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Synaptotagmin-Like Proteins Control Formation of a Single Apical Membrane Domain in Epithelial Cells

The formation of epithelial tissues requires both the generation of apical-basal polarity and the co-ordination of this polarity between neighboring cells to form a central lumen. During de novo lumen formation, vectorial membrane transport contributes to formation of a singular apical membrane, res...

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Detalles Bibliográficos
Autores principales: Gálvez-Santisteban, Manuel, Rodriguez-Fraticelli, Alejo E., Bryant, David M., Vergarajauregui, Silvia, Yasuda, Takao, Bañón-Rodríguez, Inmaculada, Bernascone, Ilenia, Datta, Anirban, Spivak, Natalie, Young, Kitty, Slim, Christiaan L., Brakeman, Paul R., Fukuda, Mitsunori, Mostov, Keith E., Martín-Belmonte, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433678/
https://www.ncbi.nlm.nih.gov/pubmed/22820376
http://dx.doi.org/10.1038/ncb2541
Descripción
Sumario:The formation of epithelial tissues requires both the generation of apical-basal polarity and the co-ordination of this polarity between neighboring cells to form a central lumen. During de novo lumen formation, vectorial membrane transport contributes to formation of a singular apical membrane, resulting in contribution of each cell to only a single lumen. Here, from a functional screen for genes required for 3D epithelial architecture we identify key roles for Synaptotagmin-like proteins 2-a and 4-a (Slp2-a/4-a) in generation of a single apical surface per cell. Slp2-a localizes to the luminal membrane in a PI(4,5)P(2)-dependent manner, where it targets Rab27-loaded vesicles to initiate a single lumen. Vesicle tethering and fusion is controlled by Slp4-a, in conjunction with Rab27/Rab3/Rab8 and the SNARE Syntaxin-3. Together, Slp2-a/4-a co-ordinate the spatiotemporal organization of vectorial apical transport to ensure only a single apical surface, and thus formation of a single lumen, occurs per cell.