Comparison of monocytic cell lines U937 and THP-1 as macrophage models for in vitro studies

Detalhes bibliográficos
Autor(a) principal: Nascimento, Camyla Rodrigues [UNESP]
Data de Publicação: 2022
Outros Autores: Rodrigues Fernandes, Natalie Ap [UNESP], Gonzalez Maldonado, Laura Andrea [UNESP], Rossa Junior, Carlos [UNESP]
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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spelling 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
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