Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da FIOCRUZ (ARCA) |
Texto Completo: | https://www.arca.fiocruz.br/handle/icict/23531 |
Resumo: | 2021-01-01 |
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David, Bruna AraujoRezende, Rafael MachadoAntunes, Maísa MotaSantos, Mônica MoraisLopes, Maria Alice FreitasDiniz, Ariane BarrosPereira, Rafaela Vaz SousaMarchesi, Sarah CozzerAlvarenga, Débora MoreiraNakagaki, Brenda NaemiAraújo, Alan MoreiraReis, Daniela Silva dosRocha, Renata MontiMarques, Pedro EliasLee, Woo-YongDeniset, JustinLiew, Pei XiongRubino, StephenCox, LauraPinho, VanessaCunha, Thiago MattarFernandes, Gabriel RochaOliveira, André GustavoTeixeira, Mauro MartinsKubes, PaulMenezes, Gustavo Batista2017-12-06T18:43:34Z2017-12-06T18:43:34Z2016DAVID, Bruna Araujo et al. Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice. Gastroenterology. v. 151, n. 6, p. 1176-1191, 20160016-5085https://www.arca.fiocruz.br/handle/icict/2353110.1053/j.gastro.2016.08.024engElsevier Inc.CyTOFDCCyTOFDCLiver DevelopmentMouse ModelCombination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Miceinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2021-01-01Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilHarvard Medical School, Brigham and Women’s Hospital. Ann Romney Center for Neurologic Diseases. Boston, MA, United States of America.Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais. Belo Horizonte, MG, BrazilUniversity of Calgary. Alberta, CanadaUniversity of Calgary. Alberta, CanadaUniversity of Calgary. Alberta, CanadaHarvard Medical School, Brigham and Women’s Hospital. Ann Romney Center for Neurologic Diseases. Boston, MA, United States of America.Harvard Medical School, Brigham and Women’s Hospital. Ann Romney Center for Neurologic Diseases. Boston, MA, United States of America.Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Laboratório de Resolução de Inflamação. Belo Horizonte, MG, BrazilUniversidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. São Paulo, SP, BrazilFundação Oswaldo Cruz. Instituto René Rachou. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, Brazil/Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Fisiologia. Belo Horizonte, MG, BrazilUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais. Belo Horizonte, MG, BrazilUniversity of Calgary. Alberta, CanadaUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Morfologia. Centro de Biologia Gastrointestinal. Belo Horizonte, MG, BrazilBACKGROUND & AIMS: Resident macrophages are derived from yolk sac precursors and seed the liver during embryogenesis. Native cells may be replaced by bone marrow precursors during extensive injuries, irradiation, and infections. We investigated the liver populations of myeloid immune cells and their location, as well as the dynamics of phagocyte repopulation after full depletion. The effects on liver function due to the substitution of original phagocytes by bone marrow-derived surrogates were also examined. METHODS: We collected and analyzed liver tissues from C57BL/6 (control), LysM-EGFP, B6 ACTb-EGFP, CCR2-/-, CD11c-EYFP, CD11c-EYFP-DTR, germ-free mice, CX3CR1gfp/gfp, CX3CR1gpf/wt, and CX3CR1-DTR-EYFP. Liver nonparenchymal cells were immunophenotyped using mass cytometry and gene expression analyses. Kupffer and dendritic cells were depleted from mice by administration of clodronate, and their location and phenotype were examined using intravital microscopy and time-of-flight mass cytometry. Mice were given acetaminophen gavage or intravenous injections of fluorescently labeled Escherichia coli, blood samples were collected and analyzed, and liver function was evaluated. We assessed cytokine profiles of liver tissues using a multiplexed array. RESULTS: Using mass cytometry and gene expression analyses, we identified 2 populations of hepatic macrophages and 2 populations of monocytes. We also identified 4 populations of dendritic cells and 1 population of basophils. After selective depletion of liver phagocytes, intravascular myeloid precursors began to differentiate into macrophages and dendritic cells; dendritic cells migrated out of sinusoids, after a delay, via the chemokine CX3CL1. The cell distribution returned to normal in 2 weeks, but the repopulated livers were unable to fully respond to drug-induced injury or clear bacteria for at least 1 month. This defect was associated with increased levels of inflammatory cytokines, and dexamethasone accelerated the repopulation of liver phagocytes. CONCLUSIONS: In studies of hepatic phagocyte depletion in mice, we found that myeloid precursors can differentiate into liver macrophages and dendritic cells, which each localize to distinct tissue compartments. During replenishment, macrophages acquire the ability to respond appropriately to hepatic injury and to remove bacteria from the blood stream.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; charset=utf-83082https://www.arca.fiocruz.br/bitstream/icict/23531/1/license.txt9193a7c197bc67acd023525e72a03240MD51ORIGINALCombination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice.pdfCombination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in 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dc.title.pt_BR.fl_str_mv |
Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice |
title |
Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice |
spellingShingle |
Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice David, Bruna Araujo CyTOF DC CyTOF DC Liver Development Mouse Model |
title_short |
Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice |
title_full |
Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice |
title_fullStr |
Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice |
title_full_unstemmed |
Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice |
title_sort |
Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice |
author |
David, Bruna Araujo |
author_facet |
David, Bruna Araujo Rezende, Rafael Machado Antunes, Maísa Mota Santos, Mônica Morais Lopes, Maria Alice Freitas Diniz, Ariane Barros Pereira, Rafaela Vaz Sousa Marchesi, Sarah Cozzer Alvarenga, Débora Moreira Nakagaki, Brenda Naemi Araújo, Alan Moreira Reis, Daniela Silva dos Rocha, Renata Monti Marques, Pedro Elias Lee, Woo-Yong Deniset, Justin Liew, Pei Xiong Rubino, Stephen Cox, Laura Pinho, Vanessa Cunha, Thiago Mattar Fernandes, Gabriel Rocha Oliveira, André Gustavo Teixeira, Mauro Martins Kubes, Paul Menezes, Gustavo Batista |
author_role |
author |
author2 |
Rezende, Rafael Machado Antunes, Maísa Mota Santos, Mônica Morais Lopes, Maria Alice Freitas Diniz, Ariane Barros Pereira, Rafaela Vaz Sousa Marchesi, Sarah Cozzer Alvarenga, Débora Moreira Nakagaki, Brenda Naemi Araújo, Alan Moreira Reis, Daniela Silva dos Rocha, Renata Monti Marques, Pedro Elias Lee, Woo-Yong Deniset, Justin Liew, Pei Xiong Rubino, Stephen Cox, Laura Pinho, Vanessa Cunha, Thiago Mattar Fernandes, Gabriel Rocha Oliveira, André Gustavo Teixeira, Mauro Martins Kubes, Paul Menezes, Gustavo Batista |
author2_role |
author author author author author author author author author author author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
David, Bruna Araujo Rezende, Rafael Machado Antunes, Maísa Mota Santos, Mônica Morais Lopes, Maria Alice Freitas Diniz, Ariane Barros Pereira, Rafaela Vaz Sousa Marchesi, Sarah Cozzer Alvarenga, Débora Moreira Nakagaki, Brenda Naemi Araújo, Alan Moreira Reis, Daniela Silva dos Rocha, Renata Monti Marques, Pedro Elias Lee, Woo-Yong Deniset, Justin Liew, Pei Xiong Rubino, Stephen Cox, Laura Pinho, Vanessa Cunha, Thiago Mattar Fernandes, Gabriel Rocha Oliveira, André Gustavo Teixeira, Mauro Martins Kubes, Paul Menezes, Gustavo Batista |
dc.subject.other.pt_BR.fl_str_mv |
CyTOF DC |
topic |
CyTOF DC CyTOF DC Liver Development Mouse Model |
dc.subject.en.pt_BR.fl_str_mv |
CyTOF DC Liver Development Mouse Model |
description |
2021-01-01 |
publishDate |
2016 |
dc.date.issued.fl_str_mv |
2016 |
dc.date.accessioned.fl_str_mv |
2017-12-06T18:43:34Z |
dc.date.available.fl_str_mv |
2017-12-06T18:43:34Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
DAVID, Bruna Araujo et al. Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice. Gastroenterology. v. 151, n. 6, p. 1176-1191, 2016 |
dc.identifier.uri.fl_str_mv |
https://www.arca.fiocruz.br/handle/icict/23531 |
dc.identifier.issn.pt_BR.fl_str_mv |
0016-5085 |
dc.identifier.doi.none.fl_str_mv |
10.1053/j.gastro.2016.08.024 |
identifier_str_mv |
DAVID, Bruna Araujo et al. Combination of Mass Cytometry and Imaging Analysis Reveals Origin, Location, and Functional Repopulation of Liver Myeloid Cells in Mice. Gastroenterology. v. 151, n. 6, p. 1176-1191, 2016 0016-5085 10.1053/j.gastro.2016.08.024 |
url |
https://www.arca.fiocruz.br/handle/icict/23531 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Elsevier Inc. |
publisher.none.fl_str_mv |
Elsevier Inc. |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da FIOCRUZ (ARCA) instname:Fundação Oswaldo Cruz (FIOCRUZ) instacron:FIOCRUZ |
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Fundação Oswaldo Cruz (FIOCRUZ) |
instacron_str |
FIOCRUZ |
institution |
FIOCRUZ |
reponame_str |
Repositório Institucional da FIOCRUZ (ARCA) |
collection |
Repositório Institucional da FIOCRUZ (ARCA) |
bitstream.url.fl_str_mv |
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