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用于增强雪旺细胞存活及控制三维细胞形态的I型胶原蛋白-基质胶支架

Collagen I-matrigel scaffolds for enhanced Schwann cell survival and control of three-dimensional cell morphology.

作者信息

Dewitt Daniel D, Kaszuba Stephanie N, Thompson Deanna M, Stegemann Jan P

机构信息

Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York, USA.

出版信息

Tissue Eng Part A. 2009 Oct;15(10):2785-93. doi: 10.1089/ten.TEA.2008.0406.

DOI:10.1089/ten.TEA.2008.0406
PMID:19231925
Abstract

We report on the ability to control three-dimensional Schwann cell (SC) morphology using collagen I-Matrigel composite scaffolds for neural engineering applications. SCs are supportive of nerve regeneration after injury, and it has recently been reported that SCs embedded in collagen I, a material frequently used in guidance channel studies, do not readily extend processes, instead adopting a spherical morphology indicative of little interaction with the matrix. We have modified collagen I matrices by adding Matrigel to make them more supportive of SCs and characterized these matrices and SC morphology in vitro. Incorporation of 10%, 20%, 35%, and 50% Matrigel by volume resulted in 2.4, 3.5, 3.7, and 4.2 times longer average SC process length after 14 days in culture than with collagen I-only controls. Additionally, only 35% and 50% Matrigel constructs were able to maintain SC number over 14 days, whereas an 88% decrease in cells from initial seeding density was observed in collagen-only constructs over the same time period. Mechanical testing revealed that the addition of 50% Matrigel increased matrix stiffness from 6.4 kPa in collagen I-only constructs to 9.8 kPa. Furthermore, second harmonic generation imaging showed that the addition of Matrigel resulted in non-uniform distribution of collagen I, and scanning electron microscope imaging illustrated distinct differences in the fibrillar structure of the different constructs. Collectively, this work lays a foundation for developing scaffolding materials that are concurrently supportive of neurons and SCs for future neural engineering applications.

摘要

我们报告了使用I型胶原-基质胶复合支架来控制三维雪旺细胞(SC)形态以用于神经工程应用的能力。雪旺细胞有助于损伤后的神经再生,最近有报道称,嵌入I型胶原(一种在引导通道研究中常用的材料)中的雪旺细胞不容易伸出突起,而是呈现球形形态,这表明与基质的相互作用很少。我们通过添加基质胶对I型胶原基质进行了改良,使其更有利于雪旺细胞生长,并在体外对这些基质和雪旺细胞形态进行了表征。按体积加入10%、20%、35%和50%的基质胶后,培养14天后雪旺细胞突起的平均长度分别是仅使用I型胶原作为对照时的2.4倍、3.5倍、3.7倍和4.2倍。此外,只有含35%和50%基质胶的构建体能够在14天内维持雪旺细胞数量,而在同一时间段内,仅含胶原的构建体中细胞数量从初始接种密度下降了88%。力学测试表明,添加50%的基质胶使基质硬度从仅含I型胶原构建体的6.4 kPa增加到9.8 kPa。此外,二次谐波生成成像显示添加基质胶导致I型胶原分布不均匀,扫描电子显微镜成像表明不同构建体的纤维结构存在明显差异。总的来说,这项工作为开发同时支持神经元和雪旺细胞的支架材料奠定了基础,以用于未来的神经工程应用。

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