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Transferrin receptor 1 is a cellular receptor for human heme-albumin
Iron is essential for living cells. Uptake of iron-loaded transferrin by the transferrin receptor 1 (CD71, TFR) is a major but not sufficient mechanism and an alternative iron-loaded ligand for CD71 has been assumed. Here, we demonstrate that CD71 utilizes heme-albumin as cargo to transport iron int...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591885/ https://www.ncbi.nlm.nih.gov/pubmed/33110194 http://dx.doi.org/10.1038/s42003-020-01294-5 |
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author | Jennifer, Brell Berg, Verena Modak, Madhura Puck, Alexander Seyerl-Jiresch, Maria Künig, Sarojinidevi Zlabinger, Gerhard J. Steinberger, Peter Chou, Janet Geha, Raif S. Öhler, Leopold Yachie, Akihiro Choe, Hyeryun Kraller, Markus Stockinger, Hannes Stöckl, Johannes |
author_facet | Jennifer, Brell Berg, Verena Modak, Madhura Puck, Alexander Seyerl-Jiresch, Maria Künig, Sarojinidevi Zlabinger, Gerhard J. Steinberger, Peter Chou, Janet Geha, Raif S. Öhler, Leopold Yachie, Akihiro Choe, Hyeryun Kraller, Markus Stockinger, Hannes Stöckl, Johannes |
author_sort | Jennifer, Brell |
collection | PubMed |
description | Iron is essential for living cells. Uptake of iron-loaded transferrin by the transferrin receptor 1 (CD71, TFR) is a major but not sufficient mechanism and an alternative iron-loaded ligand for CD71 has been assumed. Here, we demonstrate that CD71 utilizes heme-albumin as cargo to transport iron into human cells. Binding and endocytosis of heme-albumin via CD71 was sufficient to promote proliferation of various cell types in the absence of transferrin. Growth and differentiation of cells induced by heme-albumin was dependent on heme-oxygenase 1 (HO-1) function and was accompanied with an increase of the intracellular labile iron pool (LIP). Import of heme-albumin via CD71 was further found to contribute to the efficacy of albumin-based drugs such as the chemotherapeutic Abraxane. Thus, heme-albumin/CD71 interaction is a novel route to transport nutrients or drugs into cells and adds to the emerging function of CD71 as a scavenger receptor. |
format | Online Article Text |
id | pubmed-7591885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75918852020-10-29 Transferrin receptor 1 is a cellular receptor for human heme-albumin Jennifer, Brell Berg, Verena Modak, Madhura Puck, Alexander Seyerl-Jiresch, Maria Künig, Sarojinidevi Zlabinger, Gerhard J. Steinberger, Peter Chou, Janet Geha, Raif S. Öhler, Leopold Yachie, Akihiro Choe, Hyeryun Kraller, Markus Stockinger, Hannes Stöckl, Johannes Commun Biol Article Iron is essential for living cells. Uptake of iron-loaded transferrin by the transferrin receptor 1 (CD71, TFR) is a major but not sufficient mechanism and an alternative iron-loaded ligand for CD71 has been assumed. Here, we demonstrate that CD71 utilizes heme-albumin as cargo to transport iron into human cells. Binding and endocytosis of heme-albumin via CD71 was sufficient to promote proliferation of various cell types in the absence of transferrin. Growth and differentiation of cells induced by heme-albumin was dependent on heme-oxygenase 1 (HO-1) function and was accompanied with an increase of the intracellular labile iron pool (LIP). Import of heme-albumin via CD71 was further found to contribute to the efficacy of albumin-based drugs such as the chemotherapeutic Abraxane. Thus, heme-albumin/CD71 interaction is a novel route to transport nutrients or drugs into cells and adds to the emerging function of CD71 as a scavenger receptor. Nature Publishing Group UK 2020-10-27 /pmc/articles/PMC7591885/ /pubmed/33110194 http://dx.doi.org/10.1038/s42003-020-01294-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jennifer, Brell Berg, Verena Modak, Madhura Puck, Alexander Seyerl-Jiresch, Maria Künig, Sarojinidevi Zlabinger, Gerhard J. Steinberger, Peter Chou, Janet Geha, Raif S. Öhler, Leopold Yachie, Akihiro Choe, Hyeryun Kraller, Markus Stockinger, Hannes Stöckl, Johannes Transferrin receptor 1 is a cellular receptor for human heme-albumin |
title | Transferrin receptor 1 is a cellular receptor for human heme-albumin |
title_full | Transferrin receptor 1 is a cellular receptor for human heme-albumin |
title_fullStr | Transferrin receptor 1 is a cellular receptor for human heme-albumin |
title_full_unstemmed | Transferrin receptor 1 is a cellular receptor for human heme-albumin |
title_short | Transferrin receptor 1 is a cellular receptor for human heme-albumin |
title_sort | transferrin receptor 1 is a cellular receptor for human heme-albumin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591885/ https://www.ncbi.nlm.nih.gov/pubmed/33110194 http://dx.doi.org/10.1038/s42003-020-01294-5 |
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