Adipose Tissue-Derived Stem Cell Treatment Prevents Renal Disease Progression
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , |
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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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 |
_version_ |
1814268451098722304 |