Chung Sangwon, Hwang Jin-Taek, Park Jae Ho, Choi Hyo-Kyoung
Korea Food Research Institute, 245, Nongsaengmyeong-ro, Iseo-myeon, Wanju-gun, Jeonbuk 55365, Republic of Korea.
Department of Food Biotechnology, Korea University of Science & Technology, Daejeon 34113, Republic of Korea.
Nutr Res Pract. 2019 Jun;13(3):196-204. doi: 10.4162/nrp.2019.13.3.196. Epub 2019 Apr 12.
BACKGROUND/OBJECTIVES: Non-alcoholic fatty liver disease (NAFLD) is a common metabolic disease triggered by epigenetic alterations, including lysine acetylation at histone or non-histone proteins, affecting the stability or transcription of lipogenic genes. Although various natural dietary compounds have anti-lipogenic effects, their effects on the acetylation status and lipid metabolism in the liver have not been thoroughly investigated.
MATERIALS/METHODS: Following oleic-palmitic acid (OPA)-induced lipid accumulation in HepG2 cells, the acetylation status of histone and non-histone proteins, HAT activity, and mRNA expression of representative lipogenic genes, including γ, , , and , were evaluated. Furthermore, correlations between lipid accumulation and HAT activity for 22 representative natural food extracts (NExs) were evaluated.
Non-histone protein acetylation increased following OPA treatment and the acetylation of histones H3K9, H4K8, and H4K16 was accelerated, accompanied by an increase in HAT activity. OPA-induced increases in the mRNA expression of lipogenic genes were down-regulated by C-646, a p300/CBP-specific inhibitor. Finally, we detected a positive correlation between HAT activity and lipid accumulation (Pearson's correlation coefficient = 0.604) using 22 NExs.
Our results suggest that NExs have novel applications as nutraceutical agents with HAT inhibitor activity for the prevention and treatment of NAFLD.
背景/目的:非酒精性脂肪性肝病(NAFLD)是一种常见的代谢性疾病,由表观遗传改变引发,包括组蛋白或非组蛋白赖氨酸乙酰化,影响脂肪生成基因的稳定性或转录。尽管各种天然膳食化合物具有抗脂肪生成作用,但其对肝脏乙酰化状态和脂质代谢的影响尚未得到充分研究。
材料/方法:在油酸 - 棕榈酸(OPA)诱导HepG2细胞脂质积累后,评估组蛋白和非组蛋白的乙酰化状态、组蛋白乙酰转移酶(HAT)活性以及包括γ、、、和在内的代表性脂肪生成基因的mRNA表达。此外,评估了22种代表性天然食物提取物(NExs)的脂质积累与HAT活性之间的相关性。
OPA处理后非组蛋白乙酰化增加,组蛋白H3K9、H4K8和H4K16的乙酰化加速,同时HAT活性增加。p300/CBP特异性抑制剂C - 646下调了OPA诱导的脂肪生成基因mRNA表达增加。最后,使用22种NExs检测到HAT活性与脂质积累之间存在正相关(皮尔逊相关系数 = 0.604)。
我们的结果表明,NExs作为具有HAT抑制剂活性的营养保健品在预防和治疗NAFLD方面具有新的应用。