Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression

Detalhes bibliográficos
Autor(a) principal: Donizetti-Oliveira, Cassiano [UNIFESP]
Data de Publicação: 2012
Outros Autores: Semedo, Patricia [UNIFESP], Burgos-Silva, Marina [UNIFESP], Cenedeze, Marco Antonio [UNIFESP], Malheiros, Denise Maria Avancini Costa, Reis, Marlene A., 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/10.3727/096368911X623925
http://repositorio.unifesp.br/handle/11600/34404
Resumo: Adipose tissue-derived stem cells (ASCs) are an attractive source of stem cells with regenerative properties that are similar to those of bone marrow stem cells. Here, we analyze the role of ASCs in reducing the progression of kidney fibrosis. Progressive renal fibrosis was achieved by unilateral clamping of the renal pedicle in mice for 1 h; after that, the kidney was reperfused immediately. Four hours after the surgery, 2 x 10(5) ASCs were intraperitoneally administered, and mice were followed for 24 h posttreatment and then at some other time interval for the next 6 weeks. Also, animals were treated with 2 x 10(5) ASCs at 6 weeks after reperfusion and sacrificed 4 weeks later to study their effect when interstitial fibrosis is already present. At 24 h after reperfusion, ASC-treated animals showed reduced renal dysfunction and enhanced regenerative tubular processes. Renal mRNA expression of IL-6 and TNF was decreased in ASC-treated animals, whereas IL-4. IL-10, and HO-1 expression increased despite a lack of ASCs in the kidneys as determined by SRY analysis. As expected, untreated kidneys shrank at 6 weeks, whereas the kidneys of ASC-treated animals remained normal in size, showed less collagen deposition, and decreased staining for FSP-1, type I collagen, and Hypoxyprobe. the renal protection seen in ASC-treated animals was followed by reduced serum levels of TNF-alpha, KC, RANTES, and IL-1 alpha. Surprisingly, treatment with ASCs at 6 weeks, when animals already showed installed fibrosis, demonstrated amelioration of functional parameters, with less tissue fibrosis observed and reduced mRNA expression of type I collagen and vimentin. ASC therapy can improve functional parameters and reduce progression of renal fibrosis at early and later times after injury, mostly due to early modulation of the inflammatory response and to less hypoxia, thereby reducing the epithelial-mesenchymal transition.
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spelling Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease ProgressionAdipose-derived stem cellAcute kidney injuryIschemia-reperfusion injuryFibrosisInflammationAdipose tissue-derived stem cells (ASCs) are an attractive source of stem cells with regenerative properties that are similar to those of bone marrow stem cells. Here, we analyze the role of ASCs in reducing the progression of kidney fibrosis. Progressive renal fibrosis was achieved by unilateral clamping of the renal pedicle in mice for 1 h; after that, the kidney was reperfused immediately. Four hours after the surgery, 2 x 10(5) ASCs were intraperitoneally administered, and mice were followed for 24 h posttreatment and then at some other time interval for the next 6 weeks. Also, animals were treated with 2 x 10(5) ASCs at 6 weeks after reperfusion and sacrificed 4 weeks later to study their effect when interstitial fibrosis is already present. At 24 h after reperfusion, ASC-treated animals showed reduced renal dysfunction and enhanced regenerative tubular processes. Renal mRNA expression of IL-6 and TNF was decreased in ASC-treated animals, whereas IL-4. IL-10, and HO-1 expression increased despite a lack of ASCs in the kidneys as determined by SRY analysis. As expected, untreated kidneys shrank at 6 weeks, whereas the kidneys of ASC-treated animals remained normal in size, showed less collagen deposition, and decreased staining for FSP-1, type I collagen, and Hypoxyprobe. the renal protection seen in ASC-treated animals was followed by reduced serum levels of TNF-alpha, KC, RANTES, and IL-1 alpha. Surprisingly, treatment with ASCs at 6 weeks, when animals already showed installed fibrosis, demonstrated amelioration of functional parameters, with less tissue fibrosis observed and reduced mRNA expression of type I collagen and vimentin. ASC therapy can improve functional parameters and reduce progression of renal fibrosis at early and later times after injury, mostly due to early modulation of the inflammatory response and to less hypoxia, thereby reducing the epithelial-mesenchymal transition.Universidade Federal de São Paulo, Div Nephrol, Escola Paulista Med, Expt & Clin Immunol Lab, BR-04023900 São Paulo, BrazilUniv São Paulo, Dept Pathol, São Paulo, BrazilUniv Fed Triangulo Mineiro, Div Pathol, Uberaba, MG, BrazilUniv São Paulo, Dept Immunol, Lab Transplantat Immunobiol, São Paulo, BrazilUniversidade Federal de São Paulo, Div Nephrol, Escola Paulista Med, Expt & Clin Immunol Lab, BR-04023900 São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)DECIT/Ministerio do SaudeComplex Fluids INCTFAPESP: 09/13251-6FAPESP: 07/07139-3CNPq: 473844/2009-5Cognizant Communication CorpUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Univ Fed Triangulo MineiroDonizetti-Oliveira, Cassiano [UNIFESP]Semedo, Patricia [UNIFESP]Burgos-Silva, Marina [UNIFESP]Cenedeze, Marco Antonio [UNIFESP]Malheiros, Denise Maria Avancini CostaReis, Marlene A.Pacheco-Silva, Alvaro [UNIFESP]Câmara, Niels Olsen Saraiva [UNIFESP]2016-01-24T14:17:39Z2016-01-24T14:17:39Z2012-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1727-1741application/pdfhttp://dx.doi.org/10.3727/096368911X623925Cell Transplantation. Putnam Valley: Cognizant Communication Corp, v. 21, n. 8, p. 1727-1741, 2012.10.3727/096368911X623925WOS000311597400011.pdf0963-6897http://repositorio.unifesp.br/handle/11600/34404WOS:000311597400011engCell Transplantationinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-10-10T13:38:35Zoai:repositorio.unifesp.br/:11600/34404Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-10-10T13:38:35Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression
title Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression
spellingShingle Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression
Donizetti-Oliveira, Cassiano [UNIFESP]
Adipose-derived stem cell
Acute kidney injury
Ischemia-reperfusion injury
Fibrosis
Inflammation
title_short Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression
title_full Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression
title_fullStr Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression
title_full_unstemmed Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression
title_sort Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression
author Donizetti-Oliveira, Cassiano [UNIFESP]
author_facet Donizetti-Oliveira, Cassiano [UNIFESP]
Semedo, Patricia [UNIFESP]
Burgos-Silva, Marina [UNIFESP]
Cenedeze, Marco Antonio [UNIFESP]
Malheiros, Denise Maria Avancini Costa
Reis, Marlene A.
