Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.bbrep.2022.101383 http://hdl.handle.net/11449/247903 |
Resumo: | Understanding macrophage biology can improve comprehension of diverse biological processes and provide insights into novel therapeutic immunomodulatory strategies. Due to limited yield and technical difficulty in isolating primary macrophages, in vitro studies commonly use monocytes as precursor cells. Monocytic cell lines are a virtually unlimited source of macrophage precursors and two of the most frequently used cell lines are THP-1 and U937. Besides a great variability in macrophage differentiation protocols there is scarce information on possible differences in the biological responses of these cell lines. In this study, we used a standardized differentiation protocol using PMA and compared the response of macrophages derived from THP-1 and U937 cells to M1-and M2-polarizing conditions. THP-1-derived macrophages are more responsive to M1 stimuli and skewed towards M1 phenotype, whereas U937-derived macrophages were more responsive to M2 stimuli and skewed towards M2 phenotype. THP-1-derived macrophages also had greater production of ROS and phagocytic activity. Under M1-polarizing conditions, macrophages derived from both THP-1 and U937 reduced phagocytosis activity and the increased production of ROS. This information should be considered to make an informed choice on the cell line used as in vitro macrophage model, according to the experimental goals and biological context. |
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Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studiesGene expressionMacrophagePhenotypeTHP-1 cellsU937 cellsUnderstanding macrophage biology can improve comprehension of diverse biological processes and provide insights into novel therapeutic immunomodulatory strategies. Due to limited yield and technical difficulty in isolating primary macrophages, in vitro studies commonly use monocytes as precursor cells. Monocytic cell lines are a virtually unlimited source of macrophage precursors and two of the most frequently used cell lines are THP-1 and U937. Besides a great variability in macrophage differentiation protocols there is scarce information on possible differences in the biological responses of these cell lines. In this study, we used a standardized differentiation protocol using PMA and compared the response of macrophages derived from THP-1 and U937 cells to M1-and M2-polarizing conditions. THP-1-derived macrophages are more responsive to M1 stimuli and skewed towards M1 phenotype, whereas U937-derived macrophages were more responsive to M2 stimuli and skewed towards M2 phenotype. THP-1-derived macrophages also had greater production of ROS and phagocytic activity. Under M1-polarizing conditions, macrophages derived from both THP-1 and U937 reduced phagocytosis activity and the increased production of ROS. This information should be considered to make an informed choice on the cell line used as in vitro macrophage model, according to the experimental goals and biological context.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Diagnosis and Surgery School of Dentistry at Araraquara São Paulo State University (UNESP), SPDepartment of Periodontics and Oral Medicine School of Dentistry University of MichiganDepartment of Diagnosis and Surgery School of Dentistry at Araraquara São Paulo State University (UNESP), SPFAPESP: 2018/24240-4Universidade Estadual Paulista (UNESP)University of MichiganNascimento, Camyla Rodrigues [UNESP]Rodrigues Fernandes, Natalie Ap [UNESP]Gonzalez Maldonado, Laura Andrea [UNESP]Rossa Junior, Carlos [UNESP]2023-07-29T13:29:02Z2023-07-29T13:29:02Z2022-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.bbrep.2022.101383Biochemistry and Biophysics Reports, v. 32.2405-5808http://hdl.handle.net/11449/24790310.1016/j.bbrep.2022.1013832-s2.0-85142156649Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiochemistry and Biophysics Reportsinfo:eu-repo/semantics/openAccess2024-09-26T15:22:12Zoai:repositorio.unesp.br:11449/247903Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-26T15:22:12Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies |
title |
Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies |
spellingShingle |
Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies Nascimento, Camyla Rodrigues [UNESP] Gene expression Macrophage Phenotype THP-1 cells U937 cells |
title_short |
Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies |
title_full |
Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies |
title_fullStr |
Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies |
title_full_unstemmed |
Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies |
title_sort |
Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies |
author |
Nascimento, Camyla Rodrigues [UNESP] |
author_facet |
Nascimento, Camyla Rodrigues [UNESP] Rodrigues Fernandes, Natalie Ap [UNESP] Gonzalez Maldonado, Laura Andrea [UNESP] Rossa Junior, Carlos [UNESP] |
author_role |
author |
author2 |
Rodrigues Fernandes, Natalie Ap [UNESP] Gonzalez Maldonado, Laura Andrea [UNESP] Rossa Junior, Carlos [UNESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) University of Michigan |
dc.contributor.author.fl_str_mv |
Nascimento, Camyla Rodrigues [UNESP] Rodrigues Fernandes, Natalie Ap [UNESP] Gonzalez Maldonado, Laura Andrea [UNESP] Rossa Junior, Carlos [UNESP] |
dc.subject.por.fl_str_mv |
Gene expression Macrophage Phenotype THP-1 cells U937 cells |
topic |
Gene expression Macrophage Phenotype THP-1 cells U937 cells |
description |
Understanding macrophage biology can improve comprehension of diverse biological processes and provide insights into novel therapeutic immunomodulatory strategies. Due to limited yield and technical difficulty in isolating primary macrophages, in vitro studies commonly use monocytes as precursor cells. Monocytic cell lines are a virtually unlimited source of macrophage precursors and two of the most frequently used cell lines are THP-1 and U937. Besides a great variability in macrophage differentiation protocols there is scarce information on possible differences in the biological responses of these cell lines. In this study, we used a standardized differentiation protocol using PMA and compared the response of macrophages derived from THP-1 and U937 cells to M1-and M2-polarizing conditions. THP-1-derived macrophages are more responsive to M1 stimuli and skewed towards M1 phenotype, whereas U937-derived macrophages were more responsive to M2 stimuli and skewed towards M2 phenotype. THP-1-derived macrophages also had greater production of ROS and phagocytic activity. Under M1-polarizing conditions, macrophages derived from both THP-1 and U937 reduced phagocytosis activity and the increased production of ROS. This information should be considered to make an informed choice on the cell line used as in vitro macrophage model, according to the experimental goals and biological context. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-12-01 2023-07-29T13:29:02Z 2023-07-29T13:29:02Z |
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.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.bbrep.2022.101383 Biochemistry and Biophysics Reports, v. 32. 2405-5808 http://hdl.handle.net/11449/247903 10.1016/j.bbrep.2022.101383 2-s2.0-85142156649 |
url |
http://dx.doi.org/10.1016/j.bbrep.2022.101383 http://hdl.handle.net/11449/247903 |
identifier_str_mv |
Biochemistry and Biophysics Reports, v. 32. 2405-5808 10.1016/j.bbrep.2022.101383 2-s2.0-85142156649 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Biochemistry and Biophysics Reports |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1813546503238582272 |