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从诺考达唑处理中释放后,活的PTK2细胞中有丝分裂微管的有核组装。

Nucleated assembly of mitotic microtubules in living PTK2 cells after release from nocodazole treatment.

作者信息

De Brabander M, Geuens G, De Mey J, Joniau M

出版信息

Cell Motil. 1981;1(4):469-83. doi: 10.1002/cm.970010407.

Abstract

The reassembly of microtubules is described in mitotic cells after release from nocodazole-induced block. The formation of microtubules was followed by light microscopic immunocytochemical staining using the PAP method, combined with toluidine blue staining of the chromatin. The light microscopic observations on whole cells were compared with ultrastructural observations on thin sections. This step is essential to ascertain complete destruction of microtubules during the nocodazole treatment and to correlate immunocytochemical staining with the presence of microtubules. Removal of nocodazole (10 or 1 micrograms/ml) after a sufficiently long incubation to induce a complete disappearance of microtubules resulted in the appearance of tubulin staining specifically associated with the centromeres and with one or two isolated points in the cytoplasm. Electron microscopy confirmed that the staining was due to the massive accumulation of small microtubules at the kinetochores and centrosomes. Kinetochore nucleation was seen only in association with condensed metaphase-stage chromosomes and not with the less-condensed prophase chromosomes. In a second type of experiment cells were allowed to enter mitosis in the presence of an incompletely active concentration of nocodazole (0.1 microgram/ml). The construction of the mitotic spindle was arrested; however, short microtubules were assembled at the kinetochores and centrosomes. These experiments demonstrate that in living mitotic PTK2 cells the kinetochores, as well as the centrosomes, exert a nucleating action on tubulin assembly. The further elongation of microtubules after removal of nocodazole was seen to occur preferentially along axes between the centrosomes and the kinetochores. This resulted in the construction of normal metaphases that evolved through anaphase and telophase. We have attempted to formulate a hypothesis that may explain the oriented assembly that seems to be essential in the construction of the spindle.

摘要

在从诺考达唑诱导的阻滞中释放后,有丝分裂细胞中微管的重新组装情况如下所述。微管的形成通过使用PAP法的光镜免疫细胞化学染色进行跟踪,并结合染色质的甲苯胺蓝染色。将对整个细胞的光镜观察结果与对薄片的超微结构观察结果进行比较。这一步骤对于确定诺考达唑处理期间微管的完全破坏以及将免疫细胞化学染色与微管的存在相关联至关重要。在经过足够长时间的孵育以诱导微管完全消失后,去除诺考达唑(10或1微克/毫升),导致出现与着丝粒以及细胞质中一两个孤立点特异性相关的微管蛋白染色。电子显微镜证实,这种染色是由于着丝粒和中心体处小微管的大量积累所致。仅在与浓缩的中期染色体相关联时才观察到着丝粒成核,而与浓缩程度较低的前期染色体无关。在另一类实验中,使细胞在不完全活性浓度的诺考达唑(0.1微克/毫升)存在下进入有丝分裂。有丝分裂纺锤体的构建被阻止;然而,短微管在着丝粒和中心体处组装。这些实验表明,在活的有丝分裂PTK2细胞中,着丝粒以及中心体对微管蛋白组装发挥成核作用。去除诺考达唑后微管的进一步伸长优先沿着中心体和着丝粒之间的轴发生。这导致构建出通过后期和末期演化的正常中期。我们试图提出一个假说,该假说可能解释在纺锤体构建中似乎至关重要的定向组装。

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