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胶原基质物理特性调节体内内皮祖细胞衍生的血管。

Collagen matrix physical properties modulate endothelial colony forming cell-derived vessels in vivo.

机构信息

Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.

出版信息

Microvasc Res. 2010 Jul;80(1):23-30. doi: 10.1016/j.mvr.2010.03.001. Epub 2010 Mar 8.

Abstract

Developing tissue engineering approaches to generate functional vascular networks is important for improving treatments of peripheral and cardiovascular disease. Endothelial colony forming cells (ECFCs) are an endothelial progenitor cell (EPC) population defined by high proliferative potential and an ability to vascularize collagen-based matrices in vivo. Little is known regarding how physical properties of the local cell microenvironment guide vessel formation following EPC transplantation. In vitro evidence suggests that collagen matrix stiffness may modulate EPC vessel formation. The present study determined the ability of 3D collagen matrix physical properties, varied by changing collagen concentration, to influence ECFC vasculogenesis in vivo. Human umbilical cord blood ECFCs were cultured within matrices for 18 h in vitro and then fixed for in vitro analysis or implanted subcutaneously into the flank of immunodeficient mice for 14 days. We report that increasing collagen concentration significantly decreased ECFC derived vessels per area (density), but significantly increased vessel sizes (total cross sectional area). These results demonstrate that the physical properties of collagen matrices influence ECFC vasculogenesis in vivo and that by modulating these properties, one can guide vascularization.

摘要

开发组织工程方法来生成功能性血管网络对于改善外周血管和心血管疾病的治疗非常重要。内皮祖细胞 (EPC) 是一类内皮细胞前体细胞 (EPC),其特征是具有高增殖潜力和在体内使基于胶原蛋白的基质血管化的能力。关于局部细胞微环境的物理特性如何在 EPC 移植后指导血管形成,目前知之甚少。体外证据表明,胶原蛋白基质的硬度可能调节 EPC 血管形成。本研究确定了通过改变胶原蛋白浓度来改变 3D 胶原蛋白基质物理特性的能力,从而在体内影响 ECFC 血管生成。人脐血 ECFC 在体外培养 18 小时后,在体外进行固定分析或植入免疫缺陷小鼠的侧腹 14 天。我们报告说,胶原蛋白浓度的增加显著降低了单位面积(密度)的 ECFC 衍生血管,但显著增加了血管大小(总横截面积)。这些结果表明,胶原蛋白基质的物理特性会影响体内 ECFC 的血管生成,并且通过调节这些特性,可以指导血管化。

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