Basolateral sorting and transcytosis define the Cu+-regulated translocation of ATP7B to the bile canaliculus

J Cell Sci. 2016 Jun 1;129(11):2190-201. doi: 10.1242/jcs.184663. Epub 2016 Mar 31.

Abstract

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(.)

Keywords: ATP7B; Bile canaliculus; Copper; TGN; Trafficking; Transcytosis.

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Bile Canaliculi / drug effects
  • Bile Canaliculi / metabolism*
  • Brefeldin A / pharmacology
  • Cation Transport Proteins / metabolism*
  • Cell Compartmentation / drug effects
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Copper / pharmacology*
  • Copper-Transporting ATPases
  • Guanine Nucleotide Exchange Factors / metabolism
  • Hep G2 Cells
  • Humans
  • Hydrazones / pharmacology
  • Lysosomes / drug effects
  • Lysosomes / metabolism
  • Macrolides / pharmacology
  • Microtubules / drug effects
  • Microtubules / metabolism
  • Protein Transport / drug effects
  • Rats
  • Secretory Vesicles / drug effects
  • Secretory Vesicles / metabolism
  • Transcytosis / drug effects*
  • trans-Golgi Network / drug effects
  • trans-Golgi Network / metabolism

Substances

  • Atp7a protein, mouse
  • Cation Transport Proteins
  • Guanine Nucleotide Exchange Factors
  • Hydrazones
  • Macrolides
  • N'-(3,4-dihydroxybenzylidene)-3-hydroxy-2-naphthahydrazide
  • Brefeldin A
  • Copper
  • bafilomycin A1
  • Adenosine Triphosphatases
  • Copper-Transporting ATPases