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本文引用的文献

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Surfaces that sequester serum-borne heparin amplify growth factor activity.能结合血清中肝素的表面可放大生长因子的活性。
Adv Mater. 2011 Dec 1;23(45):5415-8. doi: 10.1002/adma.201103046. Epub 2011 Oct 26.
2
Biomaterials that regulate growth factor activity via bioinspired interactions.通过仿生相互作用调节生长因子活性的生物材料。
Adv Funct Mater. 2011 May 24;21(10):1754-1768. doi: 10.1002/adfm.201002468.
3
Harnessing endogenous growth factor activity modulates stem cell behavior.利用内源性生长因子活性调节干细胞行为。
Integr Biol (Camb). 2011 Aug;3(8):832-42. doi: 10.1039/c1ib00021g. Epub 2011 Jul 1.
4
[Ca2+]i signaling vs. eNOS expression as determinants of NO output in uterine artery endothelium: relative roles in pregnancy adaptation and reversal by VEGF165.钙离子信号与 eNOS 表达作为子宫动脉内皮细胞中 NO 输出的决定因素:VEGF165 在妊娠适应和逆转中的相对作用。
Am J Physiol Heart Circ Physiol. 2011 Apr;300(4):H1182-93. doi: 10.1152/ajpheart.01108.2010. Epub 2011 Jan 14.
5
Functional PEG-peptide hydrogels to modulate local inflammation induced by the pro-inflammatory cytokine TNFalpha.功能性聚乙二醇-肽水凝胶调节促炎细胞因子肿瘤坏死因子α诱导的局部炎症。
Biomaterials. 2009 Oct;30(28):4907-14. doi: 10.1016/j.biomaterials.2009.05.083. Epub 2009 Jun 27.
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Anti-VEGF therapy: comparison of current and future agents.抗血管内皮生长因子(VEGF)疗法:当前与未来药物的比较
Eye (Lond). 2008 Oct;22(10):1330-6. doi: 10.1038/eye.2008.88. Epub 2008 May 23.
7
Rationally designed peptides for controlled release of nerve growth factor from fibrin matrices.用于从纤维蛋白基质中控制释放神经生长因子的合理设计的肽。
J Biomed Mater Res A. 2007 Jan;80(1):13-23. doi: 10.1002/jbm.a.30844.
8
Heparin-regulated release of growth factors in vitro and angiogenic response in vivo to implanted hyaluronan hydrogels containing VEGF and bFGF.肝素调节生长因子的体外释放以及体内对植入含血管内皮生长因子(VEGF)和碱性成纤维细胞生长因子(bFGF)的透明质酸水凝胶的血管生成反应。
Biomaterials. 2006 Oct;27(30):5242-51. doi: 10.1016/j.biomaterials.2006.05.018. Epub 2006 Jun 30.
9
Potent inhibition of angiogenesis by D,L-peptides derived from vascular endothelial growth factor receptor 2.源自血管内皮生长因子受体2的D,L-肽对血管生成的强效抑制作用
Thromb Haemost. 2003 Sep;90(3):501-10. doi: 10.1160/TH03-02-0106.
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The biology of VEGF and its receptors.血管内皮生长因子(VEGF)及其受体的生物学特性
Nat Med. 2003 Jun;9(6):669-76. doi: 10.1038/nm0603-669.

利用固定化支化配体调节特定生长因子信号。

Regulating specific growth factor signaling using immobilized branched ligands.

机构信息

Departments of Biomedical Engineering and Orthopedics & Rehabilitation, University of Wisconsin, 5009 Wisconsin Institutes of Medical Research, 1111 Highland Ave., Madison, WI 53705, USA.

出版信息

Adv Healthc Mater. 2012 Jul;1(4):457-60. doi: 10.1002/adhm.201200077. Epub 2012 May 11.

DOI:10.1002/adhm.201200077
PMID:23184776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3925890/
Abstract

VEGF-binding peptide ligands are incorporated into hydrogel microspheres and reduce the amount of growth factor in solution. VEGF binding affinity is enhanced by creating ligands with a dimer structure. The spheres are able to knock down VEGF-mediated HUVEC growth and reduce calcium signaling. The binding interaction is reversible, allowing the spheres to be used as a VEGF delivery vehicle.

摘要

VEGF 结合肽配体被整合到水凝胶微球中,从而减少溶液中生长因子的含量。通过构建具有二聚体结构的配体可以增强 VEGF 结合亲和力。这些球体能够抑制 VEGF 介导的 HUVEC 生长并减少钙信号转导。结合相互作用是可逆的,允许球体用作 VEGF 递送载体。