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The endocytic recycling compartment maintains cargo segregation acquired upon exit from the sorting endosome

The endocytic recycling compartment (ERC) is a series of perinuclear tubular and vesicular membranes that regulates recycling to the plasma membrane. Despite evidence that cargo is sorted at the early/sorting endosome (SE), whether cargo mixes downstream at the ERC or remains segregated is an unansw...

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Autores principales: Xie, Shuwei, Bahl, Kriti, Reinecke, James B., Hammond, Gerald R. V., Naslavsky, Naava, Caplan, Steve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694750/
https://www.ncbi.nlm.nih.gov/pubmed/26510502
http://dx.doi.org/10.1091/mbc.E15-07-0514
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author Xie, Shuwei
Bahl, Kriti
Reinecke, James B.
Hammond, Gerald R. V.
Naslavsky, Naava
Caplan, Steve
author_facet Xie, Shuwei
Bahl, Kriti
Reinecke, James B.
Hammond, Gerald R. V.
Naslavsky, Naava
Caplan, Steve
author_sort Xie, Shuwei
collection PubMed
description The endocytic recycling compartment (ERC) is a series of perinuclear tubular and vesicular membranes that regulates recycling to the plasma membrane. Despite evidence that cargo is sorted at the early/sorting endosome (SE), whether cargo mixes downstream at the ERC or remains segregated is an unanswered question. Here we use three-dimensional (3D) structured illumination microscopy and dual-channel and 3D direct stochastic optical reconstruction microscopy (dSTORM) to obtain new information about ERC morphology and cargo segregation. We show that cargo internalized either via clathrin-mediated endocytosis (CME) or independently of clathrin (CIE) remains segregated in the ERC, likely on distinct carriers. This suggests that no further sorting occurs upon cargo exit from SE. Moreover, 3D dSTORM data support a model in which some but not all ERC vesicles are tethered by contiguous “membrane bridges.” Furthermore, tubular recycling endosomes preferentially traffic CIE cargo and may originate from SE membranes. These findings support a significantly altered model for endocytic recycling in mammalian cells in which sorting occurs in peripheral endosomes and segregation is maintained at the ERC.
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spelling pubmed-46947502016-03-16 The endocytic recycling compartment maintains cargo segregation acquired upon exit from the sorting endosome Xie, Shuwei Bahl, Kriti Reinecke, James B. Hammond, Gerald R. V. Naslavsky, Naava Caplan, Steve Mol Biol Cell Articles The endocytic recycling compartment (ERC) is a series of perinuclear tubular and vesicular membranes that regulates recycling to the plasma membrane. Despite evidence that cargo is sorted at the early/sorting endosome (SE), whether cargo mixes downstream at the ERC or remains segregated is an unanswered question. Here we use three-dimensional (3D) structured illumination microscopy and dual-channel and 3D direct stochastic optical reconstruction microscopy (dSTORM) to obtain new information about ERC morphology and cargo segregation. We show that cargo internalized either via clathrin-mediated endocytosis (CME) or independently of clathrin (CIE) remains segregated in the ERC, likely on distinct carriers. This suggests that no further sorting occurs upon cargo exit from SE. Moreover, 3D dSTORM data support a model in which some but not all ERC vesicles are tethered by contiguous “membrane bridges.” Furthermore, tubular recycling endosomes preferentially traffic CIE cargo and may originate from SE membranes. These findings support a significantly altered model for endocytic recycling in mammalian cells in which sorting occurs in peripheral endosomes and segregation is maintained at the ERC. The American Society for Cell Biology 2016-01-01 /pmc/articles/PMC4694750/ /pubmed/26510502 http://dx.doi.org/10.1091/mbc.E15-07-0514 Text en © 2016 Xie et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Xie, Shuwei
Bahl, Kriti
Reinecke, James B.
Hammond, Gerald R. V.
Naslavsky, Naava
Caplan, Steve
The endocytic recycling compartment maintains cargo segregation acquired upon exit from the sorting endosome
title The endocytic recycling compartment maintains cargo segregation acquired upon exit from the sorting endosome
title_full The endocytic recycling compartment maintains cargo segregation acquired upon exit from the sorting endosome
title_fullStr The endocytic recycling compartment maintains cargo segregation acquired upon exit from the sorting endosome
title_full_unstemmed The endocytic recycling compartment maintains cargo segregation acquired upon exit from the sorting endosome
title_short The endocytic recycling compartment maintains cargo segregation acquired upon exit from the sorting endosome
title_sort endocytic recycling compartment maintains cargo segregation acquired upon exit from the sorting endosome
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694750/
https://www.ncbi.nlm.nih.gov/pubmed/26510502
http://dx.doi.org/10.1091/mbc.E15-07-0514
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