基于改性丝素和明胶的生物相容性水凝胶微球用于可注射的3D骨组织支架。

Changsheng Lu, Runqing Shen, Xiao Wang
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引用次数: 0

摘要

目前研究的二维细胞培养系统通常不适合大规模细胞扩增,并且容易导致细胞形态改变、异常分化和蛋白质表达扭曲。为了克服这些限制,通过微流体制造技术开发了一种用于三维(3D)骨组织工程的甲基丙烯酸甘油酯改性丝素(SFMA)/甲基丙烯酸酐改性明胶(GelMA)互穿聚合物网络水凝胶(SFMA-GelMA)。随着SFMA含量的增加,SFMA- gelma中的分子链发生结构转变,从无规线圈转变为β-片状和β-晶体,存储模量提高到500 Pa左右,降解时间从47.7%提高到84.3%。在SFMA-GelMA中,具有精氨酸-甘氨酸-天冬氨酸序列的GelMA含量较高,有利于细胞早期粘附,提供直径为5-80 μm的互联孔,促进3D培养mc3t3 - e1成骨前细胞的成骨分化,碱性磷酸酶活性可达约45 U/mg蛋白。总之,SFMA-GelMA作为一种3D细胞培养支架和再生医学的可注射材料显示出巨大的潜力,特别是在骨组织工程中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biocompatible hydrogel microspheres based on modified silk fibroin and gelatin for injectable 3D bone tissue scaffolds.

Currently investigated two-dimensional cell culture systems are typically inadequate for large-scale cell expansion and prone to causing altered cell morphology, aberrant differentiation, and distorted protein expression. To overcome these limitations, a glycidyl methacrylate-modified silk fibroin (SFMA)/methacrylic anhydride-modified gelatin (GelMA) interpenetrating polymer network hydrogel (SFMA-GelMA) was developed via microfluidic fabrication for three-dimensional (3D) bone tissue engineering applications. With increased SFMA content, the molecular chains in SFMA-GelMA undergo a structural transformation from random coil toβ-sheet andβ-crystallite, enhancing storage modulus to about 500 Pa and extending degradation duration from about 47.7% to 84.3% mass retention over 7d. The higher GelMA content with the arginine-glycine-aspartic acid sequence in SFMA-GelMA facilitated early cell adhesion, provided interconnected pores (5-80 μm diameter), and promoted the osteogenic differentiation of MC3T3-E1preosteoblasts in 3D culture, as confirmed by alkaline phosphatase activity up to about 45 U mg-1protein. Overall, SFMA-GelMA shows substantial potential as a 3D cell culture scaffold and injectable material for regenerative medicine, particularly in bone tissue engineering.

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