CM) from peritoneal dissemination cell line OCUM-2MD3. The same morphologic change of mesothelial cells was observed following the addition of 10 ng/ml TGF-beta1, but not following the addition of b-FGF, IGF-I, VEGF or PDGF-AA. In the in vivo study, mesothelial cells of mice treated with SF-CM from OCUM-2MD3 and TGF- beta1 were separated from one another, resulting in exposure of the submesothelial connective tissue. The molecular size of the mesothelial morphology changing activity was estimated by running the SF-CM from OCUM-2MD3 through a gel filtration column TSK-gel G2000SW. The mesothelial morphology changing activity was recognized at positions equivalent of Mr 6, 500-30,000. 25 kDa TGF-beta1 was detected in the active fraction from the TSK-gel G2000SW column and the SF-CM of OCUM-2MD3 by Western blotting using a monoclonal antibody against TGF-beta1. These findings suggest that TGF-beta1 produced by gastric cancer cells changes the morphology of mesothelial cells and may thus be closely associated with peritoneal dissemination.
添加来自腹膜播散细胞系OCUM - 2MD3的无血清条件培养基(SF - CM)后,观察到间皮细胞的体外形态学变化。添加10 ng/ml转化生长因子β1(TGF - β1)后观察到间皮细胞出现相同的形态学变化,但添加碱性成纤维细胞生长因子(b - FGF)、胰岛素样生长因子I(IGF - I)、血管内皮生长因子(VEGF)或血小板衍生生长因子AA(PDGF - AA)后未观察到该变化。在体内研究中,用来自OCUM - 2MD3的SF - CM和TGF - β1处理的小鼠间皮细胞彼此分离,导致间皮下结缔组织暴露。通过将来自OCUM - 2MD3的SF - CM通过凝胶过滤柱TSK - gel G2000SW来估计间皮形态改变活性的分子大小。在相当于Mr 6,500 - 30,000的位置识别出间皮形态改变活性。通过使用抗TGF - β1单克隆抗体进行蛋白质印迹法,在来自TSK - gel G2000SW柱的活性级分和OCUM - 2MD3的SF - CM中检测到25 kDa的TGF - β1。这些发现表明,胃癌细胞产生的TGF - β1改变了间皮细胞的形态,因此可能与腹膜播散密切相关。