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作 者:黄跃[1] 沈国芳[2] 王旭东[2] 杨辛[3] 张秀丽[2] 蒋欣泉[2]
机构地区:[1]福建医科大学附属第一医院口腔颌面外科,福建福州350005 [2]上海交通大学医学院附属第九人民医院·口腔医学院口腔颌面外科,上海市口腔医学研究所,上海200011 [3]中山大学光华口腔医学院附属口腔医院,广东广州510055
出 处:《中国口腔颌面外科杂志》2009年第6期534-538,共5页China Journal of Oral and Maxillofacial Surgery
基 金:上海市科委启明星计划(04QMX1424)~~
摘 要:目的:比较用诱导因子诱导及用部分成体软骨细胞诱导的骨髓基质细胞(BMSCs)复合生物材料修复山羊颞下颌关节髁突软骨全层缺失的效果。方法:取山羊6只,分为2个实验组及1个对照组,每组2只。实验Ⅰ组植入经诱导因子(TGF-β1、IGF-1、地塞米松)诱导的BMSCs与支架(Pluronic F-127溶胶)复合物,实验Ⅱ组植入软骨细胞-BMSCs(按3∶7比例混合)的细胞-支架复合物,对照组仅植入支架材料。于术后8周取材,进行颞下颌关节软骨面缺失修复的大体观察、修复组织的HE染色、Ⅱ型胶原分泌的免疫组化染色。结果:术后8周实验Ⅱ组髁突软骨缺失区由软骨样组织修复。HE染色及免疫组化染色结果均提示修复组织为成熟的软骨组织。而实验Ⅰ组及材料对照组缺损区仅由少量的纤维性组织修复,不能形成成熟的软骨组织。结论:骨髓基质细胞在自体软骨细胞基质的诱导下,可以修复山羊髁突软骨面全层缺失,二维培养诱导后的BMSCs在山羊髁突软骨缺失区难以达到修复作用。PURPOSE: To repair the condylar cartilaginous defects by the differentiated bone marrow stromal cells (BMSCs) combined with Pluronic F-127. METHODS: 6 goats were randomly divided into 3 groups:2 experimental groups with 2 goats and the control group with 2 goats, respectively. In experimental group Ⅰ,BMSCs differentiated by TGF-β1,IGF-1 and dexamethasone were used.In experimental group Ⅱ,autologous BMSCs combined with chondrocytes were mixed with Pluronie F-127 and implanted into goat temporomandibular joint condylar cartilaginous defects.In control group,Pluronic F-127 gel was implanted into their condylar cartilaginous defects. The goats were sacrificed at 8-week. The reconstructive articular cartilage was evaluated by HE staining and immunostaining of type Ⅱ collagen. RESULTS: HE staining and immunostaining of type Ⅱ collagen showed that a layer of reconstructive articular cartilage in the experimental group Ⅱ, but there were no layer of reconstructive articular cartilage in the control group and experimental group Ⅰ. CONCLUSIONS: BMSCs induced by chondroeytes can be differentiated to ehondrocytes and used to repair the condylar articular cartilaginous defects in goats.
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