Bursch W, Oberhammer F, Jirtle R L, Askari M, Sedivy R, Grasl-Kraupp B, Purchio A F, Schulte-Hermann R
Institute for Tumorbiology-Cancer Research, University of Vienna, Wien, Austria.
Br J Cancer. 1993 Mar;67(3):531-6. doi: 10.1038/bjc.1993.98.
Cell death by apoptosis is a major determinant of growth of normal tissues and tumours. The present study aimed to elucidate signal factors involved in its regulation. Epithelial cells in control liver, during regression of cyproterone acetate induced liver hyperplasia, in liver (pre)neoplasia and in uterus undergoing apoptosis in vivo show immunostaining for transforming growth factor beta 1 (TGF-beta 1) as detected by anti-pre(266-278) TGF-beta 1 antibodies. Positive immunostaining is also seen in a few intact cells of hyperplastic, regressing liver apparently preparing for apoptosis, but is virtually not found in hepatocytes of normal or growing liver nor in cells undergoing death by necrosis. Recombinant latency associated protein (rLAP, dimer of the pro-region non-covalently associated with the mature region) complex and mature TGF-beta 1 induce apoptosis in isolated hepatocytes cultured in vitro. These findings suggest an involvement of TGF-beta 1 in the induction of apoptosis in certain epithelia in vivo.
细胞凋亡引起的细胞死亡是正常组织和肿瘤生长的主要决定因素。本研究旨在阐明参与其调控的信号因子。在醋酸环丙孕酮诱导的肝增生消退过程中、在肝脏(癌)前期以及在体内发生凋亡的子宫中,对照肝脏的上皮细胞经抗前体(266 - 278)转化生长因子β1(TGF-β1)抗体检测显示有TGF-β1免疫染色。在增生、消退的肝脏中一些显然正准备凋亡的完整细胞中也可见阳性免疫染色,但在正常或生长中的肝脏的肝细胞中以及在因坏死而死亡的细胞中几乎未发现。重组潜伏相关蛋白(rLAP,前体区域与成熟区域非共价结合的二聚体)复合物和成熟的TGF-β1可在体外培养的分离肝细胞中诱导凋亡。这些发现提示TGF-β1参与体内某些上皮细胞凋亡的诱导过程。