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Basolateral sorting and transcytosis define the Cu+-regulated translocation of ATP7B to the bile canaliculus.
Lalioti, Vasiliki; Peiró, Ramón; Pérez-Berlanga, Manuela; Tsuchiya, Yo; Muñoz, Angeles; Villalba, Teresa; Sanchez, Carlos; Sandoval, Ignacio V.
Afiliación
  • Lalioti V; Department of Cell Biology and Immunology, Centro de Biología Molecular Severo Ochoa, Cantoblanco, Madrid 28049, Spain.
  • Peiró R; Department of Genomics and Massive Sequencing, Centro de Biología Molecular Severo Ochoa, Cantoblanco, Madrid 28049, Spain.
  • Pérez-Berlanga M; Department of Cell Biology and Immunology, Centro de Biología Molecular Severo Ochoa, Cantoblanco, Madrid 28049, Spain.
  • Tsuchiya Y; Department of Cell Biology and Immunology, Centro de Biología Molecular Severo Ochoa, Cantoblanco, Madrid 28049, Spain.
  • Muñoz A; Department of Optical and Confocal Microscopy, Centro de Biología Molecular Severo Ochoa, Cantoblanco, Madrid 28049, Spain.
  • Villalba T; Department of Optical and Confocal Microscopy, Centro de Biología Molecular Severo Ochoa, Cantoblanco, Madrid 28049, Spain.
  • Sanchez C; Department of Optical and Confocal Microscopy, Centro de Biología Molecular Severo Ochoa, Cantoblanco, Madrid 28049, Spain.
  • Sandoval IV; Department of Cell Biology and Immunology, Centro de Biología Molecular Severo Ochoa, Cantoblanco, Madrid 28049, Spain isandoval@cbm.csic.es.
J Cell Sci ; 129(11): 2190-201, 2016 06 01.
Article en En | MEDLINE | ID: mdl-27034138
The Cu(+) pump ATP7B plays an irreplaceable role in the elimination of excess Cu(+) by the hepatocyte into the bile. The trafficking and site of action of ATP7B are subjects of controversy. One current proposal is that an increase in intracellular Cu(+) results in the translocation of ATP7B to the lysosomes and excretion of excess Cu(+) through lysosomal-mediated exocytosis at the bile canaliculus. Here, we show that ATP7B is transported from the trans-Golgi network (TGN) to the bile canaliculus by basolateral sorting and endocytosis, and microtubule-mediated transcytosis through the subapical compartment. Trafficking ATP7B is not incorporated into lysosomes, and addition of Cu(+) does not cause relocalization of lysosomes and the appearance of lysosome markers in the bile canaliculus. Our data reveal the pathway of the Cu(+)-mediated transport of ATP7B from the TGN to the bile canaliculus and indicates that the bile canaliculus is the primary site of ATP7B action in the elimination of excess Cu(.)
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Canalículos Biliares / Adenosina Trifosfatasas / Cobre / Proteínas de Transporte de Catión / Transcitosis Límite: Animals / Humans Idioma: En Revista: J Cell Sci Año: 2016 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Canalículos Biliares / Adenosina Trifosfatasas / Cobre / Proteínas de Transporte de Catión / Transcitosis Límite: Animals / Humans Idioma: En Revista: J Cell Sci Año: 2016 Tipo del documento: Article País de afiliación: España
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