在静态和动态生长条件下,多孔的原体支架使体内皮质光体在体外形成
Lena Rössler1,2, Ramin Nasehi1,3, Nadja Hansen1
1Department of Dental Materials and Biomaterials Research, RWTH Aachen University Hospital, Aachen, Germany.
概括
这项研究提出了一个3D原基架,使内皮细胞能够自组装成类似血管的结构,这对于组织工程至关重要. 该系统支持体外血管化,独立于动态流量条件.
科学领域:
- 生物材料科学 生物材料科学
- 组织工程是组织工程.
- 细胞生物学 细胞生物学
背景情况:
- 开发复杂的体外组织模型受到功能性血管系统缺失的阻碍.
- 整合血管对于工程组织中的营养/废物交换至关重要.
研究的目的:
- 开发一个三维中等尺度的体外血管化结合组织模型.
- 在这个模型中,研究内皮细胞的自我组装成类似血管的结构.
- 评估 perfusion 对细胞组织和血管形成的影响.
主要方法:
- 在原体支架中培养人类脉内皮细胞 (HUVEC) 和人类前皮纤维细胞.
- 使用定制的生物反应器进行 perfusion.
- 采用免疫光染色,双光子显微镜,第二和生成成像和扫描电子显微镜进行可视化.
主要成果:
- 证明了用于体外血管化的3D多孔原体支架系统的可行性.
- 观察到HUVEC的自我组装成空洞的,类似容器的结构.
- 在静态和动态 (透) 条件下确认了类似容器的结构形成.
结论:
- 开发的3D原基架系统有效地支持内皮细胞自我组织成血管状结构.
- 血管化可以实现独立于动态流动,简化了体外模型的开发.
- 这个模型为推进组织工程和再生医学提供了一个有前途的平台.
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