Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation?
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1371/journal.pone.0034570 http://repositorio.unifesp.br/handle/11600/34721 |
Resumo: | The inflammatory response is driven by signals that recruit and elicit immune cells to areas of tissue damage or infection. the concept of a mononuclear phagocyte system postulates that monocytes circulating in the bloodstream are recruited to inflamed tissues where they give rise to macrophages. A recent publication demonstrated that the large increase in the macrophages observed during infection was the result of the multiplication of these cells rather than the recruitment of blood monocytes. We demonstrated previously that B-1 cells undergo differentiation to acquire a mononuclear phagocyte phenotype in vitro (B-1CDP), and we propose that B-1 cells could be an alternative origin for peritoneal macrophages. A number of recent studies that describe the phagocytic and microbicidal activity of B-1 cells in vitro and in vivo support this hypothesis. Based on these findings, we further investigated the differentiation of B-1 cells into phagocytes in vivo in response to LPS-induced inflammation. Therefore, we investigated the role of B-1 cells in the composition of the peritoneal macrophage population after LPS stimulation using osteopetrotic mice, BALB/Xid mice and the depletion of monocytes/macrophages by clodronate treatment. We show that peritoneal macrophages appear in op/op((-/-)) mice after LPS stimulation and exhibit the same Ig gene rearrangement (VH11) that is often found in B-1 cells. These results strongly suggest that op/op((-/-)) peritoneal macrophages are B-1CDP. Similarly, the LPS-induced increase in the macrophage population was observed even following monocyte/macrophage depletion by clodronate. After monocyte/macrophage depletion by clodronate, LPS-elicited macrophages were observed in BALB/Xid mice only following the transfer of B-1 cells. Based on these data, we confirmed that B-1 cell differentiation into phagocytes also occurs in vivo. in conclusion, the results strongly suggest that B-1 cell derived phagocytes are a component of the LPS-elicited peritoneal macrophage population. |
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Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation?The inflammatory response is driven by signals that recruit and elicit immune cells to areas of tissue damage or infection. the concept of a mononuclear phagocyte system postulates that monocytes circulating in the bloodstream are recruited to inflamed tissues where they give rise to macrophages. A recent publication demonstrated that the large increase in the macrophages observed during infection was the result of the multiplication of these cells rather than the recruitment of blood monocytes. We demonstrated previously that B-1 cells undergo differentiation to acquire a mononuclear phagocyte phenotype in vitro (B-1CDP), and we propose that B-1 cells could be an alternative origin for peritoneal macrophages. A number of recent studies that describe the phagocytic and microbicidal activity of B-1 cells in vitro and in vivo support this hypothesis. Based on these findings, we further investigated the differentiation of B-1 cells into phagocytes in vivo in response to LPS-induced inflammation. Therefore, we investigated the role of B-1 cells in the composition of the peritoneal macrophage population after LPS stimulation using osteopetrotic mice, BALB/Xid mice and the depletion of monocytes/macrophages by clodronate treatment. We show that peritoneal macrophages appear in op/op((-/-)) mice after LPS stimulation and exhibit the same Ig gene rearrangement (VH11) that is often found in B-1 cells. These results strongly suggest that op/op((-/-)) peritoneal macrophages are B-1CDP. Similarly, the LPS-induced increase in the macrophage population was observed even following monocyte/macrophage depletion by clodronate. After monocyte/macrophage depletion by clodronate, LPS-elicited macrophages were observed in BALB/Xid mice only following the transfer of B-1 cells. Based on these data, we confirmed that B-1 cell differentiation into phagocytes also occurs in vivo. in conclusion, the results strongly suggest that B-1 cell derived phagocytes are a component of the LPS-elicited peritoneal macrophage population.Universidade Federal de São Paulo, UNIFESP, Discipline Immunol, Dept Microbiol Immunol & Parasitol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biophys, São Paulo, BrazilUniv Estadual Paulista, Lab Mol & Cellular Biol, UNIP, São Paulo, BrazilUniversidade Federal de São Paulo, UNIFESP, Discipline Immunol, Dept Microbiol Immunol & Parasitol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biophys, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)FAPESP: 2002/01354-6FAPESP: 2008/55526-9Public Library ScienceUniversidade Federal de São Paulo (UNIFESP)Univ Estadual PaulistaPopi, Ana Flavia [UNIFESP]Osugui, Lika [UNIFESP]Perez, Katia Regina [UNIFESP]Longo-Maugeri, Ieda Maria [UNIFESP]Mariano, Mario [UNIFESP]2016-01-24T14:26:59Z2016-01-24T14:26:59Z2012-03-30info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion12application/pdfhttp://dx.doi.org/10.1371/journal.pone.0034570Plos One. San Francisco: Public Library Science, v. 7, n. 3, 12 p., 2012.10.1371/journal.pone.0034570WOS000305339100169.pdf1932-6203http://repositorio.unifesp.br/handle/11600/34721WOS:000305339100169engPlos Oneinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T11:23:11Zoai:repositorio.unifesp.br/:11600/34721Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T11:23:11Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation? |
title |
Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation? |
spellingShingle |
Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation? Popi, Ana Flavia [UNIFESP] |
title_short |
Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation? |
title_full |
Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation? |
title_fullStr |
Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation? |
title_full_unstemmed |
Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation? |
title_sort |
Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation? |
author |
Popi, Ana Flavia [UNIFESP] |
author_facet |
Popi, Ana Flavia [UNIFESP] Osugui, Lika [UNIFESP] Perez, Katia Regina [UNIFESP] Longo-Maugeri, Ieda Maria [UNIFESP] Mariano, Mario [UNIFESP] |
author_role |
author |
author2 |
Osugui, Lika [UNIFESP] Perez, Katia Regina [UNIFESP] Longo-Maugeri, Ieda Maria [UNIFESP] Mariano, Mario [UNIFESP] |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Univ Estadual Paulista |
dc.contributor.author.fl_str_mv |
Popi, Ana Flavia [UNIFESP] Osugui, Lika [UNIFESP] Perez, Katia Regina [UNIFESP] Longo-Maugeri, Ieda Maria [UNIFESP] Mariano, Mario [UNIFESP] |
description |
The inflammatory response is driven by signals that recruit and elicit immune cells to areas of tissue damage or infection. the concept of a mononuclear phagocyte system postulates that monocytes circulating in the bloodstream are recruited to inflamed tissues where they give rise to macrophages. A recent publication demonstrated that the large increase in the macrophages observed during infection was the result of the multiplication of these cells rather than the recruitment of blood monocytes. We demonstrated previously that B-1 cells undergo differentiation to acquire a mononuclear phagocyte phenotype in vitro (B-1CDP), and we propose that B-1 cells could be an alternative origin for peritoneal macrophages. A number of recent studies that describe the phagocytic and microbicidal activity of B-1 cells in vitro and in vivo support this hypothesis. Based on these findings, we further investigated the differentiation of B-1 cells into phagocytes in vivo in response to LPS-induced inflammation. Therefore, we investigated the role of B-1 cells in the composition of the peritoneal macrophage population after LPS stimulation using osteopetrotic mice, BALB/Xid mice and the depletion of monocytes/macrophages by clodronate treatment. We show that peritoneal macrophages appear in op/op((-/-)) mice after LPS stimulation and exhibit the same Ig gene rearrangement (VH11) that is often found in B-1 cells. These results strongly suggest that op/op((-/-)) peritoneal macrophages are B-1CDP. Similarly, the LPS-induced increase in the macrophage population was observed even following monocyte/macrophage depletion by clodronate. After monocyte/macrophage depletion by clodronate, LPS-elicited macrophages were observed in BALB/Xid mice only following the transfer of B-1 cells. Based on these data, we confirmed that B-1 cell differentiation into phagocytes also occurs in vivo. in conclusion, the results strongly suggest that B-1 cell derived phagocytes are a component of the LPS-elicited peritoneal macrophage population. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-03-30 2016-01-24T14:26:59Z 2016-01-24T14:26:59Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1371/journal.pone.0034570 Plos One. San Francisco: Public Library Science, v. 7, n. 3, 12 p., 2012. 10.1371/journal.pone.0034570 WOS000305339100169.pdf 1932-6203 http://repositorio.unifesp.br/handle/11600/34721 WOS:000305339100169 |
url |
http://dx.doi.org/10.1371/journal.pone.0034570 http://repositorio.unifesp.br/handle/11600/34721 |
identifier_str_mv |
Plos One. San Francisco: Public Library Science, v. 7, n. 3, 12 p., 2012. 10.1371/journal.pone.0034570 WOS000305339100169.pdf 1932-6203 WOS:000305339100169 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Plos One |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
12 application/pdf |
dc.publisher.none.fl_str_mv |
Public Library Science |
publisher.none.fl_str_mv |
Public Library Science |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268436151271424 |