Jeon Joong-Won, Lee Seung Hwan, Kim Donghyun, Sung Jong Hwan
Department of Chemical Engineering, Hongik University, Seoul, Republic of Korea.
Department of Bionano Engineering, Hanyang University, Ansan, Republic of Korea.
Biotechnol Prog. 2021 May;37(3):e3121. doi: 10.1002/btpr.3121. Epub 2021 Jan 15.
Hepatic steatosis, also known as fatty liver disease, occurs due to abnormal lipid accumulation in the liver. It has been known that gut absorption also plays an important role in the mechanism underlying hepatic steatosis. Conventional in vitro cell culture models have limitations in recapitulating the mechanisms of hepatic steatosis because it does not include the gut absorption process. Previously, we reported development of a microfluidic gut-liver chip that can recapitulate the gut absorption of fatty acids and subsequent lipid accumulation in liver cells. In this study, we performed a series of experiments to verify that our gut-liver chip reproduces various aspects of hepatic steatosis. The absorption of fatty acids was evaluated under various culture conditions. The anti-steatotic effect of turofexorate isopropyl (XL-335) and metformin was tested, and both drugs showed different action mechanisms. In addition, the oxidative stress induced by lipid absorption was evaluated. Our results demonstrate the potential of the gut-liver chip for use as a novel, physiologically realistic in vitro model to study fatty liver disease.
肝脂肪变性,也称为脂肪肝疾病,是由于肝脏中脂质异常蓄积所致。众所周知,肠道吸收在肝脂肪变性的潜在机制中也起着重要作用。传统的体外细胞培养模型在概括肝脂肪变性机制方面存在局限性,因为它不包括肠道吸收过程。此前,我们报道了一种微流控肠-肝芯片的开发,该芯片能够概括脂肪酸的肠道吸收以及随后肝细胞中的脂质蓄积。在本研究中,我们进行了一系列实验,以验证我们的肠-肝芯片能够再现肝脂肪变性的各个方面。在各种培养条件下评估脂肪酸的吸收。测试了异异丙基图罗非索酯(XL-335)和二甲双胍的抗脂肪变性作用,两种药物显示出不同的作用机制。此外,还评估了脂质吸收诱导的氧化应激。我们的结果证明了肠-肝芯片作为一种新型的、生理上逼真的体外模型用于研究脂肪肝疾病的潜力。