Expanded endothelial progenitor cells mitigate lung injury in septic mice

Detalhes bibliográficos
Autor(a) principal: Güldner, Andreas
Data de Publicação: 2015
Outros Autores: Maron-Gutierrez, Tatiana, Abreu, Soraia Carvalho, Xisto, Debora Gonçalves, Senegaglia, Alexandra Cristina, Barcelos, Patty Rose da Silva, Silva, Johnatas Dutra, Brofman, Paulo, Abreu, Marcelo Gama de, Rocco, Patricia Rieken Macedo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da FIOCRUZ (ARCA)
DOI: 10.1186/s13287-015-0226-7
Texto Completo: https://www.arca.fiocruz.br/handle/icict/13246
Resumo: Technische Universität Dresden. University Hospital Dresden. Department of Anesthesiology and Intensive Care Medicine. Dredesm Germany / Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Biofísica Carlos Chagas Filho (IBCCF). Laboratório de Investigação Pulmonar. Rio de Janeiro, RJ, Brasil.
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spelling Güldner, AndreasMaron-Gutierrez, TatianaAbreu, Soraia CarvalhoXisto, Debora GonçalvesSenegaglia, Alexandra CristinaBarcelos, Patty Rose da SilvaSilva, Johnatas DutraBrofman, PauloAbreu, Marcelo Gama deRocco, Patricia Rieken Macedo2016-03-22T17:10:21Z2016-03-22T17:10:21Z2015GÜLDNER, Andreas; et al. Expanded endothelial progenitor cells mitigate lung injury in septic mice. Stem Cell Research & Therapy, v.6:230, 8p, 2015.https://www.arca.fiocruz.br/handle/icict/1324610.1186/s13287-015-0226-71757-6512engBioMed CentralTerapias celularesSepsisInflammationGrowth factorsCell therapiesPeptídeos e Proteínas de Sinalização IntercelularInflamaçãoSepseExpanded endothelial progenitor cells mitigate lung injury in septic miceinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleTechnische Universität Dresden. University Hospital Dresden. Department of Anesthesiology and Intensive Care Medicine. Dredesm Germany / Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Biofísica Carlos Chagas Filho (IBCCF). Laboratório de Investigação Pulmonar. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Biofísica Carlos Chagas Filho (IBCCF). Laboratório de Investigação Pulmonar. Rio de Janeiro, RJ, Brasil / Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Imunofarmacologia. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Biofísica Carlos Chagas Filho (IBCCF). Laboratório de Investigação Pulmonar. Rio de Janeiro, RJ, BrasilUniversidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Biofísica Carlos Chagas Filho (IBCCF). Laboratório de Investigação Pulmonar. Rio de Janeiro, RJ, BrasilPontifícia Universidade Católica do Paraná. Centro de Tecnologia Celular. Curitiba, PR, Brasil.Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Biofísica Carlos Chagas Filho (IBCCF). Laboratório de Investigação Pulmonar. Rio de Janeiro, RJ, BrasilUniversidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Biofísica Carlos Chagas Filho (IBCCF). Laboratório de Investigação Pulmonar. Rio de Janeiro, RJ, BrasilPontifícia Universidade Católica do Paraná. Centro de Tecnologia Celular. Curitiba, PR, Brasil.Technische Universität Dresden. University Hospital Dresden. Department of Anesthesiology and Intensive Care Medicine. Dredesm Germany.Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Biofísica Carlos Chagas Filho (IBCCF). Laboratório de Investigação Pulmonar. Rio de Janeiro, RJ, Brasil.Endothelial progenitor cells (EPCs) improve survival and reduce organ failure in cecal ligation and puncture-induced sepsis; however, expanded EPCs may represent an even better approach for vascular repair. To date, no study has compared the effects of non-expanded EPCs (EPC-NEXP) with those of expanded EPCs (EPC-EXP) and mesenchymal stromal cells of human (MSC-HUMAN) and mouse (MSC-MICE) origin in experimental sepsis. One day after cecal ligation and puncture sepsis induction, BALB/c mice were randomized to receive saline, EPC-EXP, EPC-NEXP, MSC-HUMAN or MSC-MICE (1 × 105 ) intravenously. EPC-EXP, EPC-NEXP, MSC-HUMAN, and MSC-MICE displayed differences in phenotypic characterization. On days 1 and 3, cecal ligation and puncture mice showed decreased survival rate, and increased elastance, diffuse alveolar damage, and levels of interleukin (IL)-1β, IL-6, IL-10, tumor necrosis factor-α, vascular endothelial growth factor, and platelet-derived growth factor in lung tissue. EPC-EXP and MSC-HUMAN had reduced elastance, diffuse alveolar damage, and platelet-derived growth factor compared to no-cell treatment. Tumor necrosis factor-α levels decreased in the EPC-EXP, MSC-HUMAN, and MSC-MICE groups. IL-1β levels decreased in the EPC-EXP group, while IL-10 decreased in the MSC-MICE. IL-6 levels decreased both in the EPC-EXP and MSC-MICE groups. Vascular endothelial growth factor levels were reduced regardless of therapy. In conclusion, EPC-EXP and MSC-HUMAN yielded better lung function and reduced histologic damage in septic mice.