CAJ | 학술논문

背景:海藻酸有相对温和的凝胶条件与良好的生物相容性,已广泛应用于生物组织工程.目的:采用海藻酸钠凝胶复合异种骨的方法,构建骨组织工程载体,观察载体中细胞的生物性能及体内成骨能力.方法:取2只2周龄新西兰兔的骨髓,以1 ×10~(-8)mol/L重组人骨形态发生蛋白2诱导骨髓间充质干细胞.取诱导后第2代骨髓间充质干细胞接种于1%海藻酸钠凝胶中,培养4 d苏木精-伊红染色观察凝胶中细胞形态.将第2代骨髓间充质干细胞分为单纯DMEM凝胶组和含1%海藻酸钠的DMEM凝胶组,分别培养7 d后行骨形态发生蛋白2免疫组织化学染色观察.取24只裸鼠,随机分为2组,于两侧股部肌袋中分别植入骨髓间充质干细胞,海藻酸钠凝胶/牛松质骨复合体作为实验组,骨髓间充质干细胞,牛松质骨复合体作为对照组.术后2,4周后组织学观察复合体成骨情况,图像分析系统分析各组成骨或软骨的面积百分比.结果与结论:海藻酸钠凝胶中骨髓间充质干细胞形态饱满,细胞悬浮于凝胶中,可见细胞分裂和核分裂相.单纯DMEM凝胶组和含1%海藻酸钠的DMEM凝胶组免疫组织化学观察,细胞分裂增殖正常,伸出多种形态的突起,胞核大,核仁清晰.单纯DMEM凝胶组和含1%海藻酸钠的DMEM凝胶组的骨形态发生蛋白2表达阳性率差异无显著性意义(P>0.05).扫描电镜观察海藻酸钠凝胶均匀地复合于牛松质骨微孔中,不同平面均有细胞生长.动物实验显示术后2,4周实验组和对照组的成骨或软骨的面积百分比差异有显著性意义(P<0.05).提示以海藻酸钠凝胶,牛松质骨构建骨组织工程载体,合乎组织工程载体的超结构原理,能最大限度地承载细胞,生物性能好,对骨髓间充质干细胞增殖和成骨表型及相关的生物性能无不良影响,在体内成骨效率较高.
배경:해조산유상대온화적응효조건여량호적생물상용성,이엄범응용우생물조직공정.목적:채용해조산납응효복합이충골적방법,구건골조직공정재체,관찰재체중세포적생물성능급체내성골능력.방법:취2지2주령신서란토적골수,이1 ×10~(-8)mol/L중조인골형태발생단백2유도골수간충질간세포.취유도후제2대골수간충질간세포접충우1%해조산납응효중,배양4 d소목정-이홍염색관찰응효중세포형태.장제2대골수간충질간세포분위단순DMEM응효조화함1%해조산납적DMEM응효조,분별배양7 d후행골형태발생단백2면역조직화학염색관찰.취24지라서,수궤분위2조,우량측고부기대중분별식입골수간충질간세포,해조산납응효/우송질골복합체작위실험조,골수간충질간세포,우송질골복합체작위대조조.술후2,4주후조직학관찰복합체성골정황,도상분석계통분석각조성골혹연골적면적백분비.결과여결론:해조산납응효중골수간충질간세포형태포만,세포현부우응효중,가견세포분렬화핵분렬상.단순DMEM응효조화함1%해조산납적DMEM응효조면역조직화학관찰,세포분렬증식정상,신출다충형태적돌기,포핵대,핵인청석.단순DMEM응효조화함1%해조산납적DMEM응효조적골형태발생단백2표체양성솔차이무현저성의의(P>0.05).소묘전경관찰해조산납응효균균지복합우우송질골미공중,불동평면균유세포생장.동물실험현시술후2,4주실험조화대조조적성골혹연골적면적백분비차이유현저성의의(P<0.05).제시이해조산납응효,우송질골구건골조직공정재체,합호조직공정재체적초결구원리,능최대한도지승재세포,생물성능호,대골수간충질간세포증식화성골표형급상관적생물성능무불량영향,재체내성골효솔교고.
BACKGROUND: Alginic acid has a relatively mild gel condition and good biocompatibility, and it has been widely used in bio-tissue engineering.OBJECTIVE: To construct bone tissue engineering scaffolds using alginate gel composite bone xenograft approach, and to observe the cell biological properties and in vivo osteogenic potential in scaffolds.METHODS: The bone marrow was harvested from two 2-week-old New Zealand rabbits, 1 ×10~(-8)mol/L recombinant human bone morphogenetic protein-2 was used to induce bone marrow mesenchymal stem cells. The induced bone marrow mesenchymal stem cells at the second generation were incubated into 1% sodium alginate gel, after cultured for 4 days, the cell morphology in gel was observed by hematoxylin-eosin staining. Bone marrow mesenchymal stem cells at the second generation were divided into simple DMEM gel group and DMEM containing 1% sodium alginate gel group, followed by a culture of 7 days. Then bone morphogenic protein-2 immunohistochemical staining was performed. A total of 24 nude mice were randomly divided into two groups, both sides of the thigh muscle pockets were implanted with bone marrow-derived mesenchymal stem cells/alginate gel/bovine cancellous bone complex as an experimental group, with bone marrow-derived mesenchymal stem cells/bovine cancellous bone as a control group. At 2 and 4 weeks post-operation, the osteogenesis in the composite was observed by histological examination, the percentage area of new bone or cartilage was determined using image analysis system.RESULTS AND CONCLUSION: The bone marrow-derived mesenchymal stern cells in the sodium alginate gel exhibited a well-stacked morphology, they suspended in a gel, showing cell division and mitosis phase. In the simple DMEM gel group and DMEM gel containing 1% sodium alginate group, the immunohistochemical results showed that, cell division and proliferation were normal, with prominence at a variety of forms, large nucleus, and clear nucleolus. The bone morphogenetic protein-2 expression had no significant difference between the simple DMEM gel group and DMEM gel containing 1% sodium alginate group (P>0.05).Scanning electron microscopy revealed that, the alginate gel evenly composited in bovine cancellous bone micropores, cell grew at different planes. Animal experiments showed that there were significant differences regarding the percentage of new bone or cartilage area between the experimental group and control group at 2 and 4 weeks postoperation (P< 0.05). It is indicated that constructing bone tissue engineering scaffolds by using alginate gel/bovine cancellous bone, complies with the ultra-structural principle of tissue engineering scaffolds, can maximize the cell loads, achieve good bio-performance, without adverse affects on the proliferation, osteogenic phenotype and related biological properties of bone marrow-derived mesenchymal stem calls, the in vivo osteogenic efficiency was high.