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Relationship between NLRP1 and Liver Dysfunction Following Allogeneic Hematopoietic Stem Cell Transplantation / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 875-879, 2018.
Artigo em Chinês | WPRIM | ID: wpr-689560
ABSTRACT
<p><b>OBJECTIVE</b>To explore the effect of NLRP1 on the liver dysfunction following allogeneic hematopoietic stem cell transplantation(allo-HSCT).</p><p><b>METHODS</b>The mouse model of allo-HSCT was established by using C57BL/6 and NLRP mice were used as the recipients BABL/c mice were used as donors). The chimera rates of donor's bone marrow cells were assayed by flow cytometry. ALT and AST levels were measured by automatic biochemical analyzer. Western blot was used to detect the expressions of NLRP1, the precursor of Caspase-1 and its active segment p20,IL-1β,IL-18 and MPO in livers.</p><p><b>RESULTS</b>The chimera rate was over 96% on the day 14 after allo-HSCT, and showed that the hematopoietic stem cells of donors had been transplanted into recipients. ALT and AST levels were increased from (173.9±12.39)U/L and (283.7±28.00)U/L on day 7 to (3902±1745)U/L and (5316±924)U/L on the day 14 and decreased to (3153±564.4) U/L and (4350±957.7) U/L on the day 28, respectively. Western blot showed that the expression of NLRP1 was increased after allo-HSCT, which displayed a similar trend with the changes of ALT and AST. When knocking out NLRP1, the contents of ALT and AST in the knocked group were significantly decreased in comparison with the group without knocking out. And the expression levels of NLRP1 related inflammatory proteins, precursor of Caspase-1,p20,Mature-IL-1β,Mature-IL-18 and MPO were lower than those in groups without knocking out NLRP1 gene.</p><p><b>CONCLUSION</b>Allo-HSCT can cause the damage of liver function and increase the expression of NLRP1, while knocking out NLRP1 can reduce the damage of liver function, so NLRP1 may be one of the important factors leading to liver dysfunction.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Transplante Homólogo / Transplante de Células-Tronco Hematopoéticas / Proteínas Adaptadoras de Transdução de Sinal / Proteínas Reguladoras de Apoptose / Interleucina-1beta / Hepatopatias / Camundongos Endogâmicos C57BL Tipo de estudo: Estudo prognóstico Limite: Animais Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2018 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Transplante Homólogo / Transplante de Células-Tronco Hematopoéticas / Proteínas Adaptadoras de Transdução de Sinal / Proteínas Reguladoras de Apoptose / Interleucina-1beta / Hepatopatias / Camundongos Endogâmicos C57BL Tipo de estudo: Estudo prognóstico Limite: Animais Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2018 Tipo de documento: Artigo