Nanji A A, Lau G K, Tipoe G L, Yuen S T, Chen Y X, Thomas P, Lan H Y
Department of Pathology and Center for the Study of Liver Diseases, The University of Hong Kong and Queen Mary Hospital, Hong Kong.
J Interferon Cytokine Res. 2001 Dec;21(12):1055-62. doi: 10.1089/107999001317205187.
Macrophage migration inhibitory factory (MIF) regulates macrophage accumulation at sites of injury and can promote the inflammatory response. We studied MIF expression in the intragastric feeding rat model for alcoholic liver injury. Male and age-matched female rats were fed ethanol or dextrose with fish oil. Two groups of male rats were fed medium-chain triglycerides with ethanol or dextrose. Analysis of liver histopathology, lipid peroxidation, endotoxin, mRNA, and immunohistochemistry for MIF, tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma) were carried out. Male and female rats fed fish oil and ethanol showed necroinflammatory liver injury and had the highest expression of MIF, TNF-alpha, and IFN-gamma in the liver. Decreased levels of MIF protein were seen in rats with higher endotoxin levels, suggesting that preformed MIF is released into the circulation. MIF is an important mediator of the inflammatory response in alcoholic liver disease and a potential therapeutic target.
巨噬细胞移动抑制因子(MIF)可调节损伤部位巨噬细胞的聚集,并能促进炎症反应。我们在酒精性肝损伤的灌胃大鼠模型中研究了MIF的表达。将雄性大鼠和年龄匹配的雌性大鼠用乙醇或葡萄糖加鱼油喂养。两组雄性大鼠用中链甘油三酯加乙醇或葡萄糖喂养。对肝脏组织病理学、脂质过氧化、内毒素、mRNA进行分析,并对MIF、肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)进行免疫组化分析。用鱼油和乙醇喂养的雄性和雌性大鼠出现坏死性炎症性肝损伤,且肝脏中MIF、TNF-α和IFN-γ的表达最高。内毒素水平较高的大鼠中MIF蛋白水平降低,提示预先形成的MIF被释放到循环中。MIF是酒精性肝病炎症反应的重要介质和潜在的治疗靶点。