软骨修复使用Clematis 三萜皂苷输送微载体,在应用于兔模型前在微重力生物反应器中培养。
Cartilage Repair Using Clematis Triterpenoid Saponin Delivery Microcarrier, Cultured in a Microgravity Bioreactor Prior to Application in Rabbit Model.
机构信息
Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210029, P.R. China.
Laboratory of New Techniques of Restoration and Reconstruction of Orthopedics and Traumatology, Nanjing University of Chinese Medicine, Nanjing 210023, P.R. China.
出版信息
ACS Biomater Sci Eng. 2022 Feb 14;8(2):753-764. doi: 10.1021/acsbiomaterials.1c01101. Epub 2022 Jan 27.
Cartilage tissue engineering provides a promising method for the repair of articular cartilage defects, requiring appropriate biological scaffolds and necessary growth factors to enhance the efficiency of cartilage regeneration. Here, a silk fibroin (SF) microcarrier and a clematis triterpenoid saponin delivery SF (CTS-SF) microcarrier were prepared by the high-voltage electrostatic differentiation and lyophilization method, and chondrocytes were carried under the simulated microgravity condition by a rotating cell culture system. SF and CTS-SF microspheres were relatively uniform in size and had a porous structure with good swelling and cytocompatibility. Further, CTS-SF microcarriers could sustainably release CTSs in the monitored 10 days. Compared with the monolayer culture, chondrocytes under the microgravity condition maintained a better chondrogenic phenotype and showed better proliferation ability after culture on microcarriers. Moreover, the sustained release of CTS from CTS-SF microcarriers upregulated transforming growth factor-β, Smad2, and Smad3 signals, contributing to promote chondrogenesis. Hence, the biophysical effects of microgravity and bioactivities of CTS-ST were used for chondrocyte expansion and phenotype maintenance in vitro. With prolonged expansion, SF- and CTS-SF-based microcarrier-cell composites were directly implanted in vivo to repair rabbit articular defects. Gross evaluations, histopathological examinations, and biochemical analysis indicated that SF- and CTS-SF-based composites exhibited cartilage-like tissue repair compared with the nontreated group. Further, CTS-SF-based composites displayed superior hyaline cartilage-like repair that integrated with the surrounding cartilage better and higher cartilage extracellular matrix content. In conclusion, these results provide an alternative preparation method for drug-delivered SF microcarrier and a culture method for maintaining the chondrogenic phenotype of seed cells based on the microgravity environment. CTS showed its bioactive function, and the application of CTS-SF microcarriers can help repair and regenerate cartilage defects.
软骨组织工程为关节软骨缺损的修复提供了一种很有前途的方法,需要合适的生物支架和必要的生长因子来提高软骨再生的效率。在这里,通过高压静电分离和冷冻干燥法制备了丝素蛋白(SF)微载体和毛蕊花糖苷递送 SF(CTS-SF)微载体,并通过旋转细胞培养系统在模拟微重力条件下携带软骨细胞。SF 和 CTS-SF 微球大小相对均匀,具有多孔结构,具有良好的溶胀性和细胞相容性。此外,CTS-SF 微载体在监测的 10 天内可以持续释放 CTS。与单层培养相比,微重力条件下的软骨细胞在微载体上培养后保持更好的软骨形成表型,增殖能力更好。此外,CTS-SF 微载体中 CTS 的持续释放上调转化生长因子-β、Smad2 和 Smad3 信号,有助于促进软骨形成。因此,微重力的生物物理效应和 CTS-ST 的生物活性用于体外扩增和维持软骨细胞的表型。随着时间的延长,SF 和 CTS-SF 基微载体-细胞复合材料直接植入体内修复兔关节缺损。大体评估、组织病理学检查和生化分析表明,与未处理组相比,SF 和 CTS-SF 基复合材料表现出类似软骨的组织修复。进一步的,CTS-SF 基复合材料显示出优越的透明软骨样修复,与周围软骨更好地整合,并且软骨细胞外基质含量更高。总之,这些结果为基于微重力环境的药物递送 SF 微载体的制备方法和种子细胞软骨形成表型的维持提供了一种替代方法。CTS 显示出其生物活性功能,CTS-SF 微载体的应用有助于修复和再生软骨缺损。