Decreased protein activator of interferon induced protein kinase (PRKRA) involved in menopause-related cholesterol metabolic disorders by regulating cholesterol biosynthesis.

IF 3.9 2区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Le Xu, Jian Xu, Wanting Shi, Sa Zhang, Ting Guo, Shien Zou
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引用次数: 0

Abstract

Background: Menopause-related cholesterol metabolic disorders pose a global health concern, but the underlying mechanism is unclear. PRKRA was identified as a potential regulator of cholesterol metabolism in an exome-wide association study. Our prior research revealed a decrease in PRKRA expression in the ovarian cortex of postmenopausal women. However, its involvement in cholesterol metabolism disturbances in postmenopausal females remains unclear. This study aimed to investigate the association between PRKRA and cholesterol metabolism disorders in ovariectomized mice. Additionally, we elucidated the impact and underlying mechanisms of PRKRA on cholesterol metabolism in HepG2 and HuH7 cells.

Methods: An ovariectomized mouse model was generated, and the mice were fed a standard diet for six months to simulate menopausal conditions. PRKRA expression in mouse liver tissue was evaluated by qPCR and western blotting. Spearman correlation analysis was used to explore the relationship between the PRKRA mRNA level and the serum total cholesterol concentration. In vitro, we investigated the influence of PRKRA on cholesterol levels and Dil-LDL uptake capacity in HepG2 and HuH7 cells. Additionally, transcriptome sequencing was employed to analyze the intrinsic mechanisms involved.

Results: The ovariectomized mouse model exhibited abnormal lipid profiles that correlated with reduced PRKRA expression in the liver. In vitro, 17β-estradiol (E2) upregulated PRKRA expression, while follicle-stimulating hormone (FSH) downregulated it in HepG2 and HuH7 cells. PRKRA knockdown increased intracellular total cholesterol and decreased Dil-LDL uptake, while PRKRA overexpression had the opposite effects. Mechanistically, reduced PRKRA levels were associated with HMGCS1 upregulation and LDLR downregulation.

Conclusion: Ovariectomy for six months independently induced an aberrant cholesterol phenotype in mice. Downregulation of PRKRA was implicated in cholesterol metabolism disturbances related to menopause, potentially through the regulation of cholesterol synthesis and LDL uptake.

干扰素诱导蛋白激酶(PRKRA)蛋白激活因子的降低通过调节胆固醇生物合成参与绝经相关胆固醇代谢紊乱。
背景:绝经相关胆固醇代谢紊乱已引起全球健康关注,但其潜在机制尚不清楚。在一项全外显子组关联研究中,PRKRA被确定为胆固醇代谢的潜在调节因子。我们之前的研究显示绝经后妇女卵巢皮质PRKRA表达减少。然而,其与绝经后女性胆固醇代谢紊乱的关系尚不清楚。本研究旨在探讨PRKRA与去卵巢小鼠胆固醇代谢紊乱之间的关系。此外,我们阐明了PRKRA对HepG2和HuH7细胞胆固醇代谢的影响及其潜在机制。方法:建立小鼠去卵巢模型,给予标准饮食6个月模拟绝经期。采用qPCR和western blotting检测小鼠肝组织中PRKRA的表达。采用Spearman相关分析探讨PRKRA mRNA水平与血清总胆固醇浓度的关系。在体外,我们研究了PRKRA对HepG2和HuH7细胞胆固醇水平和Dil-LDL摄取能力的影响。此外,转录组测序被用于分析所涉及的内在机制。结果:去卵巢小鼠模型表现出与肝脏中PRKRA表达降低相关的异常脂质谱。在体外,17β-雌二醇(E2)上调HepG2和HuH7细胞中PRKRA的表达,而促卵泡激素(FSH)下调其表达。PRKRA敲低会增加细胞内总胆固醇,降低Dil-LDL的摄取,而PRKRA过表达则有相反的效果。从机制上讲,PRKRA水平降低与HMGCS1上调和LDLR下调有关。结论:卵巢切除6个月独立诱导小鼠胆固醇表型异常。PRKRA的下调与更年期相关的胆固醇代谢紊乱有关,可能通过调节胆固醇合成和LDL摄取。
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来源期刊
Lipids in Health and Disease
Lipids in Health and Disease 生物-生化与分子生物学
CiteScore
7.70
自引率
2.20%
发文量
122
审稿时长
3-8 weeks
期刊介绍: Lipids in Health and Disease is an open access, peer-reviewed, journal that publishes articles on all aspects of lipids: their biochemistry, pharmacology, toxicology, role in health and disease, and the synthesis of new lipid compounds. Lipids in Health and Disease is aimed at all scientists, health professionals and physicians interested in the area of lipids. Lipids are defined here in their broadest sense, to include: cholesterol, essential fatty acids, saturated fatty acids, phospholipids, inositol lipids, second messenger lipids, enzymes and synthetic machinery that is involved in the metabolism of various lipids in the cells and tissues, and also various aspects of lipid transport, etc. In addition, the journal also publishes research that investigates and defines the role of lipids in various physiological processes, pathology and disease. In particular, the journal aims to bridge the gap between the bench and the clinic by publishing articles that are particularly relevant to human diseases and the role of lipids in the management of various diseases.
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