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.

Highlights

  • Sphingolipids (SLs) are relevant lipid components of eukaryotic cells

  • Madin-Darby canine kidney (MDCK) morphological changes were evaluated by differential interference contrast (DIC) microscopy

  • Confluent MDCK cells cultured in isotonic medium displayed an elongated fibroblast-like phenotype (Fig. 1A-a), whereas, when cultured in hypertonic medium for 48 h, they acquired a more packed cobblestone-like morphology, typical of differentiated epithelial cells (Fig. 1A-b)

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Summary

Introduction

Sphingolipids (SLs) are relevant lipid components of eukaryotic cells. Besides regulating various cellular processes, SLs provide the structural framework for plasma membrane organization. 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 demonstrated that under hypertonic conditions, Madin-Darby canine kidney (MDCK) cells acquire a differentiated phenotype with changes in SL metabolism. We found that SM synthesis mediated by SM synthase 1 is involved in hypertonicityinduced formation of mature AJs, necessary for correct epithelial cell differentiation.

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