Pacheco-Silva, Alvaro [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
author_role author
author2 Semedo, Patricia [UNIFESP]
Burgos-Silva, Marina [UNIFESP]
Cenedeze, Marco Antonio [UNIFESP]
Malheiros, Denise Maria Avancini Costa
Reis, Marlene A.
Pacheco-Silva, Alvaro [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Univ Fed Triangulo Mineiro
dc.contributor.author.fl_str_mv Donizetti-Oliveira, Cassiano [UNIFESP]
Semedo, Patricia [UNIFESP]
Burgos-Silva, Marina [UNIFESP]
Cenedeze, Marco Antonio [UNIFESP]
Malheiros, Denise Maria Avancini Costa
Reis, Marlene A.
Pacheco-Silva, Alvaro [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
dc.subject.por.fl_str_mv Adipose-derived stem cell
Acute kidney injury
Ischemia-reperfusion injury
Fibrosis
Inflammation
topic Adipose-derived stem cell
Acute kidney injury
Ischemia-reperfusion injury
Fibrosis
Inflammation
description Adipose tissue-derived stem cells (ASCs) are an attractive source of stem cells with regenerative properties that are similar to those of bone marrow stem cells. Here, we analyze the role of ASCs in reducing the progression of kidney fibrosis. Progressive renal fibrosis was achieved by unilateral clamping of the renal pedicle in mice for 1 h; after that, the kidney was reperfused immediately. Four hours after the surgery, 2 x 10(5) ASCs were intraperitoneally administered, and mice were followed for 24 h posttreatment and then at some other time interval for the next 6 weeks. Also, animals were treated with 2 x 10(5) ASCs at 6 weeks after reperfusion and sacrificed 4 weeks later to study their effect when interstitial fibrosis is already present. At 24 h after reperfusion, ASC-treated animals showed reduced renal dysfunction and enhanced regenerative tubular processes. Renal mRNA expression of IL-6 and TNF was decreased in ASC-treated animals, whereas IL-4. IL-10, and HO-1 expression increased despite a lack of ASCs in the kidneys as determined by SRY analysis. As expected, untreated kidneys shrank at 6 weeks, whereas the kidneys of ASC-treated animals remained normal in size, showed less collagen deposition, and decreased staining for FSP-1, type I collagen, and Hypoxyprobe. the renal protection seen in ASC-treated animals was followed by reduced serum levels of TNF-alpha, KC, RANTES, and IL-1 alpha. Surprisingly, treatment with ASCs at 6 weeks, when animals already showed installed fibrosis, demonstrated amelioration of functional parameters, with less tissue fibrosis observed and reduced mRNA expression of type I collagen and vimentin. ASC therapy can improve functional parameters and reduce progression of renal fibrosis at early and later times after injury, mostly due to early modulation of the inflammatory response and to less hypoxia, thereby reducing the epithelial-mesenchymal transition.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-01
2016-01-24T14:17:39Z
2016-01-24T14:17:39Z
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/10.3727/096368911X623925
Cell Transplantation. Putnam Valley: Cognizant Communication Corp, v. 21, n. 8, p. 1727-1741, 2012.
10.3727/096368911X623925
WOS000311597400011.pdf
0963-6897
http://repositorio.unifesp.br/handle/11600/34404
WOS:000311597400011
url http://dx.doi.org/10.3727/096368911X623925
http://repositorio.unifesp.br/handle/11600/34404
identifier_str_mv Cell Transplantation. Putnam Valley: Cognizant Communication Corp, v. 21, n. 8, p. 1727-1741, 2012.
10.3727/096368911X623925
WOS000311597400011.pdf
0963-6897
WOS:000311597400011
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Cell Transplantation
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1727-1741
application/pdf
dc.publisher.none.fl_str_mv Cognizant Communication Corp
publisher.none.fl_str_mv Cognizant Communication Corp
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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