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鸡砂囊平滑肌细胞中的肌动蛋白同工型区室

Actin isoform compartments in chicken gizzard smooth muscle cells.

作者信息

North A J, Gimona M, Lando Z, Small J V

机构信息

Institute of Molecular Biology, Austrian Academy of Sciences, Salzburg.

出版信息

J Cell Sci. 1994 Mar;107 ( Pt 3):445-55. doi: 10.1242/jcs.107.3.445.

Abstract

Differentiated smooth muscle cells typically contain a mixture of muscle (alpha and gamma) and cytoplasmic (beta and gamma) actin isoforms. Of the cytoplasmic actins the beta-isoform is the more dominant, making up from 10% to 30% of the total actin complement. Employing an antibody raised against the N-terminal peptide specific to beta-actin, which labels only the beta-isoform on two-dimensional gel immunoblots, we have shown that this isoform has a restricted localisation in smooth muscle. Using double-label immunofluorescence and immunoelectron microscopy of ultrathin sections of chicken gizzard, beta-actin was localised in the dense bodies and in longitudinal channels linking consecutive dense bodies that were also occupied by desmin. It was additionally found in the membrane-associated dense plaques, but was excluded from the actomyosin-containing regions of the contractile apparatus. Taken together with earlier results these findings identify a cytoskeletal compartment containing intermediate filaments, cytoplasmic actin and the actin cross-linking protein filamin. Using an antibody specific only for muscle actin, labelling was found generally around the myosin filaments of the contractile apparatus, but was absent from the core of the dense bodies that contained beta-actin. Thus, if dense bodies act as dual-purpose anchorage sites, for the cytoskeletal actin and the contractile actin, the thin filaments of the contractile apparatus must be anchored at the periphery of the dense bodies. A model of the structural organisation of the cell is presented and the possible roles of the cytoskeleton are discussed.

摘要

分化的平滑肌细胞通常含有肌肉型(α和γ)和胞质型(β和γ)肌动蛋白异构体的混合物。在胞质肌动蛋白中,β异构体更为主要,占肌动蛋白总量的10%至30%。利用针对β-肌动蛋白特异的N端肽段产生的抗体,该抗体在二维凝胶免疫印迹上仅标记β异构体,我们已表明这种异构体在平滑肌中有局限的定位。通过对鸡砂囊超薄切片进行双重标记免疫荧光和免疫电子显微镜观察,β-肌动蛋白定位于致密体以及连接连续致密体的纵向通道中,这些通道中也有结蛋白。此外,在与膜相关的致密斑中也发现了β-肌动蛋白,但收缩装置中含肌动球蛋白的区域没有。结合早期结果,这些发现确定了一个包含中间丝、胞质肌动蛋白和肌动蛋白交联蛋白细丝蛋白的细胞骨架区室。使用仅对肌肉肌动蛋白特异的抗体,在收缩装置的肌球蛋白丝周围普遍发现有标记,但含β-肌动蛋白的致密体核心没有标记。因此,如果致密体作为细胞骨架肌动蛋白和收缩性肌动蛋白的两用锚定位点,那么收缩装置的细肌丝必须锚定在致密体的周边。本文提出了细胞结构组织的模型,并讨论了细胞骨架的可能作用。

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