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本文引用的文献

1
Computer-Aided Patient-Specific Coronary Artery Graft Design Improvements Using CFD Coupled Shape Optimizer.使用计算流体动力学耦合形状优化器的计算机辅助特定患者冠状动脉移植设计改进
Cardiovasc Eng Technol. 2011 Mar;2(1):35-47. doi: 10.1007/s13239-010-0029-z. Epub 2010 Nov 18.
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Analysis of early embryonic great-vessel microcirculation in zebrafish using high-speed confocal μPIV.使用高速共聚焦微粒子图像测速技术分析斑马鱼早期胚胎大血管微循环。
Biorheology. 2011;48(5):305-21. doi: 10.3233/BIR-2012-0600.
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Kinematics of cardiac growth: in vivo characterization of growth tensors and strains.心脏生长的运动学:生长张量和应变的体内特征化。
J Mech Behav Biomed Mater. 2012 Apr;8:165-77. doi: 10.1016/j.jmbbm.2011.12.006. Epub 2011 Dec 24.
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Computational hemodynamic optimization predicts dominant aortic arch selection is driven by embryonic outflow tract orientation in the chick embryo.计算血流动力学优化预测主导主动脉弓的选择是由鸡胚胚胎流出道的方向决定的。
Biomech Model Mechanobiol. 2012 Sep;11(7):1057-73. doi: 10.1007/s10237-012-0373-z. Epub 2012 Feb 4.
5
Site-specific microRNA-92a regulation of Kruppel-like factors 4 and 2 in atherosusceptible endothelium.靶向 microRNA-92a 调控易损性血管内皮 Kruppel 样因子 4 和 2。
Arterioscler Thromb Vasc Biol. 2012 Apr;32(4):979-87. doi: 10.1161/ATVBAHA.111.244053. Epub 2012 Jan 19.
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In vivo shear stress response.体内切应力响应。
Biochem Soc Trans. 2011 Dec;39(6):1633-8. doi: 10.1042/BST20110715.
7
Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis.先天性心脏病的全球出生患病率:系统评价和荟萃分析。
J Am Coll Cardiol. 2011 Nov 15;58(21):2241-7. doi: 10.1016/j.jacc.2011.08.025.
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A blood flow-dependent klf2a-NO signaling cascade is required for stabilization of hematopoietic stem cell programming in zebrafish embryos.血流依赖的 klf2a-NO 信号级联反应对于斑马鱼胚胎造血干细胞编程的稳定是必需的。
Blood. 2011 Oct 13;118(15):4102-10. doi: 10.1182/blood-2011-05-353235. Epub 2011 Aug 17.
9
Heparan sulfate proteoglycan mediates shear stress-induced endothelial gene expression in mouse embryonic stem cell-derived endothelial cells.硫酸乙酰肝素蛋白聚糖介导剪切应力诱导的小鼠胚胎干细胞来源的内皮细胞中内皮基因的表达。
Biotechnol Bioeng. 2012 Feb;109(2):583-94. doi: 10.1002/bit.23302. Epub 2011 Aug 31.
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Dynamic molecular processes mediate cellular mechanotransduction.动态分子过程介导细胞力学转导。
Nature. 2011 Jul 20;475(7356):316-23. doi: 10.1038/nature10316.

胚胎血管发育中的力学转导。

Mechanotransduction in embryonic vascular development.

机构信息

Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Biomech Model Mechanobiol. 2012 Nov;11(8):1149-68. doi: 10.1007/s10237-012-0412-9. Epub 2012 Jun 29.

DOI:10.1007/s10237-012-0412-9
PMID:22744845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4502581/
Abstract

A plethora of biochemical signals provides spatial and temporal cues that carefully orchestrate the complex process of vertebrate embryonic development. The embryonic vasculature develops not only in the context of these biochemical cues, but also in the context of the biomechanical forces imparted by blood flow. In the mature vasculature, different blood flow regimes induce distinct genetic programs, and significant progress has been made toward understanding how these forces are perceived by endothelial cells and transduced into biochemical signals. However, it cannot be assumed that paradigms that govern the mature vasculature are pertinent to the developing embryonic vasculature. The embryonic vasculature can respond to the mechanical forces of blood flow, and these responses are critical in vascular remodeling, certain aspects of sprouting angiogenesis, and maintenance of arterial-venous identity. Here, we review data regarding mechanistic aspects of endothelial cell mechanotransduction, with a focus on the response to shear stress, and elaborate upon the multifarious effects of shear stress on the embryonic vasculature. In addition, we discuss emerging predictive vascular growth models and highlight the prospect of combining signaling pathway information with computational modeling. We assert that correlation of precise measurements of hemodynamic parameters with effects on endothelial cell gene expression and cell behavior is required for fully understanding how blood flow-induced loading governs normal vascular development and shapes congenital cardiovascular abnormalities.

摘要

大量的生化信号提供了时空线索,精心协调了脊椎动物胚胎发育的复杂过程。胚胎脉管系统不仅在这些生化信号的背景下发育,而且还在血流施加的生物力学力的背景下发育。在成熟的脉管系统中,不同的血流模式会诱导不同的遗传程序,并且在理解这些力如何被内皮细胞感知并转化为生化信号方面已经取得了重大进展。然而,不能假设支配成熟脉管系统的范例与正在发育的胚胎脉管系统有关。胚胎脉管系统可以对血流的机械力作出反应,这些反应在血管重塑、某些发芽血管生成方面以及维持动静脉特征方面至关重要。在这里,我们回顾了关于内皮细胞力学转导的机制方面的数据,重点是对切应力的反应,并详细阐述了切应力对胚胎脉管系统的多方面影响。此外,我们讨论了新兴的预测性血管生长模型,并强调了将信号通路信息与计算模型相结合的前景。我们断言,需要将精确测量的血液动力学参数与对内皮细胞基因表达和细胞行为的影响进行相关联,才能充分了解血流诱导的负荷如何控制正常血管发育并塑造先天性心血管异常。