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Macropinocytosis is responsible for the uptake of pathogenic and non-pathogenic mycobacteria by B lymphocytes (Raji cells)
BACKGROUND: The classical roles of B cells include the production of antibodies and cytokines and the generation of immunological memory, these being key factors in the adaptive immune response. However, their role in innate immunity is currently being recognised. Traditionally, B cells have been co...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559283/ https://www.ncbi.nlm.nih.gov/pubmed/23113903 http://dx.doi.org/10.1186/1471-2180-12-246 |
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author | García-Pérez, Blanca Estela De la Cruz-López, Juan José Castañeda-Sánchez, Jorge Ismael Muñóz-Duarte, Ana Rosa Hernández-Pérez, Alma Delia Villegas-Castrejón, Hilda García-Latorre, Ethel Caamal-Ley, Angel Luna-Herrera, Julieta |
author_facet | García-Pérez, Blanca Estela De la Cruz-López, Juan José Castañeda-Sánchez, Jorge Ismael Muñóz-Duarte, Ana Rosa Hernández-Pérez, Alma Delia Villegas-Castrejón, Hilda García-Latorre, Ethel Caamal-Ley, Angel Luna-Herrera, Julieta |
author_sort | García-Pérez, Blanca Estela |
collection | PubMed |
description | BACKGROUND: The classical roles of B cells include the production of antibodies and cytokines and the generation of immunological memory, these being key factors in the adaptive immune response. However, their role in innate immunity is currently being recognised. Traditionally, B cells have been considered non-phagocytic cells; therefore, the uptake of bacteria by B cells is not extensively documented. In this study, we analysed some of the features of non-specific bacterial uptake by B lymphocytes from the Raji cell line. In our model, B cells were infected with Mycobacterium tuberculosis (MTB), Mycobacterium smegmatis (MSM), and Salmonella typhimurium (ST). RESULTS: Our observations revealed that the Raji B cells were readily infected by the three bacteria that were studied. All of the infections induced changes in the cellular membrane during bacterial internalisation. M. smegmatis and S. typhimurium were able to induce important membrane changes that were characterised by abundant filopodia and lamellipodia formation. These membrane changes were driven by actin cytoskeletal rearrangements. The intracellular growth of these bacteria was also controlled by B cells. M. tuberculosis infection also induced actin rearrangement-driven membrane changes; however, the B cells were not able to control this infection. The phorbol 12-myristate 13-acetate (PMA) treatment of B cells induced filopodia and lamellipodia formation, the production of spacious vacuoles (macropinosomes), and the fluid-phase uptake that is characteristic of macropinocytosis. S. typhimurium infection induced the highest fluid-phase uptake, although both mycobacteria also induced fluid uptake. A macropinocytosis inhibitor such as amiloride was used and abolished the bacterial uptake and the fluid-phase uptake that is triggered during the bacterial infection. CONCLUSIONS: Raji B cells can internalise S. typhimurium and mycobacteria through an active process, such as macropinocytosis, although the resolution of the infection depends on factors that are inherent in the virulence of each pathogen. |
format | Online Article Text |
id | pubmed-3559283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35592832013-02-01 Macropinocytosis is responsible for the uptake of pathogenic and non-pathogenic mycobacteria by B lymphocytes (Raji cells) García-Pérez, Blanca Estela De la Cruz-López, Juan José Castañeda-Sánchez, Jorge Ismael Muñóz-Duarte, Ana Rosa Hernández-Pérez, Alma Delia Villegas-Castrejón, Hilda García-Latorre, Ethel Caamal-Ley, Angel Luna-Herrera, Julieta BMC Microbiol Research Article BACKGROUND: The classical roles of B cells include the production of antibodies and cytokines and the generation of immunological memory, these being key factors in the adaptive immune response. However, their role in innate immunity is currently being recognised. Traditionally, B cells have been considered non-phagocytic cells; therefore, the uptake of bacteria by B cells is not extensively documented. In this study, we analysed some of the features of non-specific bacterial uptake by B lymphocytes from the Raji cell line. In our model, B cells were infected with Mycobacterium tuberculosis (MTB), Mycobacterium smegmatis (MSM), and Salmonella typhimurium (ST). RESULTS: Our observations revealed that the Raji B cells were readily infected by the three bacteria that were studied. All of the infections induced changes in the cellular membrane during bacterial internalisation. M. smegmatis and S. typhimurium were able to induce important membrane changes that were characterised by abundant filopodia and lamellipodia formation. These membrane changes were driven by actin cytoskeletal rearrangements. The intracellular growth of these bacteria was also controlled by B cells. M. tuberculosis infection also induced actin rearrangement-driven membrane changes; however, the B cells were not able to control this infection. The phorbol 12-myristate 13-acetate (PMA) treatment of B cells induced filopodia and lamellipodia formation, the production of spacious vacuoles (macropinosomes), and the fluid-phase uptake that is characteristic of macropinocytosis. S. typhimurium infection induced the highest fluid-phase uptake, although both mycobacteria also induced fluid uptake. A macropinocytosis inhibitor such as amiloride was used and abolished the bacterial uptake and the fluid-phase uptake that is triggered during the bacterial infection. CONCLUSIONS: Raji B cells can internalise S. typhimurium and mycobacteria through an active process, such as macropinocytosis, although the resolution of the infection depends on factors that are inherent in the virulence of each pathogen. BioMed Central 2012-10-31 /pmc/articles/PMC3559283/ /pubmed/23113903 http://dx.doi.org/10.1186/1471-2180-12-246 Text en Copyright ©2012 García-Pérez et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article García-Pérez, Blanca Estela De la Cruz-López, Juan José Castañeda-Sánchez, Jorge Ismael Muñóz-Duarte, Ana Rosa Hernández-Pérez, Alma Delia Villegas-Castrejón, Hilda García-Latorre, Ethel Caamal-Ley, Angel Luna-Herrera, Julieta Macropinocytosis is responsible for the uptake of pathogenic and non-pathogenic mycobacteria by B lymphocytes (Raji cells) |
title | Macropinocytosis is responsible for the uptake of pathogenic and non-pathogenic mycobacteria by B lymphocytes (Raji cells) |
title_full | Macropinocytosis is responsible for the uptake of pathogenic and non-pathogenic mycobacteria by B lymphocytes (Raji cells) |
title_fullStr | Macropinocytosis is responsible for the uptake of pathogenic and non-pathogenic mycobacteria by B lymphocytes (Raji cells) |
title_full_unstemmed | Macropinocytosis is responsible for the uptake of pathogenic and non-pathogenic mycobacteria by B lymphocytes (Raji cells) |
title_short | Macropinocytosis is responsible for the uptake of pathogenic and non-pathogenic mycobacteria by B lymphocytes (Raji cells) |
title_sort | macropinocytosis is responsible for the uptake of pathogenic and non-pathogenic mycobacteria by b lymphocytes (raji cells) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559283/ https://www.ncbi.nlm.nih.gov/pubmed/23113903 http://dx.doi.org/10.1186/1471-2180-12-246 |
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