Decellularized matrix bioink with gelatin methacrylate for simultaneous improvements in printability and biofunctionality

去细胞化 明胶 甲基丙烯酸酯 活力测定 自愈水凝胶 细胞外基质 基质(化学分析) 组织工程 3D生物打印 再生(生物学) 材料科学 化学 细胞 生物医学工程 聚合物 复合材料 高分子化学 细胞生物学 生物化学 聚合 生物 医学
作者
Ji Min Seok,Minjun Ahn,Dahong Kim,Jae‐Seong Lee,Dongjin Lee,Min-Ju Choi,Seon Ju Yeo,Jun Hee Lee,Kangwon Lee,Byoung Soo Kim,Su A Park
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:262 (Pt 2): 130194-130194 被引量:9
标识
DOI:10.1016/j.ijbiomac.2024.130194
摘要

Gelatin methacrylate (GelMA) bioink has been widely used in bioprinting because it is a printable and biocompatible biomaterial. However, it is difficult to print GelMA bioink without any temperature control because it has a thermally-sensitive rheological property. Therefore, in this study, we developed a temperature-controlled printing system in real time without affecting the viability of the cells encapsulated in the bioink. In addition, a skin-derived decellularized extracellular matrix (SdECM) was printed with GelMA to better mimic the native tissue environment compared with solely using GelMA bioink with the enhancement of structural stability. The temperature setting accuracy was calculated to be 98.58 ± 1.8 % for the module and 99.48 ± 1.33 % for the plate from 5 °C to 37 °C. The group of the temperature of the module at 10 °C and the plate at 20 °C have 93.84 % cell viability with the printable range in the printability window. In particular, the cell viability and proliferation were increased in the encapsulated fibroblasts in the GelMA/SdECM bioink, relative to the GelMA bioink, with a morphology that significantly spread for seven days. The gene expression and growth factors related to skin tissue regeneration were relatively upregulated with SdECM components. In the bioprinting process, the rheological properties of the GelMA/SdECM bioink were successfully adjusted in real time to increase printability, and the native skin tissue mimicked components providing tissue-specific biofunctions to the encapsulated cells. The developed bioprinting strategies and bioinks could support future studies related to the skin tissue reconstruction, regeneration, and other medical applications using the bioprinting process.
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