Department of Clinical Dentistry, University of Bergen, Bergen, Norway.
These authors contributed equally to the study.
Biomed Mater. 2021 Mar 5;16(3). doi: 10.1088/1748-605X/abe6d9.
A promising alternative to current treatment options for degenerative conditions of the temporomandibular joint (TMJ) is cartilage tissue engineering, using 3D printed scaffolds and mesenchymal stem cells. Gelatin, with its inherent biocompatibility and printability has been proposed as a scaffold biomaterial, but because of its thermoreversible properties, rapid degradation and inadequate strength it must be crosslinked to be stable in physiological conditions. The aim of this study was to identify non-toxic and effective crosslinking methods intended to improve the physical properties of 3D printed gelatin scaffolds for cartilage regeneration. Dehydrothermal (DHT), ribose glycation and dual crosslinking with both DHT and ribose treatments were tested. The crosslinked scaffolds were characterized by chemical, mechanical, and physical analysis. The dual-crosslinked scaffolds had the highest degree of crosslinking and the greatest resistance to hydrolytic and enzymatic degradation. Compared to the dual-crosslinked group, the ribose-crosslinked scaffolds had thinner printed strands, larger pore surface area and higher fluid uptake. The compressive modulus values were 2 kPa for ribose, 37.6 kPa for DHT and 30.9 kPa for dual-crosslinked scaffolds. None of the crosslinking methods had cytotoxic effects on the seeded rat bone marrow-derived mesenchymal stem cells (rBMSC). After 4 and 7 d, the dual-crosslinked scaffolds exhibited better cell proliferation than the other groups. Although all scaffolds supported chondrogenic differentiation of rBMSC, dual-crosslinked scaffolds demonstrated the lowest expression of the hypertrophy-related collagen 10 gene after 21 d. The results show that 3D printed gelatin scaffolds, when dually crosslinked with ribose and DHT methods, are not toxic, promote chondrogenic differentiation of rBMSC and have potential application in tissue engineering of TMJ condylar cartilage.
一种有前途的替代当前治疗颞下颌关节(TMJ)退行性疾病的方法是软骨组织工程,使用 3D 打印支架和间充质干细胞。明胶具有固有生物相容性和可打印性,已被提议作为支架生物材料,但由于其热可逆性质、快速降解和不足的强度,必须交联才能在生理条件下稳定。本研究的目的是确定非毒性和有效的交联方法,旨在改善用于软骨再生的 3D 打印明胶支架的物理性质。测试了脱水热(DHT)、核糖糖基化和 DHT 与核糖双重交联。交联支架通过化学、机械和物理分析进行了表征。双交联支架的交联度最高,对水解释和酶降解的抵抗力最大。与双交联组相比,核糖交联支架的打印丝更细,孔表面面积更大,吸水率更高。压缩模量值为核糖 2 kPa、DHT 37.6 kPa 和双交联支架 30.9 kPa。交联方法对接种的大鼠骨髓间充质干细胞(rBMSC)均无细胞毒性作用。在 4 和 7 d 时,双交联支架的细胞增殖优于其他组。尽管所有支架都支持 rBMSC 的软骨分化,但在 21 d 时,双交联支架表现出最低的肥大相关胶原 10 基因表达。结果表明,当用核糖和 DHT 方法双重交联 3D 打印明胶支架时,无毒,促进 rBMSC 的软骨分化,在 TMJ 髁突软骨组织工程中有潜在的应用。