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评价不同孔径的 3D 打印明胶基支架用于 MSC 脂肪组织工程。

Evaluation of 3D Printed Gelatin-Based Scaffolds with Varying Pore Size for MSC-Based Adipose Tissue Engineering.

机构信息

Polymer Chemistry & Biomaterials Group, Centre of Macromolecular Chemistry (CMaC), Ghent University, Krijgslaan 281, S4-Bis, 9000, Ghent, Belgium.

Brussels Photonics, Vrije Universiteit Brussel, Pleinlaan 2, 1050, Brussels, Belgium.

出版信息

Macromol Biosci. 2020 Apr;20(4):e1900364. doi: 10.1002/mabi.201900364. Epub 2020 Feb 20.

Abstract

Adipose tissue engineering aims to provide solutions to patients who require tissue reconstruction following mastectomies or other soft tissue trauma. Mesenchymal stromal cells (MSCs) robustly differentiate into the adipogenic lineage and are attractive candidates for adipose tissue engineering. This work investigates whether pore size modulates adipogenic differentiation of MSCs toward identifying optimal scaffold pore size and whether pore size modulates spatial infiltration of adipogenically differentiated cells. To assess this, extrusion-based 3D printing is used to fabricate photo-crosslinkable gelatin-based scaffolds with pore sizes in the range of 200-600 µm. The adipogenic differentiation of MSCs seeded onto these scaffolds is evaluated and robust lipid droplet formation is observed across all scaffold groups as early as after day 6 of culture. Expression of adipogenic genes on scaffolds increases significantly over time, compared to TCP controls. Furthermore, it is found that the spatial distribution of cells is dependent on the scaffold pore size, with larger pores leading to a more uniform spatial distribution of adipogenically differentiated cells. Overall, these data provide first insights into the role of scaffold pore size on MSC-based adipogenic differentiation and contribute toward the rational design of biomaterials for adipose tissue engineering in 3D volumetric spaces.

摘要

脂肪组织工程旨在为接受乳房切除术或其他软组织创伤后的组织重建的患者提供解决方案。间充质基质细胞(MSCs)可强有力地向脂肪生成谱系分化,是脂肪组织工程的理想候选细胞。本研究旨在探讨孔径是否能调节 MSCs 的脂肪生成分化,以确定最佳支架孔径,以及孔径是否能调节脂肪生成分化细胞的空间浸润。为了评估这一点,使用挤出式 3D 打印技术制造孔径范围在 200-600μm 的光交联明胶基支架。将 MSCs 接种到这些支架上,评估其脂肪生成分化,结果在培养第 6 天即可观察到所有支架组中均出现大量的脂滴形成。与 TCP 对照组相比,支架上的脂肪生成基因表达随时间显著增加。此外,还发现细胞的空间分布依赖于支架的孔径,较大的孔径导致脂肪生成分化细胞的空间分布更加均匀。总的来说,这些数据首次提供了关于支架孔径对基于 MSC 的脂肪生成分化的作用的见解,并为 3D 体积空间中脂肪组织工程的生物材料的合理设计做出了贡献。

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