Suppr超能文献

血管壁中的血小板与非血栓性疾病。

Platelets at the Vessel Wall in Non-Thrombotic Disease.

机构信息

Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland, OH (A.A., C.L.J., S.J.C.).

Case Western Reserve University School of Medicine, Cleveland, OH (E.M., S.J.C.).

出版信息

Circ Res. 2023 Mar 17;132(6):775-790. doi: 10.1161/CIRCRESAHA.122.321566. Epub 2023 Mar 16.

Abstract

Platelets are small, anucleate entities that bud from megakaryocytes in the bone marrow. Among circulating cells, platelets are the most abundant cell, traditionally involved in regulating the balance between thrombosis (the terminal event of platelet activation) and hemostasis (a protective response to tissue injury). Although platelets lack the precise cellular control offered by nucleate cells, they are in fact very dynamic cells, enriched in preformed RNA that allows them the capability of de novo protein synthesis which alters the platelet phenotype and responses in physiological and pathological events. Antiplatelet medications have significantly reduced the morbidity and mortality for patients afflicted with thrombotic diseases, including stroke and myocardial infarction. However, it has become apparent in the last few years that platelets play a critical role beyond thrombosis and hemostasis. For example, platelet-derived proteins by constitutive and regulated exocytosis can be found in the plasma and may educate distant tissue including blood vessels. First, platelets are enriched in inflammatory and anti-inflammatory molecules that may regulate vascular remodeling. Second, platelet-derived microparticles released into the circulation can be acquired by vascular endothelial cells through the process of endocytosis. Third, platelets are highly enriched in mitochondria that may contribute to the local reactive oxygen species pool and remodel phospholipids in the plasma membrane of blood vessels. Lastly, platelets are enriched in proteins and phosphoproteins which can be secreted independent of stimulation by surface receptor agonists in conditions of disturbed blood flow. This so-called biomechanical platelet activation occurs in regions of pathologically narrowed (atherosclerotic) or dilated (aneurysmal) vessels. Emerging evidence suggests platelets may regulate the process of angiogenesis and blood flow to tumors as well as education of distant organs for the purposes of allograft health following transplantation. This review will illustrate the potential of platelets to remodel blood vessels in various diseases with a focus on the aforementioned mechanisms.

摘要

血小板是从骨髓中的巨核细胞中芽生而来的小型无核实体。在循环细胞中,血小板是最丰富的细胞,传统上参与调节血栓形成(血小板激活的终末事件)和止血(对组织损伤的保护性反应)之间的平衡。虽然血小板缺乏有核细胞提供的精确细胞控制,但实际上它们是非常活跃的细胞,富含预先形成的 RNA,使它们能够从头合成蛋白质,从而改变血小板表型和在生理和病理事件中的反应。抗血小板药物显著降低了患有血栓性疾病(包括中风和心肌梗死)的患者的发病率和死亡率。然而,在过去几年中,人们已经清楚地认识到,血小板在血栓形成和止血之外发挥着关键作用。例如,血小板衍生的蛋白质通过组成型和调节型胞吐作用可以在血浆中找到,并可能对包括血管在内的远处组织进行教育。首先,血小板富含炎症和抗炎分子,这些分子可能调节血管重塑。其次,释放到循环中的血小板衍生的微泡可以通过内吞作用被血管内皮细胞摄取。第三,血小板富含线粒体,可能有助于局部活性氧物质池的形成,并重塑血管内皮细胞的质膜中的磷脂。最后,血小板富含蛋白质和磷酸化蛋白质,这些蛋白质可以在血流紊乱的情况下独立于表面受体激动剂的刺激而分泌。这种所谓的生物力学血小板激活发生在病理性狭窄(动脉粥样硬化)或扩张(动脉瘤)的血管区域。新出现的证据表明,血小板可能调节血管生成和肿瘤血流以及移植后同种异体移植物健康的远处器官的教育过程。本综述将说明血小板在各种疾病中重塑血管的潜力,重点介绍上述机制。

相似文献

1
Platelets at the Vessel Wall in Non-Thrombotic Disease.
Circ Res. 2023 Mar 17;132(6):775-790. doi: 10.1161/CIRCRESAHA.122.321566. Epub 2023 Mar 16.
2
The Black Book of Psychotropic Dosing and Monitoring.
Psychopharmacol Bull. 2024 Jul 8;54(3):8-59.
4
Pathogen-reduced platelets for the prevention of bleeding.
Cochrane Database Syst Rev. 2013 Mar 28(3):CD009072. doi: 10.1002/14651858.CD009072.pub2.
7
Behavioral interventions to reduce risk for sexual transmission of HIV among men who have sex with men.
Cochrane Database Syst Rev. 2008 Jul 16(3):CD001230. doi: 10.1002/14651858.CD001230.pub2.
9
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.
Cochrane Database Syst Rev. 2017 Dec 22;12(12):CD011535. doi: 10.1002/14651858.CD011535.pub2.
10
Uncommon Non-MS Demyelinating Disorders of the Central Nervous System.
Curr Neurol Neurosci Rep. 2025 Jul 1;25(1):45. doi: 10.1007/s11910-025-01432-8.

