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细胞骨架调节机制:细胞外基质对主动脉内皮细胞蛋白带4.1的调节作用

Mechanisms of cytoskeletal regulation: modulation of aortic endothelial cell protein band 4.1 by the extracellular matrix.

作者信息

Leto T L, Pratt B M, Madri J A

出版信息

J Cell Physiol. 1986 Jun;127(3):423-31. doi: 10.1002/jcp.1041270311.

Abstract

The bovine aortic endothelial cell (BAEC) cytoskeleton is a complex structure modulated by many stimuli including release from contact inhibition and various components of the extracellular matrix (ECM). Transduction of information from the ECM to the cell nucleus proceeds via several complex pathways including the cytoskeleton. We have demonstrated the presence of an immunoreactive isoform of the human erythrocyte cytoskeletal protein band 4.1 (4.1) in BAEC. BAEC 4.1 is similar in molecular weight to the erythroid protein by immunoblot analyses and produces a similar pattern of cysteine specific cleavage products consistent with a cluster of cysteine residues previously described in the erythroid molecule. We have also examined the effects of defined ECM proteins on the distributions of cultured BAEC 4.1 and actin filaments (AF) at confluency and following release from contact inhibition. The distribution of 4.1 in BAEC on a plasma fibronectin substrate is complex, having partial codistribution with cytoplasmic AF and a unique perinuclear staining. In contrast, on a collagen type I/III substrate, 4.1 is localized, in part, to peripheral areas of cell-cell contact distinct from the dense peripheral band staining of AF. During migration on this substrate, 4.1 had a filamentous distribution having partial codistribution with AF. Indirect immunofluorescence staining of cross-sections of bovine calf aortae revealed a cortical staining pattern in the aortic endothelial cells with staining noted on the luminal and basolateral aspects of the cells. These data suggest that, in endothelial cells, protein 4.1 is a cortical membrane protein which may function to link actin filaments to other skeletal proteins such as spectrin. These findings also suggest an active role for protein 4.1 in cytoskeletal reorganization events which can occur in response to external stimuli, such as the extracellular matrix or contact with other cells.

摘要

牛主动脉内皮细胞(BAEC)的细胞骨架是一个复杂的结构,受到许多刺激的调节,包括接触抑制的解除和细胞外基质(ECM)的各种成分。信息从ECM传递到细胞核通过包括细胞骨架在内的几条复杂途径进行。我们已经证实在BAEC中存在人红细胞细胞骨架蛋白带4.1(4.1)的免疫反应性同工型。通过免疫印迹分析,BAEC 4.1的分子量与红细胞蛋白相似,并产生类似的半胱氨酸特异性裂解产物模式,这与先前在红细胞分子中描述的半胱氨酸残基簇一致。我们还研究了特定ECM蛋白对汇合时以及接触抑制解除后培养的BAEC 4.1和肌动蛋白丝(AF)分布的影响。在血浆纤连蛋白底物上,BAEC中4.1的分布很复杂,部分与细胞质AF共分布,并具有独特的核周染色。相比之下,在I/III型胶原底物上,4.1部分定位于细胞-细胞接触的周边区域,与AF的致密周边带染色不同。在该底物上迁移期间,4.1呈丝状分布,部分与AF共分布。牛犊主动脉横截面的间接免疫荧光染色显示主动脉内皮细胞中有皮质染色模式,在细胞的腔面和基底外侧均有染色。这些数据表明,在内皮细胞中,蛋白4.1是一种皮质膜蛋白,其可能起到将肌动蛋白丝与其他骨架蛋白(如血影蛋白)连接的作用。这些发现还表明蛋白4.1在细胞骨架重组事件中发挥积极作用,这些事件可能响应外部刺激(如细胞外基质或与其他细胞的接触)而发生。

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