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Contacts and cooperation between cells depend on the hormone ouabain

机译:细胞之间的接触与合作取决于哇巴因激素

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Cell adhesion is a crucial step in proliferation, differentiation, migration, apoptosis, and metastasis. In previous works we have shown that cell adhesion is modulated by ouabain, a highly specific inhibitor of Na+,K+-ATPase, recently found to be a hormone. In the present work we pursue the investigation of the effect of ouabain on a special type of cell-cell interaction: the rescue of ouabain-sensitive MDCK cells (W) by ouabain-resistant cells (R). In cultured monolayers of pure W cells, ouabain triggers the "P -> A mechanism" (from pump/adhesion) consisting of a cascade of phosphorylations that retrieves adhesion-associated molecules occludin and,6-catenin and results in detachment of the cell. When W cells are instead cocultured with R cells, the P -> A reaction is blocked, and W cells are rescued. Furthermore, in these R/W cocultures ouabain promotes cell-cell communication by means of gap junctions by specifically enhancing the expression of connexin 32 and addressing this molecule to the plasma membrane. Cluabain also promotes the internalization of the beta-subunit of the Na+,K+-ATPase. These observations open the possibility that the crucial processes mentioned at the beginning would be under the control of the hormone ouabain.
机译:细胞粘附是增殖,分化,迁移,凋亡和转移中的关键步骤。在以前的工作中,我们已经证明了细胞粘附是由哇巴因调节的,哇巴因是最近发现是激素的Na +,K + -ATPase的高度特异性抑制剂。在本工作中,我们继续研究哇巴因对特殊类型的细胞-细胞相互作用的影响:哇巴因抗性细胞(R)对哇巴因敏感的MDCK细胞(W)的拯救。在培养的纯W细胞单层细胞中,哇巴因会触发“ P-> A机制”(来自泵/粘附),由一连串的磷酸化组成,该磷酸化可回收与粘附相关的分子oclludin和6-catenin,并导致细胞脱离。当W细胞与R​​细胞共培养时,P-> A反应被阻断,W细胞得以拯救。此外,在这些R / W共培养物中,哇巴因通过特异性增强连接蛋白32的表达并将该分子定位于质膜上,通过间隙连接促进细胞间的通讯。克鲁巴因还促进Na +,K + -ATP酶的β-亚基的内在化。这些发现打开了开头提到的关键过程将在激素哇巴因控制下的可能性。

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