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鞘磷脂代谢参与环境高渗诱导的MDCK细胞分化。

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

作者信息

Favale Nicolás Octavio, Santacreu Bruno Jaime, Pescio Lucila Gisele, Marquez Maria Gabriela, Sterin-Speziale Norma Beatriz

机构信息

Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Argentina IQUIFIB-LANAIS-PROEM-CONICET, Ciudad Autónoma de Buenos Aires, Argentina.

IQUIFIB-LANAIS-PROEM-CONICET, Ciudad Autónoma de Buenos Aires, Argentina Instituto de Investigaciones en Ciencias de la Salud Humana (IICSHUM), Universidad Nacional de La Rioja , La Rioja, Argentina.

出版信息

J Lipid Res. 2015 Apr;56(4):786-800. doi: 10.1194/jlr.M050781. Epub 2015 Feb 10.

DOI:10.1194/jlr.M050781
PMID:25670801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4373737/
Abstract

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.

摘要

鞘脂(SLs)是真核细胞中重要的脂质成分。除了调节各种细胞过程外,鞘脂还为质膜组织提供结构框架。特别是,鞘磷脂(SM)与抗去污剂微区相关。我们之前已经表明,黏附连接(AJ)复合体,即参与细胞分化和组织形成的相关细胞间黏附结构,位于富含SM的膜脂结构域中。我们还证明,在高渗条件下,Madin-Darby犬肾(MDCK)细胞会通过鞘脂代谢的变化获得分化表型。基于这些原因,我们决定评估鞘磷脂代谢是否参与MDCK细胞分化表型的获得。我们发现,由鞘磷脂合酶1介导的鞘磷脂合成参与了高渗诱导的成熟AJs的形成,这是正确的上皮细胞分化所必需的。抑制鞘磷脂合成会损害成熟AJs的获得,引发一种类似解体的过程,表现为E-钙黏蛋白以及β-连环蛋白和α-连环蛋白从AJ复合体中消散。结果,MDCK细胞没有形成高渗诱导的分化上皮细胞表型。

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