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Please use this identifier to cite or link to this item: http://repositorio.ufba.br/ri/handle/ri/16360

Title: Reduction of galectin-3 expression and liver fibrosis after cell therapy in a mouse model of cirrhosis
Other Titles: Cytotherapy
Authors: Oliveira, Sheilla Andrade de
Souza, Bruno Solano de Freitas
Barreto, Elton Pereira Sá
Kaneto, Carla Martins
Almeida Neto, Hélio
Azevedo, Carine Machado
Guimarães, Elisalva Teixeira
Freitas, Luiz Antonio Rodrigues de
Santos, Ricardo Ribeiro dos
Soares, Milena Botelho Pereira
Keywords: carbon tetrachloride;galectin-3;hepatic cirrhosis;mice;stem cells
Issue Date: 2012
Abstract: Background aims Cirrhosis, end-stage liver disease, is caused by different mechanisms of injury, associated with persistent inflammation. Galectin-3 is an important regulator of fibrosis that links chronic inflammation to fibrogenesis. We investigated the role of bone marrow cell (BMC) transplantation in chronic inflammation and hepatic fibrosis. Methods Liver cirrhosis was induced by administration of carbon tetrachloride and ethanol to wild-type C57BL/6 or bone marrow chimeric mice. Bone marrow chimeras were generated by lethal irradiation and transplantation with BMC obtained from green fluorescent protein (GFP+ )donors. Wild-type cirrhotic mice were transplanted with BMC without irradiation. Livers from chimeras and cirrhotic transplanted mice were obtained for evaluation of inflammation, fibrosis and regulatory factors [galectin-3, matrix metallopeptidase (MMP)-9, tissue inhibitor of metalloproteinase (TIMP)-1 and transforming growth factor (TGF)-β]. Results The development of cirrhosis was associated with increased expression of galectin-3 by F4/80+ cells and intense migration of BMC to the liver. Furthermore, when transplanted after the establishment of cirrhosis, BMC also migrated to the liver and localized within the fibrous septa. Two months after BMC therapy, cirrhotic mice had a significant reduction in liver fibrosis and expression of type I collagen. We did not find any difference in levels of TGF-β, TIMP-1 and MMP-9 between saline and BMC groups. However, the numbers of inflammatory cells, phagocytes and galectin-3+ cells were markedly lower in the livers of cirrhotic mice treated with BMC. Conclusions Our results demonstrate an important role for BMC in the regulation of liver fibrosis and that transplantation of BMC can accelerate fibrosis regression through modulatory mechanisms.
Description: Texto completo: acesso restrito. p. 339–349
URI: http://repositorio.ufba.br/ri/handle/ri/16360
ISSN: 1465-3249
Appears in Collections:Artigos Publicados em Periódicos (Medicina)

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