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The fast-recycling receptor Megalin defines the apical recycling pathway of epithelial cells

The basolateral recycling and transcytotic pathways of epithelial cells were previously defined using markers such as transferrin (TfR) and polymeric IgA (pIgR) receptors. In contrast, our knowledge of the apical recycling pathway remains fragmentary. Here we utilize quantitative live-imaging and ma...

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Autores principales: Perez Bay, Andres E., Schreiner, Ryan, Benedicto, Ignacio, Paz Marzolo, Maria, Banfelder, Jason, Weinstein, Alan M., Rodriguez-Boulan, Enrique J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873671/
https://www.ncbi.nlm.nih.gov/pubmed/27180806
http://dx.doi.org/10.1038/ncomms11550
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author Perez Bay, Andres E.
Schreiner, Ryan
Benedicto, Ignacio
Paz Marzolo, Maria
Banfelder, Jason
Weinstein, Alan M.
Rodriguez-Boulan, Enrique J.
author_facet Perez Bay, Andres E.
Schreiner, Ryan
Benedicto, Ignacio
Paz Marzolo, Maria
Banfelder, Jason
Weinstein, Alan M.
Rodriguez-Boulan, Enrique J.
author_sort Perez Bay, Andres E.
collection PubMed
description The basolateral recycling and transcytotic pathways of epithelial cells were previously defined using markers such as transferrin (TfR) and polymeric IgA (pIgR) receptors. In contrast, our knowledge of the apical recycling pathway remains fragmentary. Here we utilize quantitative live-imaging and mathematical modelling to outline the recycling pathway of Megalin (LRP-2), an apical receptor with key developmental and renal functions, in MDCK cells. We show that, like TfR, Megalin is a long-lived and fast-recycling receptor. Megalin enters polarized MDCK cells through segregated apical sorting endosomes and subsequently intersects the TfR and pIgR pathways at a perinuclear Rab11-negative compartment termed common recycling endosomes (CRE). Whereas TfR recycles to the basolateral membrane from CRE, Megalin, like pIgR, traffics to subapical Rab11-positive apical recycling endosomes (ARE) and reaches the apical membrane in a microtubule- and Rab11-dependent manner. Hence, Megalin defines the apical recycling pathway of epithelia, with CRE as its apical sorting station.
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spelling pubmed-48736712016-06-02 The fast-recycling receptor Megalin defines the apical recycling pathway of epithelial cells Perez Bay, Andres E. Schreiner, Ryan Benedicto, Ignacio Paz Marzolo, Maria Banfelder, Jason Weinstein, Alan M. Rodriguez-Boulan, Enrique J. Nat Commun Article The basolateral recycling and transcytotic pathways of epithelial cells were previously defined using markers such as transferrin (TfR) and polymeric IgA (pIgR) receptors. In contrast, our knowledge of the apical recycling pathway remains fragmentary. Here we utilize quantitative live-imaging and mathematical modelling to outline the recycling pathway of Megalin (LRP-2), an apical receptor with key developmental and renal functions, in MDCK cells. We show that, like TfR, Megalin is a long-lived and fast-recycling receptor. Megalin enters polarized MDCK cells through segregated apical sorting endosomes and subsequently intersects the TfR and pIgR pathways at a perinuclear Rab11-negative compartment termed common recycling endosomes (CRE). Whereas TfR recycles to the basolateral membrane from CRE, Megalin, like pIgR, traffics to subapical Rab11-positive apical recycling endosomes (ARE) and reaches the apical membrane in a microtubule- and Rab11-dependent manner. Hence, Megalin defines the apical recycling pathway of epithelia, with CRE as its apical sorting station. Nature Publishing Group 2016-05-16 /pmc/articles/PMC4873671/ /pubmed/27180806 http://dx.doi.org/10.1038/ncomms11550 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Perez Bay, Andres E.
Schreiner, Ryan
Benedicto, Ignacio
Paz Marzolo, Maria
Banfelder, Jason
Weinstein, Alan M.
Rodriguez-Boulan, Enrique J.
The fast-recycling receptor Megalin defines the apical recycling pathway of epithelial cells
title The fast-recycling receptor Megalin defines the apical recycling pathway of epithelial cells
title_full The fast-recycling receptor Megalin defines the apical recycling pathway of epithelial cells
title_fullStr The fast-recycling receptor Megalin defines the apical recycling pathway of epithelial cells
title_full_unstemmed The fast-recycling receptor Megalin defines the apical recycling pathway of epithelial cells
title_short The fast-recycling receptor Megalin defines the apical recycling pathway of epithelial cells
title_sort fast-recycling receptor megalin defines the apical recycling pathway of epithelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873671/
https://www.ncbi.nlm.nih.gov/pubmed/27180806
http://dx.doi.org/10.1038/ncomms11550
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