Biochemistry and Molecular Biology Unit, Dasman Diabetes Institute, Kuwait City, Kuwait.
Departments of Nutrition, Biochemistry and Molecular Medicine, Université de Montréal, and Montreal Diabetes Research Center, Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, QC, Canada.
Prog Lipid Res. 2020 Nov;80:101067. doi: 10.1016/j.plipres.2020.101067. Epub 2020 Oct 2.
Angiopoietin-like protein (ANGPTL) family members, mainly ANGPTL3, ANGPTL4 and ANGPTL8, are physiological inhibitors of lipoprotein lipase (LPL), and play a critical role in lipoprotein and triglyceride metabolism in response to nutritional cues. ANGPTL8 has been described by different names in various studies and has been ascribed various functions at the systemic and cellular levels. Circulating ANGPTL8 originates mainly from the liver and to a smaller extent from adipose tissues. In the blood, ANGPTL8 forms a complex with ANGPTL3 or ANGPTL4 to inhibit LPL in fed or fasted conditions, respectively. Evidence is emerging for additional intracellular and receptor-mediated functions of ANGPTL8, with implications in NFκB mediated inflammation, autophagy, adipogenesis, intra-cellular lipolysis and regulation of circadian clock. Elevated levels of plasma ANGPTL8 are associated with metabolic syndrome, type 2 diabetes, atherosclerosis, hypertension and NAFLD/NASH, even though the precise relationship is not known. Whether ANGPTL8 has direct pathogenic role in these diseases, remains to be explored. In this review, we develop a balanced view on the proposed association of this protein in the regulation of several pathophysiological processes. We also discuss the well-established functions of ANGPTL8 in lipoprotein metabolism in conjunction with the emerging novel extracellular and intracellular roles of ANGPTL8 and the implicated metabolic and signalling pathways. Understanding the diverse functions of ANGPTL8 in various tissues and metabolic states should unveil new opportunities of therapeutic intervention for cardiometabolic disorders.
血管生成素样蛋白(ANGPTL)家族成员,主要包括 ANGPTL3、ANGPTL4 和 ANGPTL8,是脂蛋白脂肪酶(LPL)的生理性抑制剂,在响应营养信号时在脂蛋白和甘油三酯代谢中发挥关键作用。ANGPTL8 在不同的研究中被不同的名称描述,并在系统和细胞水平上具有不同的功能。循环中的 ANGPTL8 主要来源于肝脏,其次来源于脂肪组织。在血液中,ANGPTL8 与 ANGPTL3 或 ANGPTL4 形成复合物,分别在进食或禁食条件下抑制 LPL。越来越多的证据表明 ANGPTL8 具有额外的细胞内和受体介导的功能,这与 NFκB 介导的炎症、自噬、脂肪生成、细胞内脂肪分解和昼夜节律调节有关。血浆 ANGPTL8 水平升高与代谢综合征、2 型糖尿病、动脉粥样硬化、高血压和非酒精性脂肪性肝病/非酒精性脂肪性肝炎(NAFLD/NASH)相关,尽管确切的关系尚不清楚。ANGPTL8 是否在这些疾病中具有直接的致病作用,仍有待探索。在这篇综述中,我们对该蛋白在调节几种病理生理过程中的作用提出了一种平衡的观点。我们还讨论了 ANGPTL8 在脂蛋白代谢中的既定功能,以及 ANGPTL8 新兴的细胞外和细胞内作用以及涉及的代谢和信号通路。了解 ANGPTL8 在各种组织和代谢状态下的多样化功能,应该为治疗代谢性心血管疾病提供新的机会。