摘要
目的采用超声振荡结合化学萃取法制备大鼠脱细胞脊髓支架，观察其三维结构及生物学特性，为脊髓组织工程研究提供理想的支架材料。方法采用超声振荡结合化学萃取（体积分数2％TritonX-100＋体积分数2％脱氧胆酸钠）方法对大鼠脊髓进行脱细胞处理（脱细胞脊髓组），对照正常大鼠脊髓组织（对照组），观察该脱细胞脊髓支架的大体形态、组织学及超微三维结构特点，并检测该支架材料的孔径大小、孔隙率、含水率、酶解率、在水溶液中稳定性等。结果脱细胞脊髓组原有的细胞成分被有效去除，具有（94．57±3．45）％的孔隙率和（88．62±1．0）％的含水率以及良好的三维空间结构（平均孔径为46μm），该支架在胰酶溶液中逐步降解，在第20小时达到（69．03±2．19）％，在双蒸水中逐步崩解，在第8天可达（62．55±1．70）％。正常脊髓组织结构紧密，含大量神经细胞及髓鞘，孔隙率和含水量分别为（0．04±0．02）％、（62．4±1．5）％，扫描电镜下未见明显孔隙结构，该支架在胰酶溶液中逐步降解，在第20小时达到（37．62±0．99）％，在双蒸水中逐步崩解，在第8天可达（40．97±0．81）％。结论超声振荡＋化学萃取所制备的脱细胞脊髓支架细胞成分去除彻底，细胞外基质成分保存完整，具有良好三维空间网状结构、良好的孔隙率和含水量，符合组织工程脊髓支架的理论要求，为组织工程脊髓支架提供理想的选择。
Objective To observe threedimensional structure and biological features of rat acellular spinal cord scaffold prepared by sonic oscillation and chemical extraction in order to offer an ideal scaffold for spinal cord tissue engineering research. Methods Rat spinal cord underwent acellular treatment with sonic oscillation and chemical extraction （Triton X100 at volume fracture of 2% and sodium deoxycholate at volume fracture of 2% ） （acellular spinal cord group）. In contrast with spinal cord tissue of normal rats （control group）, general morphology, histology and ultramicro threedimensional structure of acellular spinal cord scaffold were observed and aperture size, factor of porosity, water ratio, enzymolysis ratio and stability in water solution of the scaffold were also detected. Results Acellular spinal cord group showed effective removal of original cell components with factor of porosity for （94.57 ± 3.45） % and water content for （ 88.62±1.0） % , and satisfactory threedimensional structure with average aperture of 46 μm. Scaffold showed gradual degradation in enzymolysis solution and enzymolysis rate reached （69.03 ± 2.19）% at 20 hours. Besides, scaffold showed stepwise disintegration in double dis tilled water and hydrolysis rate was （ 62.55 ±1.70 ） % at 8 days. While, normal spinal cord showed close structure, generous neurons and myelin sheath with factor of porosity for （ 0.04 ± 0.02 ） % and water con tent for （62.4 ± 1. 5 ） %, and unobvious pore structure under scanning electron microscope. Normal spi nal cord were degraded gradually in enzymolysis solution and enzymolysis rate was （37.62 ± 0.9 ）% at 20hours. In the meantime, normal spinal cord were disintegrated gradually in double distilled water and hy drolysis rate was （40.97 ± 0.81 ）% at 8 days. Conclusions Aeellular spinal cord scaffold prepared by sonic oscillation plus chemical extraction achieves complete removal of cell components, intact ex tracellular matrix, and satisfactory results in thr
出处
《中华创伤杂志》
CAS
CSCD
北大核心
2013年第3期278-283,共6页
Chinese Journal of Trauma
基金
国家自然科学基金面上资助项目（81271362）
国家自然科学青年基金资助项目（31000438）
军队“十二五”重点课题资助项目（BWS11C040）
关键词
脊髓损伤
组织工程
超声处理
脱细胞脊髓支架
Spinal cord injuries
Tissue engineering
Sonication
Acellular spinalcord scaffold
