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Phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes

Phagocytes engulf unwanted particles into phagosomes that then fuse with lysosomes to degrade the enclosed particles. Ultimately, phagosomes must be recycled to help recover membrane resources that were consumed during phagocytosis and phagosome maturation, a process referred to as “phagosome resolu...

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Autores principales: Lancaster, Charlene E., Fountain, Aaron, Dayam, Roaya M., Somerville, Elliott, Sheth, Javal, Jacobelli, Vanessa, Somerville, Alex, Terebiznik, Mauricio R., Botelho, Roberto J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241537/
https://www.ncbi.nlm.nih.gov/pubmed/34180943
http://dx.doi.org/10.1083/jcb.202005072
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author Lancaster, Charlene E.
Fountain, Aaron
Dayam, Roaya M.
Somerville, Elliott
Sheth, Javal
Jacobelli, Vanessa
Somerville, Alex
Terebiznik, Mauricio R.
Botelho, Roberto J.
author_facet Lancaster, Charlene E.
Fountain, Aaron
Dayam, Roaya M.
Somerville, Elliott
Sheth, Javal
Jacobelli, Vanessa
Somerville, Alex
Terebiznik, Mauricio R.
Botelho, Roberto J.
author_sort Lancaster, Charlene E.
collection PubMed
description Phagocytes engulf unwanted particles into phagosomes that then fuse with lysosomes to degrade the enclosed particles. Ultimately, phagosomes must be recycled to help recover membrane resources that were consumed during phagocytosis and phagosome maturation, a process referred to as “phagosome resolution.” Little is known about phagosome resolution, which may proceed through exocytosis or membrane fission. Here, we show that bacteria-containing phagolysosomes in macrophages undergo fragmentation through vesicle budding, tubulation, and constriction. Phagosome fragmentation requires cargo degradation, the actin and microtubule cytoskeletons, and clathrin. We provide evidence that lysosome reformation occurs during phagosome resolution since the majority of phagosome-derived vesicles displayed lysosomal properties. Importantly, we show that clathrin-dependent phagosome resolution is important to maintain the degradative capacity of macrophages challenged with two waves of phagocytosis. Overall, our work suggests that phagosome resolution contributes to lysosome recovery and to maintaining the degradative power of macrophages to handle multiple waves of phagocytosis.
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spelling pubmed-82415372022-03-06 Phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes Lancaster, Charlene E. Fountain, Aaron Dayam, Roaya M. Somerville, Elliott Sheth, Javal Jacobelli, Vanessa Somerville, Alex Terebiznik, Mauricio R. Botelho, Roberto J. J Cell Biol Article Phagocytes engulf unwanted particles into phagosomes that then fuse with lysosomes to degrade the enclosed particles. Ultimately, phagosomes must be recycled to help recover membrane resources that were consumed during phagocytosis and phagosome maturation, a process referred to as “phagosome resolution.” Little is known about phagosome resolution, which may proceed through exocytosis or membrane fission. Here, we show that bacteria-containing phagolysosomes in macrophages undergo fragmentation through vesicle budding, tubulation, and constriction. Phagosome fragmentation requires cargo degradation, the actin and microtubule cytoskeletons, and clathrin. We provide evidence that lysosome reformation occurs during phagosome resolution since the majority of phagosome-derived vesicles displayed lysosomal properties. Importantly, we show that clathrin-dependent phagosome resolution is important to maintain the degradative capacity of macrophages challenged with two waves of phagocytosis. Overall, our work suggests that phagosome resolution contributes to lysosome recovery and to maintaining the degradative power of macrophages to handle multiple waves of phagocytosis. Rockefeller University Press 2021-06-28 /pmc/articles/PMC8241537/ /pubmed/34180943 http://dx.doi.org/10.1083/jcb.202005072 Text en © 2021 Lancaster et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Lancaster, Charlene E.
Fountain, Aaron
Dayam, Roaya M.
Somerville, Elliott
Sheth, Javal
Jacobelli, Vanessa
Somerville, Alex
Terebiznik, Mauricio R.
Botelho, Roberto J.
Phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes
title Phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes
title_full Phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes
title_fullStr Phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes
title_full_unstemmed Phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes
title_short Phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes
title_sort phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241537/
https://www.ncbi.nlm.nih.gov/pubmed/34180943
http://dx.doi.org/10.1083/jcb.202005072
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