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作 者:倪云峰[1] 李小飞[1] 刘源[2] 雷战军[2] 卢强[1]
机构地区:[1]第四军医大学唐都医院胸外科 [2]第四军医大学口腔医学院病理学教研室,陕西西安710033
出 处:《第四军医大学学报》2006年第7期612-614,共3页Journal of the Fourth Military Medical University
基 金:国家自然科学基金(39970707);陕西省自然科学基金(99SM37)
摘 要:目的:探讨骨髓基质干细胞(MSCs)与软骨细胞混和培养体内成软骨的可行性.方法:分离、培养、扩传兔MSCs及软骨细胞,二者按一定比例混和(3∶1),以6.0×1010/L的细胞密度接种于PGA(聚羟基乙酸)支架作为共培养组,以相同密度的单纯MSCs和单纯软骨细胞分别接种以作为阴性与阳性对照.将细胞PGA材料复合物种植在成兔皮下,各标本于体内培养8wk时取材,通过大体观察、组织学等方法对新生软骨进行初步评价.结果:各组细胞与PGA支架的黏附良好.混和培养组及阳性对照组(软骨细胞组)体内培养8wk后均形成了成熟的软骨组织,并基本保持了复合物初始的大小和形状,两组新生软骨外观及组织学特征基本相同.阴性对照组(单纯MSCs组)在体内培养过程中未形成软骨组织,而是形成了纤维结缔组织.结论:软骨微环境在MSCs成软骨分化及体内软骨形成中具有重要作用,软骨细胞能有效地诱导MSCs向软骨细胞分化并促进MSCs体内软骨形成.AIM: To explore the feasibility of in vivo chondrogenesis by co-culture of mesenchymal stem cells (MSCs) and chondrocytes. METHODS: Rabbit MSCs and chondrocytes were in vitro isolated, cultured and expanded respectively and then were mixed at a ratio of 3 : 1 ( MSCs: chondrocytes). The mixed cells were seeded onto PGA scaffold at the ultimate concentration of 6.0 × 10^10/L as co-culture group. MSCs and chondrocytes of the same ultimate concentration were seeded respectively onto the scaffold as negative control group( MSCs group)and positive control group( chondrocyte group). Then, the cell-scaffold constructs were transplanted into subcutaneous tissue of adult rabbits. All specimens were harvested after in vivo culture for 8 weeks. Gross observation and histology were used to evaluate the new cartilage. RESULTS: Cells in all groups had a fine adhesion to the scaffold. In both co-culture group and positive control group, the cellscaffold constructs could maintain the original size and shape during in vivo culture and formed homogenous mature cartilage after 8 weeks of in vivo culture. Furthermore, the neo-cartilages in both groups were similar to each other in gross appearance and histological features. In negative control group, the cartilage was not formed but the connective tissue. CONCLUSION: Chondrocytes can provide a chondrogenic to induce a chondrogenic differentiation of MSCs and thus promote the chon-drogenesis of MSCs in vivo.
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