Marushige Y, Marushige K
Department of Pathology, Michigan State University, East Lansing 48824, USA.
Anticancer Res. 1995 Mar-Apr;15(2):267-72.
Chromatin condensation during apoptosis induced by TGF beta 1 in T24 glioma and 476-16 trigeminal neurinoma (Schwannoma) cells was examined and compared with that occurring during mitosis. Apoptotic (round-up) cells were selectively detached from the culture surface by a mechanical shock. Their histones were analysed in comparison with those obtained from TGF beta 1-treated cells remaining attached to the culture surface, from control cells not treated with TGF beta 1 and from metaphase cells. While mitosis-specific hyperphosphorylation of histones H1 and phosphorylation of histone H3 was not observed in apoptotic cells, apoptotic chromatin lacked ubiquitinated histone H2A (histone uH2A) as did metaphase chromosomes. The cellular level of free ubiquitin and the overall pattern of ubiquitin-conjugated proteins were, however, found to remain unaltered in apoptotic cells, suggesting that the ubiquitin conjugating machinery for histone H2A may be specifically perturbed during the chromatin condensation occurring in apoptosis.
研究了转化生长因子β1(TGFβ1)诱导T24胶质瘤细胞和476 - 16三叉神经鞘瘤(施万细胞瘤)细胞凋亡过程中的染色质凝聚,并与有丝分裂过程中的染色质凝聚进行了比较。通过机械冲击将凋亡(变圆)细胞从培养表面选择性分离。将其组蛋白与从仍附着于培养表面的TGFβ1处理细胞、未用TGFβ1处理的对照细胞以及中期细胞中获得的组蛋白进行分析比较。虽然在凋亡细胞中未观察到组蛋白H1的有丝分裂特异性过度磷酸化和组蛋白H3的磷酸化,但凋亡染色质与中期染色体一样缺乏泛素化组蛋白H2A(组蛋白uH2A)。然而,发现凋亡细胞中游离泛素的细胞水平和泛素缀合蛋白的总体模式保持不变,这表明在凋亡过程中发生的染色质凝聚期间,组蛋白H2A的泛素缀合机制可能受到特异性干扰。