Guo Xiaoli, Zhou Qianqian, Jin Jiaming, Lan Fangren, Wen Chaoliang, Li Junying, Yang Ning, Sun Congjiao
National Engineering Laboratory for Animal Breeding and Key Laboratory of Animal Genetics, Breeding and Reproduction, Ministry of Agriculture and Rural Affairs, China Agricultural University, Beijing, 100193, China.
J Anim Sci Biotechnol. 2023 Aug 12;14(1):108. doi: 10.1186/s40104-023-00910-8.
Hepatic steatosis is a prevalent manifestation of fatty liver, that has detrimental effect on the health and productivity of laying hens, resulting in economic losses to the poultry industry. Here, we aimed to systematically investigate the genetic regulatory mechanisms of hepatic steatosis in laying hens.
Ninety individuals with the most prominent characteristics were selected from 686 laying hens according to the accumulation of lipid droplets in the liver, and were graded into three groups, including the control, mild hepatic steatosis and severe hepatic steatosis groups. A combination of transcriptome, proteome, acetylome and lipidome analyses, along with bioinformatics analysis were used to screen the key biological processes, modifications and lipids associated with hepatic steatosis.
The rationality of the hepatic steatosis grouping was verified through liver biochemical assays and RNA-seq. Hepatic steatosis was characterized by increased lipid deposition and multiple metabolic abnormalities. Integration of proteome and acetylome revealed that differentially expressed proteins (DEPs) interacted with differentially acetylated proteins (DAPs) and were involved in maintaining the metabolic balance in the liver. Acetylation alterations mainly occurred in the progression from mild to severe hepatic steatosis, i.e., the enzymes in the fatty acid oxidation and bile acid synthesis pathways were significantly less acetylated in severe hepatic steatosis group than that in mild group (P < 0.05). Lipidomics detected a variety of sphingolipids (SPs) and glycerophospholipids (GPs) were negatively correlated with hepatic steatosis (r ≤ -0.5, P < 0.05). Furthermore, the severity of hepatic steatosis was associated with a decrease in cholesterol and bile acid synthesis and an increase in exogenous cholesterol transport.
In addition to acquiring a global and thorough picture of hepatic steatosis in laying hens, we were able to reveal the role of acetylation in hepatic steatosis and depict the changes in hepatic cholesterol metabolism. The findings provides a wealth of information to facilitate a deeper understanding of the pathophysiology of fatty liver and contributes to the development of therapeutic strategies.
肝脂肪变性是脂肪肝的一种常见表现,对蛋鸡的健康和生产性能具有不利影响,给家禽业带来经济损失。在此,我们旨在系统研究蛋鸡肝脂肪变性的遗传调控机制。
根据肝脏中脂滴的积累情况,从686只蛋鸡中挑选出90只具有最显著特征的个体,并分为三组,包括对照组、轻度肝脂肪变性组和重度肝脂肪变性组。采用转录组、蛋白质组、乙酰化组和脂质组分析相结合的方法,并结合生物信息学分析,筛选与肝脂肪变性相关的关键生物学过程、修饰和脂质。
通过肝脏生化检测和RNA测序验证了肝脂肪变性分组的合理性。肝脂肪变性的特征是脂质沉积增加和多种代谢异常。蛋白质组和乙酰化组的整合显示,差异表达蛋白(DEPs)与差异乙酰化蛋白(DAPs)相互作用,并参与维持肝脏的代谢平衡。乙酰化改变主要发生在从轻度到重度肝脂肪变性的进展过程中,即重度肝脂肪变性组中脂肪酸氧化和胆汁酸合成途径中的酶乙酰化程度明显低于轻度组(P < 0.05)。脂质组学检测到多种鞘脂(SPs)和甘油磷脂(GPs)与肝脂肪变性呈负相关(r ≤ -0.5,P < 0.05)。此外,肝脂肪变性的严重程度与胆固醇和胆汁酸合成减少以及外源性胆固醇转运增加有关。
除了全面深入了解蛋鸡肝脂肪变性外,我们还能够揭示乙酰化在肝脂肪变性中的作用,并描绘肝脏胆固醇代谢的变化。这些发现提供了丰富的信息,有助于更深入地理解脂肪肝的病理生理学,并为治疗策略的开发做出贡献。