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Sphingomyelin metabolism is involved in the differentiation of MDCK cells induced by environmental hypertonicity

机译:鞘磷脂代谢参与环境高渗诱导的MDCK细胞分化

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摘要

Sphingolipids (SLs) are relevant lipid components of eukaryotic cells. Besides regulating various cellular processes, SLs provide the structural framework for plasma membrane organization. Particularly, SM is associated with detergent-resistant microdomains. We have previously shown that the adherens junction (AJ) complex, the relevant cell-cell adhesion structure involved in cell differentiation and tissue organization, is located in an SM-rich membrane lipid domain. We have also demonstrated that under hypertonic conditions, Madin-Darby canine kidney (MDCK) cells acquire a differentiated phenotype with changes in SL metabolism. For these reasons, we decided to evaluate whether SM metabolism is involved in the acquisition of the differentiated phenotype of MDCK cells. We found that SM synthesis mediated by SM synthase 1 is involved in hypertonicity-induced formation of mature AJs, necessary for correct epithelial cell differentiation. Inhibition of SM synthesis impaired the acquisition of mature AJs, evoking a disintegration-like process reflected by the dissipation of E-cadherin and β- and α-catenins from the AJ complex. As a consequence, MDCK cells did not develop the hypertonicity-induced differentiated epithelial cell phenotype.
机译:鞘脂(SLs)是真核细胞的相关脂质成分。除了调节各种细胞过程外,SL还提供质膜组织的结构框架。特别地,SM与耐洗涤剂的微区有关。先前我们已经表明,粘附连接(AJ)复合体(参与细胞分化和组织组织的相关细胞-细胞粘附结构)位于富含SM的膜脂质结构域中。我们还证明,在高渗条件下,Madin-Darby犬肾(MDCK)细胞会随着SL代谢的变化而获得分化的表型。由于这些原因,我们决定评估SM代谢是否参与MDCK细胞分化表型的获得。我们发现由SM合酶1介导的SM合成参与高渗诱导的成熟AJ的形成,这对于正确的上皮细胞分化是必需的。抑制SM合成会损害成熟AJ的获得,从而引起类似崩解的过程,这是由E-钙黏着蛋白和β-和α-连环蛋白从AJ络合物中的消散反映出来的。结果,MDCK细胞不发展高渗诱导的分化的上皮细胞表型。

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