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Physiological extracellular electrical signals guide and orient the polarity of gut epithelial cells

机译:生理学细胞外电信号指导和定向肠道上皮细胞的极性

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摘要

Apical-basal polarity in epithelial cells is a fundamental process in the morphogenesis of many tissues. But how epithelial cells become oriented with functionally specialized luminal and serosal facing membranes is not understood fully. Cell-cell and cell-substrate contacts induce the asymmetric distribution of Na+/K+-ATPase pumps on basal membrane and are essential for apical-basal polarity formation. Inhibition of the Na+/K+-ATPase pump abolished apical formation completely. But it is unclear how this pump regulated the apical polarity. We discovered that the transepithelial potential difference (TEP) which is dependent on the basal Na+/K+-ATPase distribution acts as an essential coordinating signal for apical membrane formation through Ror2/ERK1/2/LKB1 signaling. A similar concept applies to all other ion-transporting epithelial and endothelial tissues and this raises the possibility of regulating the TEP as a therapeutic intervention for disorders in which epithelial function is compromised by faulty electrical signaling.
机译:上皮细胞的顶基极极性是许多组织形态发生的基本过程。但是尚不完全了解上皮细胞如何通过功能性的腔壁和浆膜面向膜定向。细胞-细胞和细胞-底物的接触引起基底膜上Na + / K + -ATPase泵的不对称分布,这对顶基-极性的形成至关重要。 Na + / K + -ATPase泵的抑制作用完全消除了根尖的形成。但尚不清楚该泵如何调节顶端极性。我们发现,依赖于基础Na + / K + -ATPase分布的上皮电位差(TEP)作为通过Ror2形成顶膜的重要协调信号/ ERK1 / 2 / LKB1信令。类似的概念适用于所有其他离子运输的上皮和内皮组织,这增加了调节TEP作为治疗性干预措施的可能性,以治疗由于电信号故障而损害上皮功能的疾病。

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