Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2009
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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 State of Sao Paulo Foundation for Research Support (FAPESP)[04/08226-9] Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) State of Sao Paulo Foundation for Research Support (FAPESP)[06/0620-5] Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) State of Sao Paulo Foundation for Research Support (FAPESP)[07/07139-3] Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Brazilian Council of Scientific and Technologic Development[573815/2008-9-CNPq] Ministério da Saúde MS/DECIT Ministério da Saúde MS/DECIT |
Identificador |
STEM CELLS, v.27, n.12, p.3063-3073, 2009 1066-5099 http://producao.usp.br/handle/BDPI/28289 10.1002/stem.214 |
Idioma(s) |
eng |
Publicador |
ALPHAMED PRESS |
Relação |
Stem Cells |
Direitos |
restrictedAccess Copyright ALPHAMED PRESS |
Palavras-Chave | #Mesenchymal stem cell #Ischemia-reperfusion injury #Fibrosis #Chronic renal failure #Kidney fibrosis #MARROW-DERIVED CELLS #FACTOR GENE-THERAPY #OBSTRUCTIVE NEPHROPATHY #INTERSTITIAL FIBROSIS #HEME OXYGENASE-1 #HEART-FAILURE #IN-VIVO #INJURY #PROGRESSION #DISEASE #Cell & Tissue Engineering #Biotechnology & Applied Microbiology #Oncology #Cell Biology #Hematology |
Tipo |
article original article publishedVersion |