• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Jostling for position in angiogenic sprouts: continuous rearrangement of cells explained by differential adhesion dynamics.血管生成芽中争夺位置:通过差异粘附动力学解释细胞的连续重排。
EMBO J. 2014 May 16;33(10):1089-90. doi: 10.1002/embj.201488452. Epub 2014 Apr 7.
2
The role of differential VE-cadherin dynamics in cell rearrangement during angiogenesis.血管生成过程中细胞重排中差异 VE-钙黏蛋白动力学的作用。
Nat Cell Biol. 2014 Apr;16(4):309-21. doi: 10.1038/ncb2926. Epub 2014 Mar 23.
3
Differential adhesion drives angiogenesis.差异黏附驱动血管生成。
Nat Cell Biol. 2014 Apr;16(4):305-6. doi: 10.1038/ncb2943.
4
Glycolytic regulation of cell rearrangement in angiogenesis.糖酵解调控血管生成中的细胞重排。
Nat Commun. 2016 Jul 20;7:12240. doi: 10.1038/ncomms12240.
5
The Force at the Tip--Modelling Tension and Proliferation in Sprouting Angiogenesis.尖端的力——模拟发芽血管生成中的张力与增殖
PLoS Comput Biol. 2015 Aug 6;11(8):e1004436. doi: 10.1371/journal.pcbi.1004436. eCollection 2015 Aug.
6
Polarized actin and VE-cadherin dynamics regulate junctional remodelling and cell migration during sprouting angiogenesis.极化的肌动蛋白和 VE-钙黏蛋白动态调节芽生血管生成过程中的连接重塑和细胞迁移。
Nat Commun. 2017 Dec 20;8(1):2210. doi: 10.1038/s41467-017-02373-8.
7
Intermedin: a novel regulator for vascular remodeling and tumor vessel normalization by regulating vascular endothelial-cadherin and extracellular signal-regulated kinase.中介素:通过调节血管内皮钙黏蛋白和细胞外信号调节激酶来调节血管重塑和肿瘤血管正常化的新型调节剂。
Arterioscler Thromb Vasc Biol. 2012 Nov;32(11):2721-32. doi: 10.1161/ATVBAHA.112.300185. Epub 2012 Aug 23.
8
Tipping the balance: robustness of tip cell selection, migration and fusion in angiogenesis.打破平衡:血管生成中尖端细胞选择、迁移和融合的稳健性。
PLoS Comput Biol. 2009 Oct;5(10):e1000549. doi: 10.1371/journal.pcbi.1000549. Epub 2009 Oct 30.
9
Dynamics of endothelial cell behavior in sprouting angiogenesis.血管生成中内皮细胞行为的动力学。
Curr Opin Cell Biol. 2010 Oct;22(5):617-25. doi: 10.1016/j.ceb.2010.08.010.
10
Time to Decide? Dynamical Analysis Predicts Partial Tip/Stalk Patterning States Arise during Angiogenesis.是时候做决定了?动力学分析预测血管生成过程中会出现部分尖端/柄部模式状态。
PLoS One. 2016 Nov 15;11(11):e0166489. doi: 10.1371/journal.pone.0166489. eCollection 2016.

引用本文的文献

1
Cgnl1, an endothelial junction complex protein, regulates GTPase mediated angiogenesis.Cgnl1,一种血管内皮细胞连接复合物蛋白,调节 GTPase 介导的血管生成。
Cardiovasc Res. 2017 Dec 1;113(14):1776-1788. doi: 10.1093/cvr/cvx175.

