Ferroportin 1 is expressed basolaterally in rat kidney proximal tubule cells and iron excess increases its membrane trafficking

Natascha A. Wolff, Wei Liu, Robert A. Fenton, Wing Kee Lee, Frank Thévenod, Craig P. Smith

Research output: Contribution to journalArticlepeer-review

Abstract

Ferroportin 1 (FPN1) is an iron export protein expressed in liver and duodenum, as well as in reticuloendothelial macrophages. Previously, we have shown that divalent metal transporter 1 (DMT1) is expressed in late endosomes and lysosomes of the kidney proximal tubule (PT), the nephron segment responsible for the majority of solute reabsorption. We suggested that following receptor mediated endocytosis of transferrin filtered by the glomerulus, DMT1 exports iron liberated from transferrin into the cytosol. FPN1 is also expressed in the kidney yet its role remains obscure. As a first step towards determining the role of renal FPN1, we localized FPN1 in the PT. FPN1 was found to be located in association with the basolateral PT membrane and within the cytosolic compartment. FPN1 was not expressed on the apical brush-border membrane of PT cells. These data support a role for FPN1 in vectorial export of iron out of PT cells. Furthermore, under conditions of iron loading of cultured PT cells, FPN1 was trafficked to the plasma membrane suggesting a coordinated cellular response to export excess iron and limit cellular iron concentrations. © 2011 The Authors Journal of Cellular and Molecular Medicine © 2011 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd.
Original languageEnglish
Pages (from-to)209-219
Number of pages10
JournalJournal of cellular and molecular medicine
Volume15
Issue number2
DOIs
Publication statusPublished - Feb 2011

Keywords

  • Epithelial transport
  • Ferroportin 1
  • Iron homeostasis
  • Kidney
  • Proximal tubule

Fingerprint

Dive into the research topics of 'Ferroportin 1 is expressed basolaterally in rat kidney proximal tubule cells and iron excess increases its membrane trafficking'. Together they form a unique fingerprint.

Cite this