Uz Uzdan, Gunhan Kivanc, Vatansever Seda, Kivanc Mujde, Yuceturk Ali Vefa
University of Health Sciences, Izmir Bozyaka Training and Research Hospital, Department of Otorhinolaryngology-Head and Neck Surgery, Izmir.
Manisa Celal Bayar University, Department of Otorhinolaryngology-Head and Neck Surgery, Manisa.
J Craniofac Surg. 2019 May/Jun;30(3):940-943. doi: 10.1097/SCS.0000000000005374.
Cartilage created by tissue engineering is a promising new development in facial reconstructive surgery. The purpose of this study was to evaluate the histological results of implantation of synthetic polymer scaffold with chondrocytes differentiated from adipose-derived mesenchymal stem cells. Adipose tissue obtained from Wistar albino rats was dissociated, incubated and placed in culture medium. After a sufficient level of stem cell proliferation, the differentiation phase was started. Cells were collected on the 7th and 21st day of culture for chondrogenic characterization. After the 21st day of the differentiation phase of chondrocytes, they were transferred onto poly(dl-lactide-epsilon-caprolactone) synthetic polymer and culture continued for 24 hours. The scaffold with chondrocytes was then implanted into a subcutaneous area of skin on the back of the neck of the rat. Six weeks after implantation, all rats were sacrificed and the implantation areas were analyzed. Chondrocytes derived from adipogenic mesenchymal stem cells were stained positively with collagen II, aggrecan and Sox-9 after the differentiation stages. Histological examination of the excised material showed that chondrocytes were present, and the scaffold had been completely absorbed. The results of this study indicate that the differentiation method from mesenchymal stem cells to chondrogenic lineage was straightforward and scaffold with cells was easily accessible. This technique may be a good option for cartilage tissue engineering.
组织工程构建的软骨是面部重建手术中一项很有前景的新进展。本研究的目的是评估植入由脂肪来源的间充质干细胞分化而来的软骨细胞的合成聚合物支架的组织学结果。从Wistar白化大鼠获取脂肪组织,进行解离、孵育并置于培养基中。在干细胞增殖达到足够水平后,开始分化阶段。在培养的第7天和第21天收集细胞进行软骨生成特性分析。在软骨细胞分化阶段的第21天后,将它们转移到聚(dl-丙交酯-ε-己内酯)合成聚合物上并继续培养24小时。然后将带有软骨细胞的支架植入大鼠颈部背部皮肤的皮下区域。植入六周后,处死所有大鼠并分析植入区域。脂肪来源的间充质干细胞分化而来的软骨细胞在分化阶段后用II型胶原、聚集蛋白聚糖和Sox-9染色呈阳性。对切除材料的组织学检查表明存在软骨细胞,且支架已被完全吸收。本研究结果表明,从间充质干细胞向软骨生成谱系的分化方法简单直接,且带有细胞的支架易于获取。这项技术可能是软骨组织工程的一个不错选择。