Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model

Detalhes bibliográficos
Autor(a) principal: Semedo, Patricia [UNIFESP]
Data de Publicação: 2009
Outros Autores: Correa-Costa, Matheus [UNIFESP], Cenedeze, Marcos Antonio [UNIFESP], Malheiros, Denise Maria Avancini Costa, Reis, Marlene Antonia dos, Shimizu, Maria Heloisa, Seguro, Antonio Carlos, Pacheco-Silva, Alvaro [UNIFESP], Câmara, Niels Olsen Saraiva [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1002/stem.214
http://repositorio.unifesp.br/handle/11600/31955
Resumo: Mesenchymal stem cells (MSCs) have regenerative properties in acute kidney injury, but their role in chronic kidney diseases is still unknown. More specifically, it is not known whether MSCs halt fibrosis. the purpose of this work was to investigate the role of MSCs in fibrogenesis using a model of chronic renal failure. MSCs were obtained from the tibias and femurs of male Wistar-EPM rats. Female Wistar rats were subjected to the remnant model, and 2 vertical bar x vertical bar 10(5) MSCs were intravenously administrated to each rat every other week for 8 weeks or only once and followed for 12 weeks. SRY gene expression was observed in female rats treated with male MSCs, and immune localization of CD73(+)CD90(+) cells at 8 weeks was also assessed. Serum and urine analyses showed an amelioration of functional parameters in MSC-treated animals at 8 weeks, but not at 12 weeks. Masson's trichrome and Sirius red staining demonstrated reduced levels of fibrosis in MSC-treated animals. These results were corroborated by reduced vimentin, type I collagen, transforming growth factor beta, fibroblast specific protein 1 (FSP-1), monocyte chemoattractant protein 1, and Smad3 mRNA expression and alpha smooth muscle actin and FSP-1 protein expression. Renal interleukin (IL)-6 and tumor necrosis factor alpha mRNA expression levels were significantly decreased after MSC treatment, whereas IL-4 and IL-10 expression levels were increased. All serum cytokine expression levels were decreased in MSC-treated animals. Taken together, these results suggested that MSC therapy can indeed modulate the inflammatory response that follows the initial phase of a chronic renal injury. the immunosuppressive and remodeling properties of MSCs may be involved in the decreased fibrosis in the kidney. STEM CELLS 2009;27:3063-3073
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spelling Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney ModelMesenchymal stem cellIschemia-reperfusion injuryFibrosisChronic renal failureKidney fibrosisMesenchymal stem cells (MSCs) have regenerative properties in acute kidney injury, but their role in chronic kidney diseases is still unknown. More specifically, it is not known whether MSCs halt fibrosis. the purpose of this work was to investigate the role of MSCs in fibrogenesis using a model of chronic renal failure. MSCs were obtained from the tibias and femurs of male Wistar-EPM rats. Female Wistar rats were subjected to the remnant model, and 2 vertical bar x vertical bar 10(5) MSCs were intravenously administrated to each rat every other week for 8 weeks or only once and followed for 12 weeks. SRY gene expression was observed in female rats treated with male MSCs, and immune localization of CD73(+)CD90(+) cells at 8 weeks was also assessed. Serum and urine analyses showed an amelioration of functional parameters in MSC-treated animals at 8 weeks, but not at 12 weeks. Masson's trichrome and Sirius red staining demonstrated reduced levels of fibrosis in MSC-treated animals. These results were corroborated by reduced vimentin, type I collagen, transforming growth factor beta, fibroblast specific protein 1 (FSP-1), monocyte chemoattractant protein 1, and Smad3 mRNA expression and alpha smooth muscle actin and FSP-1 protein expression. Renal interleukin (IL)-6 and tumor necrosis factor alpha mRNA expression levels were significantly decreased after MSC treatment, whereas IL-4 and IL-10 expression levels were increased. All serum cytokine expression levels were decreased in MSC-treated animals. Taken together, these results suggested that MSC therapy can indeed modulate the inflammatory response that follows the initial phase of a chronic renal injury. the immunosuppressive and remodeling properties of MSCs may be involved in the decreased fibrosis in the kidney. STEM CELLS 2009;27:3063-3073Univ São Paulo, Dept Immunol, Inst Biomed Sci 4, Lab Transplantat Immunobiol, BR-05508900 São Paulo, BrazilUniversidade Federal de São Paulo, Div Nephrol, Dept Med, São Paulo, BrazilUniv São Paulo, Dept Pathol, BR-05508900 São Paulo, BrazilTriangulo Mineiro Med Sch, Gen Pathol Div, Belo Horizonte, MG, BrazilUniv São Paulo, Sch Med, Dept Nephrol, BR-05508900 São Paulo, BrazilAlbert Einstein Hosp, IIEP, São Paulo, BrazilUniversidade Federal de São Paulo, Div Nephrol, Dept Med, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Brazilian Council of Scientific and Technologic DevelopmentMS/DECITFAPESP: 04/08226-9FAPESP: 06/0620-5FAPESP: 07/07139-3Brazilian Council of Scientific and Technologic Development: 573815/2008-9-CNPqAlphamed PressUniversidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Triangulo Mineiro Med SchAlbert Einstein HospSemedo, Patricia [UNIFESP]Correa-Costa, Matheus [UNIFESP]Cenedeze, Marcos Antonio [UNIFESP]Malheiros, Denise Maria Avancini CostaReis, Marlene Antonia dosShimizu, Maria HeloisaSeguro, Antonio CarlosPacheco-Silva, Alvaro [UNIFESP]Câmara, Niels Olsen Saraiva [UNIFESP]2016-01-24T13:58:55Z2016-01-24T13:58:55Z2009-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion3063-3073http://dx.doi.org/10.1002/stem.214Stem Cells. Durham: Alphamed Press, v. 27, n. 12, p. 3063-3073, 2009.10.1002/stem.2141066-5099http://repositorio.unifesp.br/handle/11600/31955WOS:000273569800019engStem Cellsinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T11:58:55Zoai:repositorio.unifesp.br/:11600/31955Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-01-24T11:58:55Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
title Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
spellingShingle Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
Semedo, Patricia [UNIFESP]
Mesenchymal stem cell
Ischemia-reperfusion injury
Fibrosis
Chronic renal failure
Kidney fibrosis
title_short Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
title_full Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
title_fullStr Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
title_full_unstemmed Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
title_sort Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
author Semedo, Patricia [UNIFESP]
author_facet Semedo, Patricia [UNIFESP]
Correa-Costa, Matheus [UNIFESP]
Cenedeze, Marcos Antonio [UNIFESP]
Malheiros, Denise Maria Avancini Costa
Reis, Marlene Antonia dos
Shimizu, Maria Heloisa
Seguro, Antonio Carlos
Pacheco-Silva, Alvaro [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
author_role author
author2 Correa-Costa, Matheus [UNIFESP]
Cenedeze, Marcos Antonio [UNIFESP]
Malheiros, Denise Maria Avancini Costa
Reis, Marlene Antonia dos
Shimizu, Maria Heloisa
Seguro, Antonio Carlos
Pacheco-Silva, Alvaro [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
Triangulo Mineiro Med Sch
Albert Einstein Hosp
dc.contributor.author.fl_str_mv Semedo, Patricia [UNIFESP]
Correa-Costa, Matheus [UNIFESP]
Cenedeze, Marcos Antonio [UNIFESP]
Malheiros, Denise Maria Avancini Costa
Reis, Marlene Antonia dos
Shimizu, Maria Heloisa
Seguro, Antonio Carlos
Pacheco-Silva, Alvaro [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
dc.subject.por.fl_str_mv Mesenchymal stem cell
Ischemia-reperfusion injury
Fibrosis
Chronic renal failure
Kidney fibrosis
topic Mesenchymal stem cell
Ischemia-reperfusion injury
Fibrosis
Chronic renal failure
Kidney fibrosis
description Mesenchymal stem cells (MSCs) have regenerative properties in acute kidney injury, but their role in chronic kidney diseases is still unknown. More specifically, it is not known whether MSCs halt fibrosis. the purpose of this work was to investigate the role of MSCs in fibrogenesis using a model of chronic renal failure. MSCs were obtained from the tibias and femurs of male Wistar-EPM rats. Female Wistar rats were subjected to the remnant model, and 2 vertical bar x vertical bar 10(5) MSCs were intravenously administrated to each rat every other week for 8 weeks or only once and followed for 12 weeks. SRY gene expression was observed in female rats treated with male MSCs, and immune localization of CD73(+)CD90(+) cells at 8 weeks was also assessed. Serum and urine analyses showed an amelioration of functional parameters in MSC-treated animals at 8 weeks, but not at 12 weeks. Masson's trichrome and Sirius red staining demonstrated reduced levels of fibrosis in MSC-treated animals. These results were corroborated by reduced vimentin, type I collagen, transforming growth factor beta, fibroblast specific protein 1 (FSP-1), monocyte chemoattractant protein 1, and Smad3 mRNA expression and alpha smooth muscle actin and FSP-1 protein expression. Renal interleukin (IL)-6 and tumor necrosis factor alpha mRNA expression levels were significantly decreased after MSC treatment, whereas IL-4 and IL-10 expression levels were increased. All serum cytokine expression levels were decreased in MSC-treated animals. Taken together, these results suggested that MSC therapy can indeed modulate the inflammatory response that follows the initial phase of a chronic renal injury. the immunosuppressive and remodeling properties of MSCs may be involved in the decreased fibrosis in the kidney. STEM CELLS 2009;27:3063-3073
publishDate 2009
dc.date.none.fl_str_mv 2009-12-01
2016-01-24T13:58:55Z
2016-01-24T13:58:55Z
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/10.1002/stem.214
Stem Cells. Durham: Alphamed Press, v. 27, n. 12, p. 3063-3073, 2009.
10.1002/stem.214
1066-5099
http://repositorio.unifesp.br/handle/11600/31955
WOS:000273569800019
url http://dx.doi.org/10.1002/stem.214
http://repositorio.unifesp.br/handle/11600/31955
identifier_str_mv Stem Cells. Durham: Alphamed Press, v. 27, n. 12, p. 3063-3073, 2009.
10.1002/stem.214
1066-5099
WOS:000273569800019
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Stem Cells
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 3063-3073
dc.publisher.none.fl_str_mv Alphamed Press
publisher.none.fl_str_mv Alphamed Press
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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