Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, 28 West Changsheng Road, Hengyang 421001, Hunan, China; Nursing School, University of South China, Hengyang 421001, Hunan, China; Department of Biochemistry and Molecular Biology, The Libin Cardiovascular Institute of Alberta, Cumming School of Medicine, The University of Calgary, Health Sciences Center, 3330 Hospital Dr. NW, Calgary, Alberta T2N 4N1, Canada.
Department of Practice Educational, Office of Academic Affairs, Guilin Medical University, Guilin, Guangxi 541004, China.
Clin Chim Acta. 2018 May;480:126-137. doi: 10.1016/j.cca.2018.02.006. Epub 2018 Feb 14.
Lipoprotein lipase (LPL) is a rate-limiting enzyme that catalyzes hydrolysis of the triglyceride (TG) core of circulating TG-rich lipoproteins including chylomicrons (CM), low-density lipoproteins (LDL) and very low-density lipoproteins (VLDL). A variety of parenchymal cells can synthesize and secrete LPL. Recent studies have demonstrated that complicated processes are involved in LPL biosynthesis, secretion and transport. The enzyme activity of LPL is regulated by many factors, such as apolipoproteins, angiopoietins, hormones and miRNAs. In this article, we also reviewed the roles of LPL in atherosclerosis, coronary heart disease, cerebrovascular accident, Alzheimer disease and chronic lymphocytic leukemia. LPL in different tissues exerts differential physiological functions. The role of LPL in atherosclerosis is still controversial as reported in the literature. Here, we focused on the properties of LPL derived from macrophages, endothelial cells and smooth muscle cells in the vascular wall. We also explore the existence of crosstalk between LPL and those cells when the molecule mainly plays a proatherogenic role. This review will provide insightful knowledge of LPL and open new therapeutic perspectives.
脂蛋白脂肪酶(LPL)是一种限速酶,可催化包括乳糜微粒(CM)、低密度脂蛋白(LDL)和极低密度脂蛋白(VLDL)在内的循环富含甘油三酯(TG)脂蛋白的 TG 核心水解。各种实质细胞都可以合成和分泌 LPL。最近的研究表明,LPL 的生物合成、分泌和转运涉及复杂的过程。LPL 的酶活性受许多因素的调节,如载脂蛋白、血管生成素、激素和 miRNAs。在本文中,我们还综述了 LPL 在动脉粥样硬化、冠心病、脑血管意外、阿尔茨海默病和慢性淋巴细胞白血病中的作用。不同组织中的 LPL 发挥着不同的生理功能。正如文献报道的那样,LPL 在动脉粥样硬化中的作用仍存在争议。在这里,我们主要关注血管壁中巨噬细胞、内皮细胞和平滑肌细胞来源的 LPL 的特性。我们还探讨了当该分子主要发挥促动脉粥样硬化作用时,LPL 与这些细胞之间存在的串扰。这篇综述将为 LPL 提供有见地的知识,并开辟新的治疗视角。