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1.
World J Hepatol ; 15(6): 725-740, 2023 Jun 27.
Artigo em Inglês | MEDLINE | ID: mdl-37397935

RESUMO

Non-alcoholic fatty liver disease (NAFLD) or metabolic (dysfunction)-associated fatty liver disease is the leading cause of chronic liver diseases defined as a disease spectrum comprising hepatic steatosis, non-alcoholic steatohepatitis (NASH), liver fibrosis, cirrhosis, and hepatic carcinoma. NASH, characterized by hepatocyte injury, steatosis, inflammation, and fibrosis, is associated with NAFLD prognosis. Ductular reaction (DR) is a common compensatory reaction associated with liver injury, which involves the hepatic progenitor cells (HPCs), hepatic stellate cells, myofibroblasts, inflammatory cells (such as macrophages), and their secreted substances. Recently, several studies have shown that the extent of DR parallels the stage of NASH and fibrosis. This review summarizes previous research on the correlation between DR and NASH, the potential interplay mechanism driving HPC differentiation, and NASH progression.

2.
J Cell Mol Med ; 24(17): 9774-9785, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32790017

RESUMO

Previous studies revealed that caspase recruitment domain protein 9 (CARD9) was involved in severe acute pancreatitis (SAP) inflammation and that interfering with its expression in vivo could inhibit inflammation. However, the specific mechanism is unknown. This study aimed to discover the related signal pathways of CARD9 in macrophages. SiRNA interference technology was used in vivo and in vitro to detect CARD9-related signal pathways in peritoneal macrophages. Furthermore, Toll-like receptor 4 (TLR4) and membrane-associated C-type lectin-1 (Dectin-1) pathways in macrophages were activated specially to looking for the upstream signal path of CARD9. Results showed up-regulation of CARD9 expression in peritoneal macrophages of SAP rats (P < .05). CARD9 siRNA alleviated inflammatory cytokines, and inhibited the phosphorylation of NF-κB and p38MAPK in peritoneal macrophages in vivo or in vitro. Meanwhile, CARD9 siRNA reduced the concentration of CARD9 and Bcl10 in peritoneal macrophages, and TLR4 and Dectin-1 took part in CARD9 signal pathways in macrophages. In conclusion, there is an inflammation signal pathway comprised of TLR4/Dectin-1-CARD9-NF-κB/p38MAPK activated in macrophages in SAP. Blockade of CARD9 expression in macrophages can effectively alleviate SAP inflammation.


Assuntos
Proteínas Adaptadoras de Sinalização CARD/genética , Inflamação/genética , Lectinas Tipo C/genética , Pancreatite/genética , Receptor 4 Toll-Like/genética , Animais , Proteínas Adaptadoras de Sinalização CARD/antagonistas & inibidores , Modelos Animais de Doenças , Regulação da Expressão Gênica/genética , Humanos , Inflamação/patologia , Macrófagos/metabolismo , Macrófagos/patologia , NF-kappa B/genética , Pancreatite/patologia , Peritônio/metabolismo , Peritônio/patologia , RNA Interferente Pequeno/farmacologia , Ratos , Índice de Gravidade de Doença , Transdução de Sinais/genética , Receptor 4 Toll-Like/antagonistas & inibidores , Proteínas Quinases p38 Ativadas por Mitógeno/genética
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