Mrp2/Abcc2 transport activity is stimulated by protein kinase Calpha in a baculo virus co-expression system

Life Sci. 2005 Jun 17;77(5):539-50. doi: 10.1016/j.lfs.2004.10.071. Epub 2005 Feb 23.


Cholestatic and choleretic effect are well known for protein kinase C activator and inhibitor, respectively. However, post-translational regulation, especially the effect of phosphorylation status of the biliary transporters on their intrinsic transport activity has not been fully understood. In this study, effect of phosphorylation on the transport activity of Mrp2, a biliary organic anion transporter, was examined in membrane vesicles isolated from Sf9 cells co-expressing excess amount of protein kinase Calpha (PKCalpha). Mrp2-mediated transport activity was enhanced to three-fold by co-expressing PKCalpha. At the same time, phosphorylation of Mrp2 was also detected. The Km and Vmax values for the transport of [3H]estradiol-17beta-D-glucuronide exhibited a 1.5-fold decrease and a 1.9-fold increase, respectively. Probenecid (100 microM) and benzylpenicillin (1 mM), both are activator of Mrp2, did not stimulated the transport activity of phosphorylated Mrp2. On the other hand, transport activity was further stimulated by Estron-3-sulfate and taurocholic acid. Similar mechanism that occurred in the presence of probenecid and benzylpenicillin, but different from that occurred in the presence of Estron-3-sulfate and taurocholic acid seems to be involved in the stimulation. Considering the discrepancy between the previous in vivo inhibitory effect of PKC activators and our in vitro stimulatory effect of PKCalpha on Mrp2 transport activity, direct modulation of Mrp2-transport activity may be minor if any under in vivo condition.

MeSH terms

  • ATP-Binding Cassette Transporters / genetics
  • ATP-Binding Cassette Transporters / metabolism*
  • Animals
  • Baculoviridae / enzymology*
  • Baculoviridae / genetics
  • Bile Canaliculi / drug effects
  • Bile Canaliculi / enzymology*
  • Biological Transport
  • Cell Membrane Structures / drug effects
  • Cell Membrane Structures / metabolism
  • Cloning, Molecular
  • Insecta / enzymology
  • Insecta / virology
  • Phosphorylation
  • Protein Kinase C / genetics
  • Protein Kinase C / metabolism*
  • Protein Kinase C-alpha
  • Rats
  • Rats, Sprague-Dawley
  • Substrate Specificity
  • Transport Vesicles / drug effects
  • Transport Vesicles / enzymology*


  • ATP-Binding Cassette Transporters
  • Abcc2 protein, rat
  • Protein Kinase C
  • Protein Kinase C-alpha