Suppr超能文献

microRNA-378b 通过靶向 CaMKK2 调节脂质代谢来调控乙醇诱导的肝脂肪变性。

microRNA-378b regulates ethanol-induced hepatic steatosis by targeting CaMKK2 to mediate lipid metabolism.

机构信息

College of Pharmacy, Guilin Medical University, Guilin, China.

Center for Diabetic Systems Medicine, Guangxi Key Laboratory of Excellence, Guilin, China.

出版信息

Bioengineered. 2021 Dec;12(2):12659-12676. doi: 10.1080/21655979.2021.2003677.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fc/8810039/9065849db7a3/KBIE_A_2003677_F0001_OC.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验