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Proteomic Analysis of Lipid Rafts from RBL-2H3 Mast Cells
Lipid rafts are highly ordered membrane microdomains enriched in cholesterol, glycosphingolipids, and certain proteins. They are involved in the regulation of cellular processes in diverse cell types, including mast cells (MCs). The MC lipid raft protein composition was assessed using qualitative ma...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720779/ https://www.ncbi.nlm.nih.gov/pubmed/31405203 http://dx.doi.org/10.3390/ijms20163904 |
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author | Freitas Filho, Edismauro Garcia Jaca, Luiz Augusto Marin Baeza, Lilian Cristiane Soares, Célia Maria de Almeida Borges, Clayton Luiz Oliver, Constance Jamur, Maria Célia |
author_facet | Freitas Filho, Edismauro Garcia Jaca, Luiz Augusto Marin Baeza, Lilian Cristiane Soares, Célia Maria de Almeida Borges, Clayton Luiz Oliver, Constance Jamur, Maria Célia |
author_sort | Freitas Filho, Edismauro Garcia |
collection | PubMed |
description | Lipid rafts are highly ordered membrane microdomains enriched in cholesterol, glycosphingolipids, and certain proteins. They are involved in the regulation of cellular processes in diverse cell types, including mast cells (MCs). The MC lipid raft protein composition was assessed using qualitative mass spectrometric characterization of the proteome from detergent-resistant membrane fractions from RBL-2H3 MCs. Using two different post-isolation treatment methods, a total of 949 lipid raft associated proteins were identified. The majority of these MC lipid raft proteins had already been described in the RaftProtV2 database and are among highest cited/experimentally validated lipid raft proteins. Additionally, more than half of the identified proteins had lipid modifications and/or transmembrane domains. Classification of identified proteins into functional categories showed that the proteins were associated with cellular membrane compartments, and with some biological and molecular functions, such as regulation, localization, binding, catalytic activity, and response to stimulus. Furthermore, functional enrichment analysis demonstrated an intimate involvement of identified proteins with various aspects of MC biological processes, especially those related to regulated secretion, organization/stabilization of macromolecules complexes, and signal transduction. This study represents the first comprehensive proteomic profile of MC lipid rafts and provides additional information to elucidate immunoregulatory functions coordinated by raft proteins in MCs. |
format | Online Article Text |
id | pubmed-6720779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67207792019-09-10 Proteomic Analysis of Lipid Rafts from RBL-2H3 Mast Cells Freitas Filho, Edismauro Garcia Jaca, Luiz Augusto Marin Baeza, Lilian Cristiane Soares, Célia Maria de Almeida Borges, Clayton Luiz Oliver, Constance Jamur, Maria Célia Int J Mol Sci Article Lipid rafts are highly ordered membrane microdomains enriched in cholesterol, glycosphingolipids, and certain proteins. They are involved in the regulation of cellular processes in diverse cell types, including mast cells (MCs). The MC lipid raft protein composition was assessed using qualitative mass spectrometric characterization of the proteome from detergent-resistant membrane fractions from RBL-2H3 MCs. Using two different post-isolation treatment methods, a total of 949 lipid raft associated proteins were identified. The majority of these MC lipid raft proteins had already been described in the RaftProtV2 database and are among highest cited/experimentally validated lipid raft proteins. Additionally, more than half of the identified proteins had lipid modifications and/or transmembrane domains. Classification of identified proteins into functional categories showed that the proteins were associated with cellular membrane compartments, and with some biological and molecular functions, such as regulation, localization, binding, catalytic activity, and response to stimulus. Furthermore, functional enrichment analysis demonstrated an intimate involvement of identified proteins with various aspects of MC biological processes, especially those related to regulated secretion, organization/stabilization of macromolecules complexes, and signal transduction. This study represents the first comprehensive proteomic profile of MC lipid rafts and provides additional information to elucidate immunoregulatory functions coordinated by raft proteins in MCs. MDPI 2019-08-11 /pmc/articles/PMC6720779/ /pubmed/31405203 http://dx.doi.org/10.3390/ijms20163904 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Freitas Filho, Edismauro Garcia Jaca, Luiz Augusto Marin Baeza, Lilian Cristiane Soares, Célia Maria de Almeida Borges, Clayton Luiz Oliver, Constance Jamur, Maria Célia Proteomic Analysis of Lipid Rafts from RBL-2H3 Mast Cells |
title | Proteomic Analysis of Lipid Rafts from RBL-2H3 Mast Cells |
title_full | Proteomic Analysis of Lipid Rafts from RBL-2H3 Mast Cells |
title_fullStr | Proteomic Analysis of Lipid Rafts from RBL-2H3 Mast Cells |
title_full_unstemmed | Proteomic Analysis of Lipid Rafts from RBL-2H3 Mast Cells |
title_short | Proteomic Analysis of Lipid Rafts from RBL-2H3 Mast Cells |
title_sort | proteomic analysis of lipid rafts from rbl-2h3 mast cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720779/ https://www.ncbi.nlm.nih.gov/pubmed/31405203 http://dx.doi.org/10.3390/ijms20163904 |
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