Duan Wei, Da Hu, Wang Wentao, Lü Shangjun, Xiong Zhuo, Liu Jian
Department of Orthopaedics, Shaanxi Provincial Corps Hospital, Chinese People's Armed Police Forces, Xi'an Shaanxi, 710054, P.R.China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2013 May;27(5):513-9.
To investigate the feasibility of fabricating an oriented scaffold combined with chondrogenic-induced bone marrow mesenchymal stem cells (BMSCs) for enhancement of the biomechanical property of tissue engineered cartilage in vivo.
Temperature gradient-guided thermal-induced phase separation was used to fabricate an oriented cartilage extracellular matrix-derived scaffold composed of microtubules arranged in parallel in vertical section. No-oriented scaffold was fabricated by simple freeze-drying. Mechanical property of oriented and non-oriented scaffold was determined by measurement of compressive modulus. Oriented and non-oriented scaffolds were seeded with chondrogenic-induced BMSCs, which were obtained from the New Zealand white rabbits. Proliferation, morphological characteristics, and the distribution of the cells on the scaffolds were analyzed by MTT assay and scanning electron microscope. Then cell-scaffold composites were implanted subcutaneously in the dorsa of nude mice. At 2 and 4 weeks after implantation, the samples were harvested for evaluating biochemical, histological, and biomechanical properties.
The compressive modulus of oriented scaffold was significantly higher than that of non-oriented scaffold (t=201.099, P=0.000). The cell proliferation on the oriented scaffold was significantly higher than that on the non-oriented scaffold from 3 to 9 days (P < 0.05). At 4 weeks, collagen type II immunohistochemical staining, safranin O staining, and toluidine blue staining showed positive results in all samples, but negative for collagen type I. There were numerous parallel giant bundles of densely packed collagen fibers with chondrocyte-like cells on the oriented-structure constructs. Total DNA, glycosaminoglycan (GAG), and collagen contents increased with time, and no significant difference was found between 2 groups (P > 0.05). The compressive modulus of the oriented tissue engineered cartilage was significantly higher than that of the non-oriented tissue engineered cartilage at 2 and 4 weeks after implantation (P < 0.05). Total DNA, GAG, collagen contents, and compressive modulus in the 2 tissue engineered cartilages were significantly lower than those in normal cartilage (P < 0.05).
Oriented extracellular matrix-derived scaffold can enhance the biomechanical property of tissue engineered cartilage and thus it represents a promising approach to cartilage tissue engineering.
研究构建定向支架结合软骨诱导骨髓间充质干细胞(BMSCs)以增强体内组织工程软骨生物力学性能的可行性。
采用温度梯度引导热诱导相分离法构建一种定向软骨细胞外基质衍生支架,其在垂直切片中由平行排列的微管组成。通过简单冷冻干燥制备无定向支架。通过测量压缩模量来确定定向和无定向支架的力学性能。将软骨诱导的BMSCs接种到定向和无定向支架上,这些细胞取自新西兰白兔。通过MTT法和扫描电子显微镜分析细胞的增殖、形态特征以及细胞在支架上的分布。然后将细胞 - 支架复合物皮下植入裸鼠背部。植入后2周和4周,采集样本以评估生化、组织学和生物力学性能。
定向支架的压缩模量显著高于无定向支架(t = 201.099,P = 0.000)。在第3至9天,定向支架上的细胞增殖显著高于无定向支架(P < 0.05)。在第4周,所有样本的II型胶原免疫组化染色、番红O染色和甲苯胺蓝染色均呈阳性结果,但I型胶原为阴性。在定向结构构建体上有许多平行的巨大束状紧密排列的胶原纤维以及类软骨细胞。总DNA、糖胺聚糖(GAG)和胶原含量随时间增加,两组之间无显著差异(P > 0.05)。植入后2周和4周,定向组织工程软骨的压缩模量显著高于无定向组织工程软骨(P < 0.05)。两种组织工程软骨中的总DNA、GAG、胶原含量和压缩模量均显著低于正常软骨(P < 0.05)。
定向细胞外基质衍生支架可增强组织工程软骨的生物力学性能,因此它是软骨组织工程的一种有前景的方法。