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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2016
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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. |
format | Online Article Text |
id | pubmed-4694750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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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