Suppr超能文献

血小板促进内皮细胞在基质胶上形成管腔的证据。

Evidence that platelets promote tube formation by endothelial cells on matrigel.

作者信息

Pipili-Synetos E, Papadimitriou E, Maragoudakis M E

机构信息

Department of Pharmacology, Medical School, University of Patras, Greece.

出版信息

Br J Pharmacol. 1998 Nov;125(6):1252-7. doi: 10.1038/sj.bjp.0702191.

Abstract

The involvement of platelets in neovascularization was investigated in the matrigel tube formation assay, an in vitro model of angiogenesis. Platelets promoted the formation of capillary-like structures (expressed as relative tube area) number- and time-dependently. Relative tube area increased from 0.98+/-0.02 (n = 8) in the presence of 6.25 x 10(4), to 3.21+/-0.12 (n=8) in the presence of 10(6) platelets/well compared to 0.54+/-0.04 (n=8) in their absence. This increase was unaffected by acetyl salicylic acid (ASA), apyrase, and hirudin. Photographs from representative experiments, showed that platelets adhered along the differentiating endothelium. Addition of alpha-thrombin (0.1-1 i.u. ml(-1)), the nitric oxide (NO) donor sodium nitroprusside (SNP; 1-100 microM) or the NO synthase inhibitor, L-NG-arginine-methylester (L-NAME, 30-300 microM) to the assay, had no effect on tube formation compared to that seen with platelets alone. Neuraminidase (0.01 i.u./10(7) platelets), which strips sialic acid residues from membrane glycoproteins, abolished the promoting effect of platelets on tube formation. The relative tube area in the presence of neuraminidase-treated platelets was 0.81+/-0.03 (n = 8), in the presence of untreated platelets 1.69+/-0.09, P<0.001 (n=8) and in the absence of platelets, 0.80+/-0.04 (n=8). The tetrapeptide Arg-Gly-Asp-Ser (RGDS; 20-200 microM) which inhibits von Willebrand factor, fibrinogen and fibronectin-mediated adhesion, had no effect on the promoting effect of platelets on tube formation. These results indicate that platelets promote angiogenesis in vitro. This effect is largely independent from activation by alpha-thrombin, is not modified by manipulating NO and prostaglandin metabolism and proceeds possibly through adhesion of the platelets to the differentiating endothelium.

摘要

在基质胶管形成试验(一种血管生成的体外模型)中研究了血小板在新生血管形成中的作用。血小板以数量和时间依赖性方式促进毛细血管样结构的形成(以相对管面积表示)。与不存在血小板时的0.54±0.04(n = 8)相比,在每孔存在6.25×10⁴个血小板时,相对管面积从0.98±0.02(n = 8)增加到每孔存在10⁶个血小板时的3.21±0.12(n = 8)。这种增加不受乙酰水杨酸(ASA)、腺苷三磷酸双磷酸酶和水蛭素的影响。代表性实验的照片显示,血小板沿分化的内皮细胞黏附。向试验中添加α-凝血酶(0.1 - 1国际单位/毫升)、一氧化氮(NO)供体硝普钠(SNP;1 - 100微摩尔)或NO合酶抑制剂L - NG - 精氨酸甲酯(L - NAME,30 - 300微摩尔),与单独使用血小板相比,对管形成没有影响。神经氨酸酶(0.01国际单位 / 10⁷个血小板)可去除膜糖蛋白上的唾液酸残基,消除了血小板对管形成的促进作用。在存在经神经氨酸酶处理的血小板时,相对管面积为0.81±0.03(n = 8),在存在未处理的血小板时为1.69±0.09,P<0.001(n = 8),在不存在血小板时为0.80±0.04(n = 8)。抑制血管性血友病因子、纤维蛋白原和纤连蛋白介导的黏附的四肽Arg - Gly - Asp - Ser(RGDS;20 - 200微摩尔)对血小板对管形成的促进作用没有影响。这些结果表明血小板在体外促进血管生成。这种作用在很大程度上独立于α-凝血酶的激活,不受一氧化氮和前列腺素代谢调节的影响,可能通过血小板与分化的内皮细胞黏附来实现。

相似文献

1
Evidence that platelets promote tube formation by endothelial cells on matrigel.
Br J Pharmacol. 1998 Nov;125(6):1252-7. doi: 10.1038/sj.bjp.0702191.
3
Thrombin promotes endothelial cell alignment in Matrigel in vitro and angiogenesis in vivo.
Am J Physiol. 1997 Jul;273(1 Pt 1):C239-45. doi: 10.1152/ajpcell.1997.273.1.C239.
4
Cyclic strain disrupts endothelial network formation on Matrigel.
Microvasc Res. 2009 Dec;78(3):358-63. doi: 10.1016/j.mvr.2009.08.002. Epub 2009 Aug 18.
5
Caveolin-1 is important for nitric oxide-mediated angiogenesis in fibrin gels with human umbilical vein endothelial cells.
Acta Pharmacol Sin. 2006 Dec;27(12):1567-74. doi: 10.1111/j.1745-7254.2006.00462.x.
7
Differential role of platelet granular mediators in angiogenesis.
Cardiovasc Res. 2004 Aug 1;63(2):226-35. doi: 10.1016/j.cardiores.2004.04.012.
8
Ursolic acid mediates the vasorelaxant activity of Lepechinia caulescens via NO release in isolated rat thoracic aorta.
Life Sci. 2006 Aug 8;79(11):1062-8. doi: 10.1016/j.lfs.2006.03.006. Epub 2006 Apr 21.
9
Novel function of ascorbic acid as an angiostatic factor.
Angiogenesis. 2003;6(4):259-69. doi: 10.1023/B:AGEN.0000029390.09354.f8.

引用本文的文献

2
The prospects of microphysiological systems in modeling platelet pathophysiology in cancer.
Platelets. 2023 Dec;34(1):2247489. doi: 10.1080/09537104.2023.2247489.
3
The role of tumor-platelet interplay and micro tumor thrombi during hematogenous tumor metastasis.
Cell Oncol (Dordr). 2023 Jun;46(3):521-532. doi: 10.1007/s13402-023-00773-1. Epub 2023 Jan 18.
4
Platelets and (Lymph)angiogenesis.
Cold Spring Harb Perspect Med. 2023 Jan 3;13(1):a041174. doi: 10.1101/cshperspect.a041174.
6
Platelet-Cancer Interplay: Molecular Mechanisms and New Therapeutic Avenues.
Front Oncol. 2021 Jul 12;11:665534. doi: 10.3389/fonc.2021.665534. eCollection 2021.
7
Angiogenesis Is Differentially Modulated by Platelet-Derived Products.
Biomedicines. 2021 Mar 4;9(3):251. doi: 10.3390/biomedicines9030251.
8
The role of platelets in thrombus fibrosis and vessel wall remodeling after venous thrombosis.
J Thromb Haemost. 2021 Feb;19(2):387-399. doi: 10.1111/jth.15134. Epub 2020 Nov 29.
9
The Emerging Role of Platelets in the Formation of the Micrometastatic Niche: Current Evidence and Future Perspectives.
Front Oncol. 2020 Mar 18;10:374. doi: 10.3389/fonc.2020.00374. eCollection 2020.
10
Platelets and Immune Responses During Thromboinflammation.
Front Immunol. 2019 Jul 26;10:1731. doi: 10.3389/fimmu.2019.01731. eCollection 2019.

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