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J Gastroenterol Hepatol ; 22(11): 2001-8, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17914983

RESUMO

BACKGROUND AND AIM: Bone marrow derived cells are involved in the process of hepatic fibrosis secondary to chronic injury. However, it is not yet known how quickly this event occurs in acute fibrosis models. The purpose of this study was to determine the role of bone marrow cells in rapid fibrosis following bile duct ligation in mice using green fluorescent protein (GFP) expressing bone marrow cells. METHOD: After whole body irradiation, 1 x 10(6) donor whole bone marrow cells from green fluorescent protein(+/-) mice were transplanted into C57BL/6 recipients via the tail vein. Four weeks after bone marrow transplantation, chimeric mice were subjected to common bile duct ligation, and livers of these animals were histologically examined after bile duct ligation using anti-fibroblast specific protein (FSP)-1 antibody and anti-alpha-smooth muscle actin (alpha-SMA) antibody. RESULTS: Periductal fibrosis consisting of fibroblast specific protein-positive cells was demonstrated histologically as early as day 7. Most of the fibrotic cells were green fluorescent protein-negative, however, a significant number of cells were green fluorescent protein-positive and some were also anti-FSP or alpha-SMA-positive. CONCLUSION: Differentiation of bone marrow derived cells into activated fibroblast and myofibroblast-like phenotypes occurs in the very early course of periductal fibrosis following bile duct ligation, suggesting a new strategy for prevention of biliary fibrosis by inhibiting migration of bone marrow cells to liver.


Assuntos
Células da Medula Óssea/metabolismo , Transplante de Medula Óssea , Doenças do Ducto Colédoco/complicações , Ducto Colédoco/cirurgia , Cirrose Hepática/patologia , Actinas/metabolismo , Animais , Proteínas de Ligação ao Cálcio/metabolismo , Diferenciação Celular , Movimento Celular , Quimera , Doenças do Ducto Colédoco/metabolismo , Doenças do Ducto Colédoco/patologia , Doenças do Ducto Colédoco/fisiopatologia , Modelos Animais de Doenças , Fibroblastos/metabolismo , Proteínas de Fluorescência Verde/genética , Proteínas de Fluorescência Verde/metabolismo , Ligadura , Cirrose Hepática/etiologia , Cirrose Hepática/metabolismo , Cirrose Hepática/fisiopatologia , Testes de Função Hepática , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Transgênicos , Proteína A4 de Ligação a Cálcio da Família S100 , Proteínas S100 , Fatores de Tempo , Irradiação Corporal Total
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