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首页> 外文期刊>Journal of cell biology >Insoluble γ-Tubulin–Containing Structures Are Anchored to the Apical Network of Intermediate Filaments in Polarized Caco-2 Epithelial Cells
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Insoluble γ-Tubulin–Containing Structures Are Anchored to the Apical Network of Intermediate Filaments in Polarized Caco-2 Epithelial Cells

机译:含不溶性γ-微管蛋白的结构锚定在极化的Caco-2上皮细胞的中间细丝的顶端网络中

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We have previously shown that a thin (~1 μm) layer of intermediate filaments located beneath the apical membrane of a variety of simple epithelial cells participates in the organization of apical microfilaments and microtubules. Here, I confirmed the apical distribution of γ-tubulin–containing structures (potential microtubule-organizing centers) in CACO-2 cells and demonstrated perfect colocalization of centrosomes and nearly 50% of noncentrosomal γ-tubulin with apical intermediate filaments, but not with apical F-actin. Furthermore, the antisense-oligonucleotide–mediated downregulation of cytokeratin 19, using two different antisense sequences, was more efficient than anticytoskeletal agents to delocalize centrosomes. Electron microscopy colocalization suggests that binding occurs at the outer boundary of the pericentriolar material. Type I cytokeratins 18 and 19 present in these cells specifically coimmunoprecipitated in multi-protein fragments of the cytoskeleton with γ-tubulin. The size and shape of the fragments, visualized at the EM level, indicate that physical trapping is an unlikely explanation for this result. Drastic changes in the extraction protocol did not affect coimmunoprecipitation. These results from three independent techniques, indicate that insoluble γ-tubulin–containing structures are attached to apical intermediate filaments.
机译:我们先前已经证明,位于各种简单上皮细胞的顶膜下方的中间丝细丝(〜1μm)层参与了顶丝微丝和微管的组织。在这里,我确认了CACO-2细胞中含有γ-微管蛋白的结构的顶端分布(潜在的微管组织中心),并证明了中心体和近50%的非中心体γ-微管蛋白与顶端中间细丝的完美共定位,但没有顶端F-肌动蛋白。此外,使用两个不同的反义序列,由反义寡核苷酸介导的细胞角蛋白19的下调比抗细胞骨架剂更有效地使中心体离域。电子显微镜共定位表明结合发生在中心小周材料的外边界。这些细胞中存在的I型细胞角蛋白18和19与γ-微管蛋白特异性共免疫沉淀在细胞骨架的多蛋白片段中。在EM级别可视化的碎片大小和形状表明,物理诱捕不太可能解释该结果。提取方案的剧烈变化不会影响免疫共沉淀。这些来自三种独立技术的结果表明,不溶性含γ-微管蛋白的结构附着在顶端中间丝上。

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