College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Gwanakro 1, Gwanak-gu, Seoul 08826, Republic of Korea.
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Gwanakro 1, Gwanak-gu, Seoul 08826, Republic of Korea.
Biochem Pharmacol. 2019 Aug;166:46-55. doi: 10.1016/j.bcp.2019.05.011. Epub 2019 May 8.
Acetaminophen (APAP)-induced liver injury (AILI) is initiated by the generation of a reactive metabolite and ultimately leads to hepatocyte necrosis. Necrotic cells secrete damage-associated molecular patterns that activate hepatic nonparenchymal cells and induce an inflammatory response. Fetuin-A is a hepatokine with reported involvement in low-grade inflammation in many diseases, due to acting as an endogenous ligand for TLR4. However, little is known about the role of fetuin-A in AILI. In this study, we showed that fetuin-A is involved in the aggravation of hepatotoxicity during the initial phase of AILI progression. Treatment with APAP increased the expression and serum levels of fetuin-A in mice. Fetuin-A upregulated transcription of pro-inflammatory cytokines and chemokines through activation of TLR4 and also increased monocyte infiltration into the liver, leading to necroinflammatory reactions in AILI. However, these reactions were attenuated with the silencing of fetuin-A using adenoviral shRNA. As a result, mice with silenced fetuin-A exhibited less centrilobular necrosis and liver injury compared to controls in response to APAP. In conclusion, our results suggest that fetuin-A is an important hepatokine that mediates the hepatotoxicity of APAP through production of chemokines and thus regulates the infiltration of monocytes into the liver, a critical event in the inflammatory response during the initial phase of AILI. Our results indicate that a strategy based on the antagonism of fetuin-A may be a novel therapeutic approach to the treatment of acetaminophen-induced acute liver failure.
对乙酰氨基酚(APAP)诱导的肝损伤(AILI)是由活性代谢物的产生引发的,最终导致肝细胞坏死。坏死细胞分泌损伤相关分子模式,激活肝非实质细胞并诱导炎症反应。胎球蛋白-A 是一种肝源细胞因子,据报道,由于其作为 TLR4 的内源性配体,在许多疾病中与低度炎症有关。然而,关于胎球蛋白-A 在 AILI 中的作用知之甚少。在这项研究中,我们表明胎球蛋白-A 参与了 AILI 进展初始阶段肝毒性的加重。APAP 治疗增加了小鼠中胎球蛋白-A 的表达和血清水平。胎球蛋白-A 通过激活 TLR4 上调促炎细胞因子和趋化因子的转录,还增加了单核细胞向肝脏的浸润,导致 AILI 中的坏死性炎症反应。然而,使用腺病毒 shRNA 沉默胎球蛋白-A 可减轻这些反应。结果,与对照组相比,沉默胎球蛋白-A 的小鼠在 APAP 反应中表现出较少的中央小叶坏死和肝损伤。总之,我们的结果表明,胎球蛋白-A 是一种重要的肝源细胞因子,通过产生趋化因子介导 APAP 的肝毒性,从而调节单核细胞向肝脏的浸润,这是 AILI 初始阶段炎症反应中的一个关键事件。我们的结果表明,基于胎球蛋白-A 拮抗的策略可能是治疗对乙酰氨基酚诱导的急性肝衰竭的一种新的治疗方法。