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Basolateral sorting and transcytosis define the Cu+-regulated translocation of ATP7B to the bile canaliculus
Author(s) -
Vasiliki Lalioti,
Ramón PeiróPastor,
Manuela Pérez-Gómez,
Yo Tsuchiya,
Angeles Muñoz,
Teresa Villalba,
Carlos M. Sánchez,
Ignacio V. Sandoval
Publication year - 2016
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.184663
Subject(s) - biology , transcytosis , bone canaliculus , microbiology and biotechnology , sorting , chromosomal translocation , endocytosis , biochemistry , anatomy , cell , gene , computer science , programming language
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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