Cited by 47Iron Metabolism and DisordersFerroptosis and cancer prognosisTrace Elements in Health

Apical location of ferroportin 1 in airway epithelia and its role in iron detoxification in the lung

Yang, Funmei, Haile, David J., Wang, Xinchao, Dailey, Lisa A., Stonehuerner, Jacqueline G., Ghio, Andrew J.·2005·American Journal of Physiology-Lung Cellular and Molecular Physiology

Abstract

Ferroportin 1 (FPN1; aka MTP1, IREG1, and SLC40A1), which was originally identified as a basolateral iron transporter crucial for nutritional iron absorption in the intestine, is expressed in airway epithelia and upregulated when these cells are exposed to iron. Using immunofluorescence labeling and confocal microscopic imaging techniques, we demonstrate that in human and rodent lungs, FPN1 localizes subcellularly to the apical but not basolateral membrane of the airway epithelial cells. The role of airway epithelial cells in iron mobilization in the lung was studied in an in vitro model of the polarized airway epithelium. Normal human bronchial epithelial cells, grown on membrane supports until differentiated, were exposed to iron, and the efficiency and direction of iron transportation were studied. We found that these cells can efficiently take up iron across the apical but not basolateral surface in a concentration-dependent manner. Most of the iron taken up by the cells is then released into the medium within 8 h in the form of less reactive protein-bound complexes including ferritin and transferrin. Interestingly, iron release also occurred across the apical but not basolateral membrane. Our findings indicate that FPN1, depending on its subcellular location, could have distinct functions in iron homeostasis in different cells and tissues. Although it is responsible for exporting nutrient iron from enterocytes to the circulation in the intestine, it could play a role in iron detoxification in airway epithelial cells in the lung.

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Crossref · 10.1152/ajplung.00456.2004

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  • Airway epithelial cells may be efficient in reducing non-transferrin-bound iron, converting it to less toxic protein-bound iron.

    “The airway epithelial cells, acting as the first line defence against environmental insults, including asbestos, may be efficient in reducing non-transferrin-bound iron, converting it to less toxic protein-bound iron2122.”

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Authors
Yang, F., Haile, D. J., Wang, X., Dailey, L. A., Stonehuerner, J. G., & Ghio, A. J.
Affiliations
  • The University of Texas at San Antonio Health Science Center (US)
  • Environmental Protection Agency (US)
Venue
American Journal of Physiology-Lung Cellular and Molecular Physiology
Published
2005-07
Volume
289
Issue
1
Pages
L14-L23
ISSN
  • 1040-0605 (ISSN-L)
  • 1522-1504
OpenAlex
W2168157030
Cited by
47
References
39
Citations by year
2026: 3 · 2025: 1 · 2024: 1 · 2022: 2 · 2021: 3 · 2020: 2 · 2019: 2 · 2018: 2 · 2017: 3 · 2015: 2 · 2014: 2 · 2013: 3 · 2012: 4
FWCI
2.34
Type
journal article
Language
en
Open access
closed
Locations
  • American Journal of Physiology-Lung Cellular and Molecular Physiology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01dk053079-02, 5r01hl068842-04)
  • University of Texas Health Science Center at San Antonio
  • National Heart, Lung, and Blood Institute (R01HL-68842)
  • National Institute of Diabetes and Digestive and Kidney Diseases (R01DK-53079)
Topics
  • Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Ferroptosis and cancer prognosis
  • Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
Keywords
ferroportin 1, apical membrane localization, airway epithelium, iron homeostasis, iron detoxification, iron transport, iron export, bronchial epithelial cells, ferritin, transferrin, intracellular trafficking
MeSH terms
Ferroportin, Animals, Biological Transport, Active, Cell Line, Cell Membrane, Dose-Response Relationship, Drug, Epithelial Cells, Epithelium, Ferritins, Humans, Intestinal Mucosa, Iron, Lung, Inactivation, Metabolic, Transferrin, Gene Expression, Cation Transport Proteins, Mice

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