Suppr超能文献

内皮细胞受体在组织脂质摄取和代谢中的作用。

Endothelial Cell Receptors in Tissue Lipid Uptake and Metabolism.

机构信息

Division of Nutritional Sciences, Department of Medicine, Washington University School of Medicine, Saint Louis, MO (N.A.A., D.S., T.P.).

Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, New York University Grossman School of Medicine (A.G.C., D.B., I.J.G.).

出版信息

Circ Res. 2021 Feb 5;128(3):433-450. doi: 10.1161/CIRCRESAHA.120.318003. Epub 2021 Feb 4.

Abstract

Lipid uptake and metabolism are central to the function of organs such as heart, skeletal muscle, and adipose tissue. Although most heart energy derives from fatty acids (FAs), excess lipid accumulation can cause cardiomyopathy. Similarly, high delivery of cholesterol can initiate coronary artery atherosclerosis. Hearts and arteries-unlike liver and adrenals-have nonfenestrated capillaries and lipid accumulation in both health and disease requires lipid movement from the circulation across the endothelial barrier. This review summarizes recent in vitro and in vivo findings on the importance of endothelial cell receptors and uptake pathways in regulating FAs and cholesterol uptake in normal physiology and cardiovascular disease. We highlight clinical and experimental data on the roles of ECs in lipid supply to tissues, heart, and arterial wall in particular, and how this affects organ metabolism and function. Models of FA uptake into ECs suggest that receptor-mediated uptake predominates at low FA concentrations, such as during fasting, whereas FA uptake during lipolysis of chylomicrons may involve paracellular movement. Similarly, in the setting of an intact arterial endothelial layer, recent and historic data support a role for receptor-mediated processes in the movement of lipoproteins into the subarterial space. We conclude with thoughts on the need to better understand endothelial lipid transfer for fuller comprehension of the pathophysiology of hyperlipidemia, and lipotoxic diseases such as some forms of cardiomyopathy and atherosclerosis.

摘要

脂质摄取和代谢是心脏、骨骼肌和脂肪组织等器官功能的核心。尽管大多数心脏能量来自脂肪酸 (FA),但过量的脂质积累会导致心肌病。同样,胆固醇的高输送会引发冠状动脉粥样硬化。与肝脏和肾上腺不同,心脏和动脉没有有窗孔的毛细血管,在健康和疾病状态下,脂质的积累都需要从循环系统穿过内皮屏障进入细胞内。本综述总结了最近关于内皮细胞受体和摄取途径在调节正常生理和心血管疾病中 FA 和胆固醇摄取的重要性的体外和体内发现。我们强调了关于内皮细胞在组织、心脏和动脉壁的脂质供应中的作用的临床和实验数据,以及这如何影响器官代谢和功能。FA 摄取进入内皮细胞的模型表明,在低 FA 浓度下,如在禁食期间,受体介导的摄取占主导地位,而在乳糜微粒脂肪分解期间,FA 的摄取可能涉及细胞旁运动。同样,在完整的动脉内皮层的情况下,最近和历史数据支持受体介导的过程在脂蛋白进入亚动脉空间的运动中的作用。我们最后认为,需要更好地理解内皮细胞脂质转移,以更全面地理解高脂血症和脂肪毒性疾病(如某些形式的心肌病和动脉粥样硬化)的病理生理学。

相似文献

1
Endothelial Cell Receptors in Tissue Lipid Uptake and Metabolism.内皮细胞受体在组织脂质摄取和代谢中的作用。
Circ Res. 2021 Feb 5;128(3):433-450. doi: 10.1161/CIRCRESAHA.120.318003. Epub 2021 Feb 4.
2
Endothelial cell CD36 optimizes tissue fatty acid uptake.内皮细胞 CD36 优化组织脂肪酸摄取。
J Clin Invest. 2018 Oct 1;128(10):4329-4342. doi: 10.1172/JCI99315. Epub 2018 Jul 26.

引用本文的文献

8
Nitrosation of CD36 Regulates Endothelial Function and Serum Lipids.CD36的亚硝化作用调节内皮功能和血脂。
Arterioscler Thromb Vasc Biol. 2025 Jul;45(7):1067-1086. doi: 10.1161/ATVBAHA.124.321964. Epub 2025 Apr 17.

本文引用的文献

1
Targeting metabolic pathways to treat cardiovascular diseases.靶向代谢途径治疗心血管疾病。
Biochim Biophys Acta Mol Basis Dis. 2020 Oct 1;1866(10):165879. doi: 10.1016/j.bbadis.2020.165879. Epub 2020 Jun 18.
6
Scavenger receptor class B, type 1 facilitates cellular fatty acid uptake.清道夫受体 B 类,亚型 1 促进细胞脂肪酸摄取。
Biochim Biophys Acta Mol Cell Biol Lipids. 2020 Feb;1865(2):158554. doi: 10.1016/j.bbalip.2019.158554. Epub 2019 Oct 31.
9
Structure of lipoprotein lipase in complex with GPIHBP1.脂蛋白脂肪酶与 GPIHBP1 复合物的结构。
Proc Natl Acad Sci U S A. 2019 May 21;116(21):10360-10365. doi: 10.1073/pnas.1820171116. Epub 2019 May 9.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验