Trielli M O, Andreassen P R, Lacroix F B, Margolis R L
Institut de Biologie Structurale Jean-Pierre Ebel (CEA-CNRS), Grenoble, France.
J Cell Biol. 1996 Nov;135(3):689-700. doi: 10.1083/jcb.135.3.689.
Taxol (paclitaxel) induces a microtubule hyperassembled state, and effectively blocks cells in mitosis. Here we report that Taxol also induces a stable late-G1 block in nontransformed REF-52 and WI-38 mammalian fibroblast cells, but not in T antigen-transformed cells of the same parental lineage. G1 arrest is characterized by partially dephosphorylated pRb, and inactive cdk2 kinase. Nontransformed cells recover normally from Taxol arrest. In contrast, T antigen transformed cells continue inappropriately past both G1 and G2-M in the presence of Taxol, and undergo a rapid death upon release. These results demonstrate a microtubule sensitive step in G1 regulation of nontransformed fibroblast cells. Also, Taxol selectively induces death of transformed cells, possibly because they slip the Taxol-dependent G1 arrest, as well as G2/M arrest, which are both specific to nontransformed cells.
紫杉醇(paclitaxel)可诱导微管超组装状态,并有效阻断细胞有丝分裂。在此我们报告,紫杉醇还能在未转化的REF-52和WI-38哺乳动物成纤维细胞中诱导稳定的G1晚期阻滞,但在相同亲代谱系的T抗原转化细胞中则不会。G1期停滞的特征是部分去磷酸化的pRb和无活性的cdk2激酶。未转化的细胞能从紫杉醇阻滞中正常恢复。相比之下,T抗原转化细胞在紫杉醇存在的情况下会不恰当地越过G1期和G2-M期,并在解除阻滞时迅速死亡。这些结果证明了未转化成纤维细胞G1期调控中存在一个微管敏感步骤。此外,紫杉醇选择性地诱导转化细胞死亡,可能是因为它们逃避了依赖紫杉醇的G1期阻滞以及G2/M期阻滞,而这两种阻滞都是未转化细胞所特有的。