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凝集素样氧化型低密度脂蛋白受体-1(LOX-1):缺血性卒中的潜在治疗靶点。

Lectin-Like Oxidized Low-Density Lipoprotein Receptor-1 (LOX-1): A Potential Therapeutic Target in Ischemic Stroke.

作者信息

Hu Yue, Li Yuhao, Luo Yumin, Wang Ningqun, Zheng Yangmin

机构信息

Institute of Cerebrovascular Disease Research and Department of Neurology, Xuanwu Hospital of Capital Medical University, Beijing, China.

Beijing Geriatric Medical Research Center, Beijing, China.

出版信息

Transl Stroke Res. 2024 Nov 22. doi: 10.1007/s12975-024-01307-z.

DOI:10.1007/s12975-024-01307-z
PMID:39576412
Abstract

Stroke, the leading cause of disability and the second leading cause of death worldwide, is characterized by high morbidity and disability. The lectin-like oxidized low-density lipoprotein receptor (LOX-1) is a scavenger receptor that promotes endothelial dysfunction by recognizing and internalizing oxidized low-density lipoproteins (ox-LDL) to induce the formation, development, and instability of atherosclerotic plaques, ultimately leading to vascular thrombosis. Previous clinical and epidemiological studies have indicated that LOX-1 plays a vital role in cerebral ischemic injury following ischemic stroke. Multiple clinical studies have shown that the genetic polymorphisms in LOX-1 are associated with susceptibility to ischemic stroke. Soluble LOX-1 (sLOX-1), a biomarker of ischemic stroke, is associated with the prognosis of ischemic stroke. This article discusses the clinical and experimental findings on LOX-1 in ischemic stroke and the development of new therapeutic strategies targeting LOX-1.

摘要

中风是全球致残的主要原因和第二大死因,其特点是高发病率和高致残率。凝集素样氧化低密度脂蛋白受体(LOX-1)是一种清道夫受体,它通过识别和内化氧化低密度脂蛋白(ox-LDL)来促进内皮功能障碍,从而诱导动脉粥样硬化斑块的形成、发展和不稳定,最终导致血管血栓形成。先前的临床和流行病学研究表明,LOX-1在缺血性中风后的脑缺血损伤中起着至关重要的作用。多项临床研究表明,LOX-1的基因多态性与缺血性中风的易感性有关。可溶性LOX-1(sLOX-1)作为缺血性中风的生物标志物,与缺血性中风的预后相关。本文讨论了缺血性中风中LOX-1的临床和实验研究结果以及针对LOX-1的新治疗策略的进展。

相似文献

1
Lectin-Like Oxidized Low-Density Lipoprotein Receptor-1 (LOX-1): A Potential Therapeutic Target in Ischemic Stroke.凝集素样氧化型低密度脂蛋白受体-1(LOX-1):缺血性卒中的潜在治疗靶点。
Transl Stroke Res. 2024 Nov 22. doi: 10.1007/s12975-024-01307-z.
2
Mutation within the transmembrane domain of oxidized low-density lipoprotein receptor 1 influences oxidized low-density lipoprotein-induced signal transduction.氧化型低密度脂蛋白受体1跨膜结构域内的突变影响氧化型低密度脂蛋白诱导的信号转导。
Innate Immun. 2025 Jan-Dec;31:17534259251350447. doi: 10.1177/17534259251350447. Epub 2025 Jun 16.
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High Levels of Soluble Lectinlike Oxidized Low-Density Lipoprotein Receptor-1 Are Associated With Carotid Plaque Inflammation and Increased Risk of Ischemic Stroke.高水平的可溶性凝集素样氧化型低密度脂蛋白受体-1 与颈动脉斑块炎症和缺血性卒中风险增加相关。
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Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1): a crucial driver of atherosclerotic cardiovascular disease.凝集素样氧化型低密度脂蛋白受体-1(LOX-1):动脉粥样硬化性心血管疾病的关键驱动因素。
Eur Heart J. 2021 May 7;42(18):1797-1807. doi: 10.1093/eurheartj/ehaa770.

