Title: Cd2+ versus Zn2+ uptake by the ZIP8 HCO3--dependent symporter: kinetics, electrogenicity and trafficking.

Authors: Liu, Zhiwei; Li, Hong; Soleimani, Manoocher; Girijashanker, Kuppuswami; Reed, Jodie M; He, Lei; Dalton, Timothy P; Nebert, Daniel W

Published In Biochem Biophys Res Commun, (2008 Jan 25)

Abstract: The mouse Slc39a8 gene encodes the ZIP8 transporter, which has been shown to be a divalent cation/HCO3- symporter. Using ZIP8 cRNA-injected Xenopus oocyte cultures, we show herein that: [a] ZIP8-mediated cadmium (Cd(2+)) and zinc (Zn(2+)) uptake have V(max) values of 1.8+/-0.08 and 1.0+/-0.08 pmol/oocyte/h, and K(m) values of 0.48+/-0.08 and 0.26+/-0.09 microM, respectively; [b] ZIP8-mediated Cd(2+) uptake is most inhibited by Zn(2+), second-best inhibited by Cu(2+), Pb(2+) and Hg(2+), and not inhibited by Mn(2+) or Fe(2+); and [c] electrogenicity studies demonstrate an influx of two HCO3- anions per one Cd(2+) (or one Zn(2+)) cation, i.e. electroneutral complexes. Using Madin-Darby canine kidney (MDCK) polarized epithelial cells retrovirally infected with ZIP8 cDNA and tagged with hemagglutinin at the C-terminus, we show that-similar to ZIP4-the ZIP8 eight-transmembrane protein is largely internalized during Zn(2+) homeostasis, but moves predominantly to the cell surface membrane (trafficking) under conditions of Zn(2+) depletion.

PubMed ID: 18037372

MeSH Terms: Animals; Cadmium/pharmacokinetics*; Cation Transport Proteins/metabolism*; Cell Line; Dogs; Ion Channel Gating/physiology*; Kidney/metabolism*; Protein Transport/physiology*; Zinc/pharmacokinetics*