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Three mechanisms control E-cadherin localization to the zonula adherens.
Woichansky, Innokenty; Beretta, Carlo Antonio; Berns, Nicola; Riechmann, Veit.
Afiliação
  • Woichansky I; Department of Cell and Molecular Biology and Division of Signaling and Functional Genomics at the German Cancer Research Center (DKFZ), Medical Faculty Mannheim, Heidelberg University, Ludolf-Krehl-Strasse 13-17, D-68167 Mannheim, Germany.
  • Beretta CA; Heidelberg University, COS and Nikon Imaging Center at the University of Heidelberg, Bioquant, D-69120 Heidelberg, Germany.
  • Berns N; Excellenzcluster CellNetworks, University of Heidelberg, D-69120 Heidelberg, Germany.
  • Riechmann V; Department of Cell and Molecular Biology and Division of Signaling and Functional Genomics at the German Cancer Research Center (DKFZ), Medical Faculty Mannheim, Heidelberg University, Ludolf-Krehl-Strasse 13-17, D-68167 Mannheim, Germany.
Nat Commun ; 7: 10834, 2016 Mar 10.
Article em En | MEDLINE | ID: mdl-26960923
ABSTRACT
E-cadherin localization to the zonula adherens is fundamental for epithelial differentiation but the mechanisms controlling localization are unclear. Using the Drosophila follicular epithelium we genetically dissect E-cadherin transport in an in vivo model. We distinguish three mechanisms mediating E-cadherin accumulation at the zonula adherens. Two membrane trafficking pathways deliver newly synthesized E-cadherin to the plasma membrane. One is Rab11 dependent and targets E-cadherin directly to the zonula adherens, while the other transports E-cadherin to the lateral membrane. Lateral E-cadherin reaches the zonula adherens by endocytosis and targeted recycling. We show that this pathway is dependent on RabX1, which provides a functional link between early and recycling endosomes. Moreover, we show that lateral E-cadherin is transported to the zonula adherens by an apically directed flow within the plasma membrane. Differential activation of these pathways could facilitate cell shape changes during morphogenesis, while their misregulation compromises cell adhesion and tissue architecture in differentiated epithelia.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caderinas / Membrana Celular / Proteínas rab de Ligação ao GTP / Proteínas rab5 de Ligação ao GTP / Junções Aderentes / Transporte Proteico / Proteínas de Drosophila / Células Epiteliais Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caderinas / Membrana Celular / Proteínas rab de Ligação ao GTP / Proteínas rab5 de Ligação ao GTP / Junções Aderentes / Transporte Proteico / Proteínas de Drosophila / Células Epiteliais Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article