本文引用的文献

1
Bioactive Flavonoids in Protecting Against Endothelial Dysfunction and Atherosclerosis.生物活性黄酮类化合物对内皮功能障碍和动脉粥样硬化的保护作用。
Handb Exp Pharmacol. 2025;287:1-31. doi: 10.1007/164_2024_715.
2
LOX-1 and MMP-9 Inhibition Attenuates the Detrimental Effects of Delayed rt-PA Therapy and Improves Outcomes After Acute Ischemic Stroke.LOX-1 和 MMP-9 抑制减轻了延迟 rt-PA 治疗的有害影响,并改善了急性缺血性脑卒中后的结局。
Circ Res. 2024 Apr 12;134(8):954-969. doi: 10.1161/CIRCRESAHA.123.323371. Epub 2024 Mar 19.
3
Role of Lectin-Like Oxidized Low-Density Lipoprotein Receptor-1 in Inflammation and Pathogen-Associated Interactions.
凝集素样氧化型低密度脂蛋白受体-1在炎症及病原体相关相互作用中的作用
J Innate Immun. 2024;16(1):105-132. doi: 10.1159/000535793. Epub 2024 Jan 17.
4
Relationship of Soluble Lectin-Like Low-Density Lipoprotein Receptor-1 (sLOX-1) With Inflammation and Coronary Plaque Progression in Psoriasis.银屑病患者可溶性凝集素样低密度脂蛋白受体-1(sLOX-1)与炎症及冠状动脉斑块进展的关系。
J Am Heart Assoc. 2023 Nov 21;12(22):e031227. doi: 10.1161/JAHA.123.031227. Epub 2023 Nov 20.
5
Autophagy: Regulator of cell death.自噬:细胞死亡的调控者。
Cell Death Dis. 2023 Oct 4;14(10):648. doi: 10.1038/s41419-023-06154-8.
6
LOX-1 variants modulate the severity of cardiovascular disease: state of the art and future directions.LOX-1 变体调节心血管疾病的严重程度:最新进展和未来方向。
Mol Cell Biochem. 2024 Sep;479(9):2245-2254. doi: 10.1007/s11010-023-04859-0. Epub 2023 Oct 3.
7
LOX-1 mediates inflammatory activation of microglial cells through the p38-MAPK/NF-κB pathways under hypoxic-ischemic conditions.LOX-1 通过缺氧缺血条件下的 p38-MAPK/NF-κB 通路介导小胶质细胞的炎症激活。
Cell Commun Signal. 2023 Jun 2;21(1):126. doi: 10.1186/s12964-023-01048-w.
8
Autophagic degradation of LOX-1 is involved in the maintenance of vascular integrity injured by oxLDL and protected by Berberine.自噬降解 LOX-1 参与维持 oxLDL 损伤的血管完整性,并受到小檗碱的保护。
Int J Biol Sci. 2023 Mar 21;19(6):1813-1830. doi: 10.7150/ijbs.80958. eCollection 2023.
9
miR-186-5p Dysregulation in Serum Exosomes from Patients with AMI Aggravates Atherosclerosis via Targeting LOX-1.AMI 患者血清外泌体中 miR-186-5p 失调通过靶向 LOX-1 加重动脉粥样硬化。
Int J Nanomedicine. 2022 Dec 13;17:6301-6316. doi: 10.2147/IJN.S383904. eCollection 2022.
10
Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1): a crucial driver of atherosclerotic cardiovascular disease.凝集素样氧化型低密度脂蛋白受体-1(LOX-1):动脉粥样硬化性心血管疾病的关键驱动因素。
Eur Heart J. 2021 May 7;42(18):1797-1807. doi: 10.1093/eurheartj/ehaa770.