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2
Reorganization of basement membrane matrices by cellular traction promotes the formation of cellular networks in vitro.细胞牵引力对基底膜基质的重组促进体外细胞网络的形成。
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Cell directional persistence [corrected] and chemotaxis in vascular morphogenesis.细胞定向持久性[已修正]与血管形态发生中的趋化作用。
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本文引用的文献

1
Percolation, morphogenesis, and burgers dynamics in blood vessels formation.血管形成中的渗流、形态发生和伯格斯动力学。
Phys Rev Lett. 2003 Mar 21;90(11):118101. doi: 10.1103/PhysRevLett.90.118101. Epub 2003 Mar 17.
2
Spatially restricted patterning cues provided by heparin-binding VEGF-A control blood vessel branching morphogenesis.由肝素结合型血管内皮生长因子A提供的空间受限的模式线索控制血管分支形态发生。
Genes Dev. 2002 Oct 15;16(20):2684-98. doi: 10.1101/gad.242002.
3
Vascular abnormalities and deregulation of VEGF in Lkb1-deficient mice.Lkb1基因缺陷小鼠的血管异常与血管内皮生长因子(VEGF)失调
Science. 2001 Aug 17;293(5533):1323-6. doi: 10.1126/science.1062074.
4
Phase transition between disordered and ordered foraging in Pharaoh's ants.法老蚁无序觅食与有序觅食之间的相变
Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9703-6. doi: 10.1073/pnas.161285298. Epub 2001 Aug 7.
5
A computational study of the effect of vasomotion on oxygen transport from capillary networks.血管运动对毛细血管网络氧输送影响的计算研究。
J Theor Biol. 2001 Mar 21;209(2):189-99. doi: 10.1006/jtbi.2000.2254.
6
Angiomotin: an angiostatin binding protein that regulates endothelial cell migration and tube formation.
J Cell Biol. 2001 Mar 19;152(6):1247-54. doi: 10.1083/jcb.152.6.1247.
7
IL-12 inhibition of endothelial cell functions and angiogenesis depends on lymphocyte-endothelial cell cross-talk.白细胞介素-12对内皮细胞功能和血管生成的抑制作用取决于淋巴细胞与内皮细胞之间的相互作用。
J Immunol. 2001 Mar 15;166(6):3890-9. doi: 10.4049/jimmunol.166.6.3890.
8
The role of FGF and VEGF in angioblast induction and migration during vascular development.成纤维细胞生长因子(FGF)和血管内皮生长因子(VEGF)在血管发育过程中对成血管细胞诱导和迁移的作用。
Dev Dyn. 2001 Jan;220(1):1-17. doi: 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1087>3.0.CO;2-2.
9
The control of chemotactic cell movement during Dictyostelium morphogenesis.盘基网柄菌形态发生过程中趋化性细胞运动的控制
Philos Trans R Soc Lond B Biol Sci. 2000 Jul 29;355(1399):983-91. doi: 10.1098/rstb.2000.0634.
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Building the vertebrate vasculature: research is going swimmingly.
Bioessays. 2000 Oct;22(10):882-93. doi: 10.1002/1521-1878(200010)22:10<882::AID-BIES3>3.0.CO;2-J.

模拟血管网络组装的早期阶段。

Modeling the early stages of vascular network assembly.

作者信息

Serini Guido, Ambrosi Davide, Giraudo Enrico, Gamba Andrea, Preziosi Luigi, Bussolino Federico

机构信息

Institute for Cancer Research and Treatment and Department of Oncological Sciences, University of Torino, 10060 Candiolo (TO).

出版信息

EMBO J. 2003 Apr 15;22(8):1771-9. doi: 10.1093/emboj/cdg176.

DOI:10.1093/emboj/cdg176
PMID:12682010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC154468/
Abstract

In vertebrates, networks of capillary vessels supply tissues with nutrients. Capillary patterns are closely mimicked by endothelial cells cultured on basement membrane proteins that allow single randomly dispersed cells to self-organize into vascular networks. Here we provide a model including chemoattraction as the fundamental mechanism for cell-to-cell communication in order to identify key parameters in the complexity of the formation of vascular patterns. By flanking biological experiments, theoretical insights and numerical simulations, we provide strong evidence that endothelial cell number and the range of activity of a chemoattractant factor regulate vascular network formation and size. We propose a mechanism linking the scale of formed endothelial structures to the range of cell-to-cell interaction mediated by the release of chemoattractants.

摘要

在脊椎动物中,毛细血管网络为组织提供营养。在基底膜蛋白上培养的内皮细胞能紧密模拟毛细血管模式,这些基底膜蛋白可使单个随机分散的细胞自组织形成血管网络。在此,我们提供了一个模型,该模型将化学吸引作为细胞间通讯的基本机制,以确定血管模式形成复杂性中的关键参数。通过结合生物学实验、理论见解和数值模拟,我们提供了有力证据,证明内皮细胞数量和化学吸引因子的活性范围调节血管网络的形成和大小。我们提出了一种机制,将形成的内皮结构的规模与由化学吸引剂释放介导的细胞间相互作用范围联系起来。