Hartman Institute for Therapeutic Organ Regeneration

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

TitleThe fast-recycling receptor Megalin defines the apical recycling pathway of epithelial cells.
Publication TypeJournal Article
Year of Publication2016
AuthorsBay AEPerez, Schreiner R, Benedicto I, Marzolo MPaz, Banfelder J, Weinstein AM, Rodriguez-Boulan EJ
JournalNat Commun
Volume7
Pagination11550
Date Published2016 May 16
ISSN2041-1723
KeywordsAnimals, Cell Polarity, Dogs, Endocytosis, Endosomes, Epithelial Cells, Kinetics, Low Density Lipoprotein Receptor-Related Protein-2, Madin Darby Canine Kidney Cells, Microtubules, Models, Biological, Proteolysis, rab GTP-Binding Proteins
Abstract

<p>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.</p>

DOI10.1038/ncomms11550
Alternate JournalNat Commun
PubMed ID27180806
PubMed Central IDPMC4873671
Grant ListK01 DK102836 / DK / NIDDK NIH HHS / United States
R01 DK029857 / DK / NIDDK NIH HHS / United States
R01 EY008538 / EY / NEI NIH HHS / United States
R01 GM034107 / GM / NIGMS NIH HHS / United States

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Hartman Institute for Therapeutic Organ Regeneration
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