<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>104(47)</volume><submitter>Rogers LD</submitter><pubmed_abstract>Macrophages use phagocytosis to control the spread of pathogens in the body, to clear apoptotic cells, and to aid in tissue remodeling. The phagosomal membrane is traditionally thought to originate from the plasmalemma and then go through a series of maturation steps involving sequential fusion with endosomal compartments, leading to the formation of a phagolysosome. A recent model suggests that the endoplasmic reticulum (ER) is involved in the maturation as well. Here we use stable isotope labeling and multiple quantitative proteomic approaches to follow the dynamic composition of the maturing phagosome in RAW 264.7 macrophage cells to a greater depth and higher temporal resolution than was previously possible. Analysis of the results suggests that the traditional model of a linear sequen</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>18520-5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2141809</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The dynamic phagosomal proteome and the contribution of the endoplasmic reticulum.</pubmed_title><pmcid>PMC2141809</pmcid><pubmed_authors>Rogers LD</pubmed_authors><pubmed_authors>Foster LJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>The dynamic phagosomal proteome and the contribution of the endoplasmic reticulum.</name><description>Macrophages use phagocytosis to control the spread of pathogens in the body, to clear apoptotic cells, and to aid in tissue remodeling. The phagosomal membrane is traditionally thought to originate from the plasmalemma and then go through a series of maturation steps involving sequential fusion with endosomal compartments, leading to the formation of a phagolysosome. A recent model suggests that the endoplasmic reticulum (ER) is involved in the maturation as well. Here we use stable isotope labeling and multiple quantitative proteomic approaches to follow the dynamic composition of the maturing phagosome in RAW 264.7 macrophage cells to a greater depth and higher temporal resolution than was previously possible. Analysis of the results suggests that the traditional model of a linear sequen</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Nov</publication><modification>2026-04-29T19:50:49.307Z</modification><creation>2019-03-27T02:22:09Z</creation></dates><accession>S-EPMC2141809</accession><cross_references><pubmed>18006660</pubmed><doi>10.1073/pnas.0705801104</doi></cross_references></HashMap>