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The role of hepatic macrophages in nonalcoholic fatty liver disease and nonalcoholic steatohepatitis

机译:肝巨噬细胞在非酒精性脂肪肝和非酒精性脂肪性肝炎中的作用

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摘要

Nonalcoholic steatohepatitis (NASH) is becoming common chronic liver disease because of the increasing global prevalence of obesity and consequently Nonalcoholic fatty liver disease (NAFLD). However, the mechanism for progression of NAFLD to NASH and then cirrhosis is not completely understood, yet. The triggering of these hepatic diseases is thought from hepatocyte injury caused by over-accumulated lipid toxicity. Injured hepatocytes release damage-associated molecular patterns (DAMPs), which can stimulate the Kupffer cells (KCs), liver-resident macrophages, to release pro-inflammatory cytokines and chemokines, and recruit monocyte-derived macrophages (MDMs). The increased activation of KCs and recruitment of MDMs accelerate the progression of NAFLD to NASH and cirrhosis. Therefore, characterization for activation of hepatic macrophages, both KCs and MDMs, is a baseline to figure out the progression of hepatic diseases. The purpose of this review is to discuss the current understanding of mechanisms of NAFLD and NASH, mainly focusing on characterization and function of hepatic macrophages and suggests the regulators of hepatic macrophages as the therapeutic target in hepatic diseases.
机译:非酒精性脂肪性肝炎(NASH)由于肥胖症的全球患病率上升,因此正成为非酒精性脂肪性肝病(NAFLD)的常见慢性肝病。然而,NAFLD发展为NASH然后肝硬化的机制尚不完全清楚。这些肝病的触发是由于脂质毒性过度积累引起的肝细胞损伤。受伤的肝细胞释放损伤相关分子模式(DAMP),可刺激库普弗细胞(KCs),肝驻留巨噬细胞释放促炎性细胞因子和趋化因子,并募集单核细胞衍生的巨噬细胞(MDM)。 KCs的激活增加和MDM的募集加速了NAFLD向NASH和肝硬化的发展。因此,表征肝巨噬细胞(KCs和MDMs)的活化是确定肝病进展的基线。这篇综述的目的是讨论目前对NAFLD和NASH机制的理解,主要侧重于肝巨噬细胞的表征和功能,并提出将肝巨噬细胞作为肝病治疗靶点的调节剂。

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