College of Pharmacy, Guilin Medical University, Guilin, China.
Center for Diabetic Systems Medicine, Guangxi Key Laboratory of Excellence, Guilin, China.
Bioengineered. 2021 Dec;12(2):12659-12676. doi: 10.1080/21655979.2021.2003677.
Alcoholic liver disease (ALD) has seriously harmed the health of people worldwide, but its underlying mechanisms remain unclear. This study aims to clarify the biological function of microRNA-378b (miR-378b) in ethanol (EtOH)-induced hepatic lipid accumulation. Here, we report miR-378b is over-expressed in EtOH-induced cells and EtOH-fed mice and finally accelerates lipid accumulation. MiR-378b directly targets Ca/calmodulin-dependent protein kinase kinase 2 (CaMKK2), a kinase of AMP-activated protein kinase (AMPK), and mediates the protein level of CaMKK2. Over-expression of miR-378b exacerbated the lipid accumulation induced by EtOH and inhibited CaMKK2 and the AMPK cascade while inhibition of miR-378b ameliorated lipid metabolism dysfunction in vivo and in vitro. In brief, our results show that miR-378b plays an important role in the regulation of lipid metabolism by directly targeting CaMKK2.
酒精性肝病(ALD)严重危害着全世界人民的健康,但其潜在机制仍不清楚。本研究旨在阐明 microRNA-378b(miR-378b)在乙醇(EtOH)诱导的肝脂质积累中的生物学功能。在这里,我们报告 miR-378b 在 EtOH 诱导的细胞和 EtOH 喂养的小鼠中过度表达,并最终加速脂质积累。miR-378b 直接靶向 Ca/钙调蛋白依赖性蛋白激酶激酶 2(CaMKK2),一种 AMP 激活蛋白激酶(AMPK)的激酶,并介导 CaMKK2 的蛋白水平。miR-378b 的过表达加剧了 EtOH 诱导的脂质积累,并抑制了 CaMKK2 和 AMPK 级联,而抑制 miR-378b 则改善了体内和体外的脂质代谢功能障碍。总之,我们的研究结果表明,miR-378b 通过直接靶向 CaMKK2 ,在脂质代谢的调控中发挥重要作用。