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首页> 外文期刊>Cell motility and the cytoskeleton >Immunocytochemical localization of polyamines during attachment and spreading of retinal pigment epithelial and intestinal epithelial cells.
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Immunocytochemical localization of polyamines during attachment and spreading of retinal pigment epithelial and intestinal epithelial cells.

机译:视网膜色素上皮和肠上皮细胞附着和扩散过程中多胺的免疫细胞化学定位。

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In order to form and maintain a protective barrier for photoreceptors, the retinal pigment epithelium relies on integrin signaling and related pathways to form adhesion complexes, undergo cell spreading, and establish a confluent cellular monolayer. Polyamines are multifunctional polycations that are essential for cell attachment and spreading, although their exact mechanisms of action are as yet unclear. We report new immunocytochemical evidence suggesting that in the cells of retinal pigment epithelium and also the intestinal epithelium, polyamines are present in a population of intracellular vesicles that appear transiently during initial stages of cell spreading. In newly attached cells with minimal spreading, the vesicles are seen near the nucleus, whereas in more highly spread cells, the vesicles are localized to the plasma membrane, near, but not precisely co-localized with an enzyme marker for adhesion complexes, focal adhesion kinase. We also observe pronounced nuclear staining in newly attached cells that have not spread, whereas this staining is decreased in cells that have spread. Nuclear staining has been previously reported in other cell types and has been attributed to DNA binding of polyamines, which is known to stabilize chromatin structure. We hypothesize that the appearance of polyamine vesicles near focal adhesions of cells undergoing attachment and spreading may reflect the mechanism by which polyamine pools are targeted to appropriate interaction sites necessary for the assembly of adhesion complexes. Alternatively, the vesicles could represent the mechanism by which polyamines are removed from the nucleus and possibly released from the cell. Cell Motil. Cytoskeleton 58:269-280, 2004.
机译:为了形成并维持对感光体的保护性屏障,视网膜色素上皮依赖整联蛋白信号传导和相关途径来形成粘附复合物,经历细胞扩散并建立汇合的细胞单层。多胺是多功能的聚阳离子,对于细胞附着和扩散至关重要,尽管它们的确切作用机理尚不清楚。我们报告新的免疫细胞化学证据表明,在视网膜色素上皮细胞以及肠上皮细胞中,多胺存在于细胞内囊泡群体中,在细胞扩散的初始阶段会短暂出现。在扩散最小的新附着细胞中,囊泡可见于细胞核附近,而在扩散程度更高的细胞中,囊泡位于质膜附近,但与酶标记物(但不精确地共定位于黏附复合物,粘着斑)激酶。我们还观察到尚未扩散的新附着细胞明显的核染色,而在扩散的细胞中这种染色减少。先前已经在其他细胞类型中报道了核染色,并且核染色归因于多胺的DNA结合,已知该结合可稳定染色质结构。我们假设,多胺囊泡在细胞附着和散布的局灶性粘连附近的出现可能反映了将多胺池靶向粘附复合物组装所必需的适当相互作用位点的机制。或者,囊泡可以代表多胺从细胞核中去除并可能从细胞中释放的机制。细胞动力。细胞骨架58:269-280,2004。

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