本文引用的文献

1
The role of differential VE-cadherin dynamics in cell rearrangement during angiogenesis.血管生成过程中细胞重排中差异 VE-钙黏蛋白动力学的作用。
Nat Cell Biol. 2014 Apr;16(4):309-21. doi: 10.1038/ncb2926. Epub 2014 Mar 23.
2
In vivo analysis reveals a highly stereotypic morphogenetic pathway of vascular anastomosis.体内分析揭示了血管吻合的高度刻板形态发生途径。
Dev Cell. 2013 Jun 10;25(5):492-506. doi: 10.1016/j.devcel.2013.05.010.
3
The tip cell concept 10 years after: new players tune in for a common theme.十年后的顶端细胞概念:新参与者融入共同主题。
Exp Cell Res. 2013 May 15;319(9):1255-63. doi: 10.1016/j.yexcr.2013.01.019. Epub 2013 Feb 16.
4
Angiogenic morphogenesis driven by dynamic and heterogeneous collective endothelial cell movement.由动态和异质的集体内皮细胞运动驱动的血管生成形态发生。
Development. 2011 Nov;138(21):4763-76. doi: 10.1242/dev.068023. Epub 2011 Sep 28.
5
Basic and therapeutic aspects of angiogenesis.血管生成的基础与治疗方面。
Cell. 2011 Sep 16;146(6):873-87. doi: 10.1016/j.cell.2011.08.039.
6
Spatial regulation of Dia and Myosin-II by RhoGEF2 controls initiation of E-cadherin endocytosis during epithelial morphogenesis.RhoGEF2 通过调控 Dia 和肌球蛋白-II 的空间分布来控制上皮形态发生过程中 E-钙黏蛋白内吞作用的起始。
Nat Cell Biol. 2011 May;13(5):529-40. doi: 10.1038/ncb2224. Epub 2011 Apr 24.
7
Endothelial cells dynamically compete for the tip cell position during angiogenic sprouting.内皮细胞在血管生成芽生过程中动态竞争尖端细胞位置。
Nat Cell Biol. 2010 Oct;12(10):943-53. doi: 10.1038/ncb2103. Epub 2010 Sep 26.
8
Tipping the balance: robustness of tip cell selection, migration and fusion in angiogenesis.打破平衡:血管生成中尖端细胞选择、迁移和融合的稳健性。
PLoS Comput Biol. 2009 Oct;5(10):e1000549. doi: 10.1371/journal.pcbi.1000549. Epub 2009 Oct 30.
9
Delta-like ligand 4 (Dll4) is induced by VEGF as a negative regulator of angiogenic sprouting.Delta样配体4(Dll4)由血管内皮生长因子(VEGF)诱导产生,作为血管生成芽的负调节因子。
Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3219-24. doi: 10.1073/pnas.0611206104. Epub 2007 Feb 12.
10
Dll4 signalling through Notch1 regulates formation of tip cells during angiogenesis.通过Notch1的Dll4信号传导在血管生成过程中调节顶端细胞的形成。
Nature. 2007 Feb 15;445(7129):776-80. doi: 10.1038/nature05571. Epub 2007 Jan 28.

血管生成芽中争夺位置:通过差异粘附动力学解释细胞的连续重排。

Jostling for position in angiogenic sprouts: continuous rearrangement of cells explained by differential adhesion dynamics.

机构信息

Wyss Institute for Biologically Inspired Engineering Harvard University, Boston, MA, USA Department of Biomedical Engineering, Boston University, Boston, MA, USA.

出版信息

EMBO J. 2014 May 16;33(10):1089-90. doi: 10.1002/embj.201488452. Epub 2014 Apr 7.

DOI:10.1002/embj.201488452
PMID:24711516
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4193916/
Abstract

Endothelial sprouting during angiogenesis is a highly coordinated morphogenetic process that involves polarized tip cells leading stalk cells to form new capillaries. While tip and stalk cells previously were thought to be stable and have static phenotypes within the sprout, it is becoming increasingly clear that endothelial cells undergo dynamic rearrangements. A new study using computer simulations, validated by in vitro and in vivo experimental data, now provides an explanation for these rearrangements, showing that sprouting cells are in a continuum of migratory states, regulated by differential cell-cell adhesions and protrusive activities to drive proper vascular organization.

摘要

血管生成过程中的血管内皮细胞发芽是一个高度协调的形态发生过程,涉及极化的尖端细胞引导衬里细胞形成新的毛细血管。虽然以前认为尖端和衬里细胞在芽中是稳定的,并且具有静态表型,但越来越明显的是,内皮细胞会发生动态重排。一项新的研究使用计算机模拟,并通过体外和体内实验数据进行验证,现在为这些重排提供了一个解释,表明发芽细胞处于迁移状态的连续体中,受细胞-细胞黏附差异和突起活动的调节,以驱动血管的正确组织。