Kupffer cells alter organic anion transport through multidrug resistance protein 2 in the post-cold ischemic rat liver

Hepatology. 2004 Apr;39(4):1099-109. doi: 10.1002/hep.20104.

Abstract

Although Kupffer cells (KCs) may play a crucial role in post-cold ischemic hepatocellular injury, their role in nonnecrotic graft dysfunction remains unknown. This study examined reveal the role of KC in post-cold ischemic liver grafts. Rat livers treated with or without liposome-encapsulated dichloromethylene diphosphonate, a KC-depleting reagent, were stored in University of Wisconsin (UW) solution at 4 degrees C for 8 to 24 hours and reperfused while monitoring biliary output and constituents. The ability of hepatocytes to excrete bile was assessed through laser-confocal microfluorography in situ. Cold ischemia-reperfused grafts decreased their bile output significantly at 8 hours without any notable cell injury. This event coincided with impaired excretion of glutathione and bilirubin-IXalpha (BR-IXalpha), suggesting delayed transport of these organic anions. We examined whether intracellular relocalization of multidrug resistance protein-2 (Mrp2) occurred. Kinetic analyses for biliary excretion of carboxyfluorescein, a fluoroprobe excreted through this transporter, revealed significant delay of dye excretion from hepatocytes into bile canaliculi. The KC-depleting treatment significantly attenuated this decline in biliary anion transport mediated through Mrp2 in the 8-hour cold ischemic grafts via redistribution of Mrp2 from the cytoplasm to the canalicular membrane. Furthermore, thromboxane A(2) (TXA(2)) synthase in KC appeared involved as blocking this enzyme improved 5-carboxyfluorescein excretion while cytoplasmic internalization of Mrp2 disappeared in the KC-depleting grafts. In conclusion, KC activation is an important determinant of nonnecrotic hepatocellular dysfunction, jeopardizing homeostasis of the detoxification capacity and organic anion metabolism of the post-cold ischemic grafts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP-Binding Cassette Transporters*
  • Animals
  • Bile / metabolism
  • Bilirubin / metabolism
  • Carrier Proteins / metabolism*
  • Cold Temperature
  • Cryopreservation*
  • Fluoresceins / pharmacokinetics
  • Glutathione / metabolism
  • Ischemia / metabolism*
  • Kupffer Cells / metabolism*
  • Liver / cytology
  • Liver / metabolism
  • Liver Transplantation
  • Male
  • Rats
  • Rats, Wistar
  • Thromboxanes / biosynthesis

Substances

  • ATP-Binding Cassette Transporters
  • Abcc2 protein, rat
  • Carrier Proteins
  • Fluoresceins
  • Thromboxanes
  • 4-carboxyfluorescein
  • Glutathione
  • Bilirubin