Could a B-1 Cell Derived Phagocyte Be One of the Peritoneal Macrophages during LPS-Driven Inflammation?

Detalhes bibliográficos
Autor(a) principal: Popi, Ana Flavia [UNIFESP]
Data de Publicação: 2012
Outros Autores: Osugui, Lika [UNIFESP], Perez, Katia Regina [UNIFESP], Longo-Maugeri, Ieda Maria [UNIFESP], Mariano, Mario [UNIFESP]
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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spelling 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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