Ji Cheng, Kaplowitz Neil
Gastroenterology/Liver Division, Keck School of Medicine and the Research Center for Liver Disease, University of Southern California and the USC-UCLA Research Center for Alcoholic Liver and Pancreatic Disease, Los Angeles, CA 90033, USA.
J Hepatol. 2006 Aug;45(2):321-33. doi: 10.1016/j.jhep.2006.06.004. Epub 2006 Jun 15.
Hepatocytes contain abundant endoplasmic reticulum (ER) which is essential for protein metabolism and stress signaling. Hepatic viral infections, metabolic disorders, mutations of genes encoding ER-resident proteins, and abuse of alcohol or drugs can induce ER stress. Liver cells cope with ER stress by an adaptive protective response termed unfolded protein response (UPR), which includes enhancing protein folding and degradation in the ER and down-regulating overall protein synthesis. When the UPR adaptation to ER stress is insufficient, the ER stress response unleashes pathological consequences including hepatic fat accumulation, inflammation and cell death which can lead to liver disease or worsen underlying causes of liver injury, such as viral or diabetes-obesity-related liver disease.
肝细胞含有丰富的内质网(ER),内质网对于蛋白质代谢和应激信号传导至关重要。肝脏病毒感染、代谢紊乱、编码内质网驻留蛋白的基因突变以及酗酒或滥用药物均可诱导内质网应激。肝细胞通过一种称为未折叠蛋白反应(UPR)的适应性保护反应来应对内质网应激,该反应包括增强内质网中的蛋白质折叠和降解以及下调整体蛋白质合成。当UPR对内质网应激的适应不足时,内质网应激反应会引发包括肝脂肪堆积、炎症和细胞死亡在内的病理后果,这些后果可导致肝病或使肝损伤的潜在病因恶化,如病毒或糖尿病肥胖相关肝病。