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High‐resolution quantitative proteome analysis reveals substantial differences between phagosomes of RAW 264.7 and bone marrow derived macrophages

Macrophages are important immune cells operating at the forefront of innate immunity by taking up foreign particles and microbes through phagocytosis. The RAW 264.7 cell line is commonly used for experiments in the macrophage and phagocytosis field. However, little is known how its functions compare...

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Autores principales: Guo, Manman, Härtlova, Anetta, Dill, Brian D., Prescott, Alan R., Gierliński, Marek, Trost, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833182/
https://www.ncbi.nlm.nih.gov/pubmed/25504905
http://dx.doi.org/10.1002/pmic.201400431
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author Guo, Manman
Härtlova, Anetta
Dill, Brian D.
Prescott, Alan R.
Gierliński, Marek
Trost, Matthias
author_facet Guo, Manman
Härtlova, Anetta
Dill, Brian D.
Prescott, Alan R.
Gierliński, Marek
Trost, Matthias
author_sort Guo, Manman
collection PubMed
description Macrophages are important immune cells operating at the forefront of innate immunity by taking up foreign particles and microbes through phagocytosis. The RAW 264.7 cell line is commonly used for experiments in the macrophage and phagocytosis field. However, little is known how its functions compare to primary macrophages. Here, we have performed an in‐depth proteomics characterization of phagosomes from RAW 264.7 and bone marrow derived macrophages by quantifying more than 2500 phagosomal proteins. Our data indicate that there are significant differences for a large number of proteins including important receptors such as mannose receptor 1 and Siglec‐1. Moreover, bone marrow derived macrophages phagosomes mature considerably faster by fusion with endosomes and the lysosome which we validated using fluorogenic phagocytic assays. We provide a valuable resource for researcher in the field and recommend careful use of the RAW 264.7 cell line when studying phagosome functions. All MS data have been deposited in the ProteomeXchange with identifier PXD001293 (http://proteomecentral.proteomexchange.org/dataset/PXD001293).
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spelling pubmed-48331822016-06-24 High‐resolution quantitative proteome analysis reveals substantial differences between phagosomes of RAW 264.7 and bone marrow derived macrophages Guo, Manman Härtlova, Anetta Dill, Brian D. Prescott, Alan R. Gierliński, Marek Trost, Matthias Proteomics Dataset Brief Macrophages are important immune cells operating at the forefront of innate immunity by taking up foreign particles and microbes through phagocytosis. The RAW 264.7 cell line is commonly used for experiments in the macrophage and phagocytosis field. However, little is known how its functions compare to primary macrophages. Here, we have performed an in‐depth proteomics characterization of phagosomes from RAW 264.7 and bone marrow derived macrophages by quantifying more than 2500 phagosomal proteins. Our data indicate that there are significant differences for a large number of proteins including important receptors such as mannose receptor 1 and Siglec‐1. Moreover, bone marrow derived macrophages phagosomes mature considerably faster by fusion with endosomes and the lysosome which we validated using fluorogenic phagocytic assays. We provide a valuable resource for researcher in the field and recommend careful use of the RAW 264.7 cell line when studying phagosome functions. All MS data have been deposited in the ProteomeXchange with identifier PXD001293 (http://proteomecentral.proteomexchange.org/dataset/PXD001293). John Wiley and Sons Inc. 2015-02-05 2015-09 /pmc/articles/PMC4833182/ /pubmed/25504905 http://dx.doi.org/10.1002/pmic.201400431 Text en © 2014 The Authors. PROTEOMICS published by Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Dataset Brief
Guo, Manman
Härtlova, Anetta
Dill, Brian D.
Prescott, Alan R.
Gierliński, Marek
Trost, Matthias
High‐resolution quantitative proteome analysis reveals substantial differences between phagosomes of RAW 264.7 and bone marrow derived macrophages
title High‐resolution quantitative proteome analysis reveals substantial differences between phagosomes of RAW 264.7 and bone marrow derived macrophages
title_full High‐resolution quantitative proteome analysis reveals substantial differences between phagosomes of RAW 264.7 and bone marrow derived macrophages
title_fullStr High‐resolution quantitative proteome analysis reveals substantial differences between phagosomes of RAW 264.7 and bone marrow derived macrophages
title_full_unstemmed High‐resolution quantitative proteome analysis reveals substantial differences between phagosomes of RAW 264.7 and bone marrow derived macrophages
title_short High‐resolution quantitative proteome analysis reveals substantial differences between phagosomes of RAW 264.7 and bone marrow derived macrophages
title_sort high‐resolution quantitative proteome analysis reveals substantial differences between phagosomes of raw 264.7 and bone marrow derived macrophages
topic Dataset Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833182/
https://www.ncbi.nlm.nih.gov/pubmed/25504905
http://dx.doi.org/10.1002/pmic.201400431
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