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; charset=utf-82991https://www.arca.fiocruz.br/bitstream/icict/13246/1/license.txt5a560609d32a3863062d77ff32785d58MD51ORIGINALtataina_gutierrez_etal_IOC_2015.pdftataina_gutierrez_etal_IOC_2015.pdfapplication/pdf942633https://www.arca.fiocruz.br/bitstream/icict/13246/2/tataina_gutierrez_etal_IOC_2015.pdf816a2181c5a43c3038245cde47196e7aMD52TEXTtataina_gutierrez_etal_IOC_2015.pdf.txttataina_gutierrez_etal_IOC_2015.pdf.txtExtracted texttext/plain35832https://www.arca.fiocruz.br/bitstream/icict/13246/3/tataina_gutierrez_etal_IOC_2015.pdf.txt535b718c7f20da0525de3e0355389f91MD53icict/132462018-04-02 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dc.title.pt_BR.fl_str_mv Expanded endothelial progenitor cells mitigate lung injury in septic mice
title Expanded endothelial progenitor cells mitigate lung injury in septic mice
spellingShingle Expanded endothelial progenitor cells mitigate lung injury in septic mice
Güldner, Andreas
Terapias celulares
Sepsis
Inflammation
Growth factors
Cell therapies
Peptídeos e Proteínas de Sinalização Intercelular
Inflamação
Sepse
title_short Expanded endothelial progenitor cells mitigate lung injury in septic mice
title_full Expanded endothelial progenitor cells mitigate lung injury in septic mice
title_fullStr Expanded endothelial progenitor cells mitigate lung injury in septic mice
title_full_unstemmed Expanded endothelial progenitor cells mitigate lung injury in septic mice
title_sort Expanded endothelial progenitor cells mitigate lung injury in septic mice
author Güldner, Andreas
author_facet Güldner, Andreas
Maron-Gutierrez, Tatiana
Abreu, Soraia Carvalho
Xisto, Debora Gonçalves
Senegaglia, Alexandra Cristina
Barcelos, Patty Rose da Silva
Silva, Johnatas Dutra
Brofman, Paulo
Abreu, Marcelo Gama de
Rocco, Patricia Rieken Macedo
author_role author
author2 Maron-Gutierrez, Tatiana
Abreu, Soraia Carvalho
Xisto, Debora Gonçalves
Senegaglia, Alexandra Cristina
Barcelos, Patty Rose da Silva
Silva, Johnatas Dutra
Brofman, Paulo
Abreu, Marcelo Gama de
Rocco, Patricia Rieken Macedo
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Güldner, Andreas
Maron-Gutierrez, Tatiana
Abreu, Soraia Carvalho
Xisto, Debora Gonçalves
Senegaglia, Alexandra Cristina
Barcelos, Patty Rose da Silva
Silva, Johnatas Dutra
Brofman, Paulo
Abreu, Marcelo Gama de
Rocco, Patricia Rieken Macedo
dc.subject.other.pt_BR.fl_str_mv Terapias celulares
topic Terapias celulares
Sepsis
Inflammation
Growth factors
Cell therapies
Peptídeos e Proteínas de Sinalização Intercelular
Inflamação
Sepse
dc.subject.en.pt_BR.fl_str_mv Sepsis
Inflammation
Growth factors
Cell therapies
dc.subject.decs.pt_BR.fl_str_mv Peptídeos e Proteínas de Sinalização Intercelular
Inflamação
Sepse
description Technische Universität Dresden. University Hospital Dresden. Department of Anesthesiology and Intensive Care Medicine. Dredesm Germany / Universidade Federal do Rio de Janeiro. Centro de Ciências da Saúde. Instituto de Biofísica Carlos Chagas Filho (IBCCF). Laboratório de Investigação Pulmonar. Rio de Janeiro, RJ, Brasil.
publishDate 2015
dc.date.issued.fl_str_mv 2015
dc.date.accessioned.fl_str_mv 2016-03-22T17:10:21Z
dc.date.available.fl_str_mv 2016-03-22T17:10:21Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.citation.fl_str_mv GÜLDNER, Andreas; et al. Expanded endothelial progenitor cells mitigate lung injury in septic mice. Stem Cell Research & Therapy, v.6:230, 8p, 2015.
dc.identifier.uri.fl_str_mv https://www.arca.fiocruz.br/handle/icict/13246
dc.identifier.doi.none.fl_str_mv 10.1186/s13287-015-0226-7
dc.identifier.eissn.none.fl_str_mv 1757-6512
identifier_str_mv GÜLDNER, Andreas; et al. Expanded endothelial progenitor cells mitigate lung injury in septic mice. Stem Cell Research & Therapy, v.6:230, 8p, 2015.
10.1186/s13287-015-0226-7
1757-6512
url https://www.arca.fiocruz.br/handle/icict/13246
dc.language.iso.fl_str_mv eng
language eng
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dc.publisher.none.fl_str_mv BioMed Central
publisher.none.fl_str_mv BioMed Central
dc.source.none.fl_str_mv reponame:Repositório Institucional da FIOCRUZ (ARCA)
instname:Fundação Oswaldo Cruz (FIOCRUZ)
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