Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
Autor(a) principal: | |
---|---|
Data de Publicação: | 2009 |
Outros Autores: | , , , , , , , |
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 |
id |
UFSP_745c5ca168e2b4a514fc1f6cdef74637 |
---|---|
oai_identifier_str |
oai:repositorio.unifesp.br/:11600/31955 |
network_acronym_str |
UFSP |
network_name_str |
Repositório Institucional da UNIFESP |
repository_id_str |
3465 |
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 |
_version_ |
1814268398137245696 |