Department of Medicine, Faculty of Medicine, Research Institute of the McGill University Health Centre, McGill University, Montreal, Quebec, Canada.
Metabolism. 2019 Nov;100:153953. doi: 10.1016/j.metabol.2019.153953. Epub 2019 Aug 1.
Cholesterol efflux is the initial step in the reverse cholesterol transport pathway by which excess cholesterol in peripheral cells is exported and subsequently packaged into high-density lipoprotein (HDL) particles. Adiponectin is the most abundantly secreted adipokine that possesses anti-inflammatory and vasculoprotective properties via interaction with transmembrane receptors, AdipoR1 and AdipoR2. Evidence suggests that low levels of adiponectin may be a useful marker for atherosclerotic disease. A proposed anti-atherogenic mechanism of adiponectin involves its ability to promote cholesterol efflux. We performed a systematic review of the role of adiponectin in cholesterol efflux and HDL biogenesis, and of the proteins and receptors believed to be implicated in this process. Nineteen eligible studies (7 clinical, 11 fundamental, 1 clinical + fundamental) were identified through Ovid Medline, Ovid Embase, and Pubmed, that support the notion that adiponectin plays a key role in promoting ABCA1-dependent cholesterol efflux and in modulating HDL biogenesis via activation of the PPAR-γ/LXR-α signalling pathways in macrophages. AdipoR1 and AdipoR2 are suggested to also be implicated in this process, however the data are conflicting/insufficient to establish any firm conclusions. Once the exact mechanisms are unravelled, adiponectin may be critical in defining future treatment strategies directed towards increasing HDL functionality and ultimately reducing atherosclerotic disease.
胆固醇外排是外周细胞内多余胆固醇通过逆胆固醇转运途径被排出并随后被包装到高密度脂蛋白 (HDL) 颗粒中的初始步骤。脂联素是含量最丰富的分泌脂肪因子,通过与跨膜受体 AdipoR1 和 AdipoR2 相互作用具有抗炎和血管保护特性。有证据表明,脂联素水平低可能是动脉粥样硬化疾病的有用标志物。脂联素的一种拟议的抗动脉粥样硬化机制涉及它促进胆固醇外排的能力。我们对脂联素在胆固醇外排和 HDL 生成中的作用,以及被认为参与该过程的蛋白质和受体进行了系统评价。通过 Ovid Medline、Ovid Embase 和 Pubmed 确定了 19 项符合条件的研究(7 项临床研究,11 项基础研究,1 项临床+基础研究),这些研究支持脂联素在通过激活巨噬细胞中的 PPAR-γ/LXR-α 信号通路促进 ABCA1 依赖性胆固醇外排和调节 HDL 生成方面发挥关键作用的观点。AdipoR1 和 AdipoR2 也被认为参与了这一过程,但数据存在冲突/不足,无法得出任何确定的结论。一旦明确了确切的机制,脂联素对于确定未来旨在增加 HDL 功能并最终减少动脉粥样硬化疾病的治疗策略可能至关重要。