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本文引用的文献

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Engineered microvessels with strong alignment and high lumen density via cell-induced fibrin gel compaction and interstitial flow.通过细胞诱导的纤维蛋白凝胶压实和间质流实现具有强取向和高腔密度的工程化微血管。
Tissue Eng Part A. 2014 Feb;20(3-4):553-65. doi: 10.1089/ten.TEA.2013.0262. Epub 2013 Nov 14.
2
Aligned human microvessels formed in 3D fibrin gel by constraint of gel contraction.在 3D 纤维蛋白凝胶中,通过凝胶收缩的限制作用形成了排列整齐的人微血管。
Microvasc Res. 2013 Nov;90:12-22. doi: 10.1016/j.mvr.2013.07.010. Epub 2013 Aug 9.
3
In vitro perfused human capillary networks.在体人毛细血管网络灌流
Tissue Eng Part C Methods. 2013 Sep;19(9):730-7. doi: 10.1089/ten.TEC.2012.0430. Epub 2013 Feb 21.
4
Stromal cell identity influences the in vivo functionality of engineered capillary networks formed by co-delivery of endothelial cells and stromal cells.基质细胞特性影响内皮细胞和基质细胞共递送形成的工程化毛细血管网络的体内功能。
Tissue Eng Part A. 2013 May;19(9-10):1209-22. doi: 10.1089/ten.TEA.2012.0281. Epub 2013 Feb 1.
5
Tuning three-dimensional collagen matrix stiffness independently of collagen concentration modulates endothelial cell behavior.独立于胶原蛋白浓度调节三维胶原基质硬度可调节内皮细胞行为。
Acta Biomater. 2013 Jan;9(1):4635-44. doi: 10.1016/j.actbio.2012.08.007. Epub 2012 Aug 16.
6
Microstructural and mechanical differences between digested collagen-fibrin co-gels and pure collagen and fibrin gels.消化胶原-纤维蛋白共凝胶与纯胶原和纤维蛋白凝胶的微观结构和力学差异。
Acta Biomater. 2012 Nov;8(11):4031-42. doi: 10.1016/j.actbio.2012.07.010. Epub 2012 Jul 22.
7
High-purity enrichment of functional cardiovascular cells from human iPS cells.从人诱导多能干细胞中高效纯化成功能心血管细胞。
Cardiovasc Res. 2012 Aug 1;95(3):327-35. doi: 10.1093/cvr/cvs185. Epub 2012 Jun 6.
8
In vitro microvessels for the study of angiogenesis and thrombosis.用于研究血管生成和血栓形成的体外微血管。
Proc Natl Acad Sci U S A. 2012 Jun 12;109(24):9342-7. doi: 10.1073/pnas.1201240109. Epub 2012 May 29.
9
In vitro differentiation of bone marrow derived porcine mesenchymal stem cells to endothelial cells.骨髓来源猪间充质干细胞向血管内皮细胞的体外分化。
J Tissue Eng Regen Med. 2013 Nov;7(11):911-20. doi: 10.1002/term.1483. Epub 2012 May 18.
10
Plasma expanders stabilize human microvessels in microfluidic scaffolds.血浆扩容剂稳定微流控支架中的人微血管。
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纤维蛋白凝胶中的血管生成和血管发生的体外模型。

In vitro models of angiogenesis and vasculogenesis in fibrin gel.

机构信息

Departments of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.

出版信息

Exp Cell Res. 2013 Oct 1;319(16):2409-17. doi: 10.1016/j.yexcr.2013.06.006. Epub 2013 Jun 22.

DOI:10.1016/j.yexcr.2013.06.006
PMID:23800466
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3919069/
Abstract

In vitro models of endothelial assembly into microvessels are useful for the study of angiogenesis and vasculogenesis. In addition, such models may be used to provide the microvasculature required to sustain engineered tissues. A large range of in vitro models of both angiogenesis and vasculogenesis have utilized fibrin gel as a scaffold. Although fibrin gel is conducive to endothelial assembly, its ultrastructure varies substantially based on the gel formulation and gelation conditions, making it challenging to compare between models. This work reviews existing models of endothelial assembly in fibrin gel and posits that differerences between models are partially caused by microstructural differences in fibrin gel.

摘要

体外模型用于研究血管生成和血管发生。此外,此类模型可用于提供维持工程组织所需的微血管。大量的血管生成和血管发生的体外模型都利用纤维蛋白凝胶作为支架。尽管纤维蛋白凝胶有利于内皮细胞的组装,但它的超微结构因凝胶配方和凝胶条件的不同而有很大差异,这使得模型之间的比较变得具有挑战性。本文综述了纤维蛋白凝胶中内皮细胞组装的现有模型,并提出模型之间的差异部分是由于纤维蛋白凝胶的微观结构差异引起的。