引用本文的文献

1
Platelets as drivers of immunothrombosis in rheumatic diseases.
Nat Rev Rheumatol. 2025 Jul 7. doi: 10.1038/s41584-025-01276-z.
2
Special Issue "Molecular Research on Platelet Activity in Health and Disease 2024".
Int J Mol Sci. 2025 Apr 19;26(8):3873. doi: 10.3390/ijms26083873.
3
Endothelial protease-activated receptor 4: impotent or important?
Front Cardiovasc Med. 2025 Jan 28;12:1541879. doi: 10.3389/fcvm.2025.1541879. eCollection 2025.
4
Olfactory Receptors and Aortic Aneurysm: Review of Disease Pathways.
J Clin Med. 2024 Dec 19;13(24):7778. doi: 10.3390/jcm13247778.
5
Platelet pals: How blood cells shape the future of the aorta.
Vasc Med. 2025 Feb;30(1):48-49. doi: 10.1177/1358863X241309832. Epub 2025 Jan 1.
7
The Central Role of Interleukin-1 Signalling in the Pathogenesis of Kawasaki Disease Vasculitis: Path to Translation.
Can J Cardiol. 2024 Dec;40(12):2305-2320. doi: 10.1016/j.cjca.2024.07.023. Epub 2024 Jul 30.
8
A Potential Role for MAGI-1 in the Bi-Directional Relationship Between Major Depressive Disorder and Cardiovascular Disease.
Curr Atheroscler Rep. 2024 Sep;26(9):463-483. doi: 10.1007/s11883-024-01223-5. Epub 2024 Jul 3.
9
Understanding megakaryocyte phenotypes and the impact on platelet biogenesis.
Transfusion. 2024 Jul;64(7):1372-1380. doi: 10.1111/trf.17927. Epub 2024 Jun 26.
10
Current Strategies to Guide the Antiplatelet Therapy in Acute Coronary Syndromes.
Int J Mol Sci. 2024 Apr 3;25(7):3981. doi: 10.3390/ijms25073981.

本文引用的文献

1
Megakaryocytes as the Regulator of the Hematopoietic Vascular Niche.
Front Oncol. 2022 Jun 22;12:912060. doi: 10.3389/fonc.2022.912060. eCollection 2022.
2
Beyond Hemostasis: Platelet Innate Immune Interactions and Thromboinflammation.
Int J Mol Sci. 2022 Mar 31;23(7):3868. doi: 10.3390/ijms23073868.
4
Targeting platelet-derived CXCL12 impedes arterial thrombosis.
Blood. 2022 Apr 28;139(17):2691-2705. doi: 10.1182/blood.2020010140.
5
6
Galectin 3 enhances platelet aggregation and thrombosis via Dectin-1 activation: a translational study.
Eur Heart J. 2022 Oct 7;43(37):3556-3574. doi: 10.1093/eurheartj/ehac034.
7
Sex-Dependent Effect of Platelet Nitric Oxide: Production and Platelet Reactivity in Healthy Individuals.
JACC Basic Transl Sci. 2021 Dec 8;7(1):14-25. doi: 10.1016/j.jacbts.2021.10.009. eCollection 2022 Jan.
8
Galectin-9 activates platelet ITAM receptors glycoprotein VI and C-type lectin-like receptor-2.
J Thromb Haemost. 2022 Apr;20(4):936-950. doi: 10.1111/jth.15625. Epub 2022 Jan 6.
9
CLEC-2-dependent platelet subendothelial accumulation by flow disturbance contributes to atherogenesis in mice.
Theranostics. 2021 Oct 3;11(20):9791-9804. doi: 10.7150/thno.64601. eCollection 2021.
10
Role of Microparticles in Cardiovascular Disease: Implications for Endothelial Dysfunction, Thrombosis, and Inflammation.
Hypertension. 2021 Jun;77(6):1825-1844. doi: 10.1161/HYPERTENSIONAHA.121.16975. Epub 2021 May 12.

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