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Bone remodeling using a three-dimensional chitosan - hydroxyapatite scaffold seeded with hypoxic conditioned human amnion mesenchymal stem cells

机译:使用三维壳聚糖 - 羟基磷灰石支架播种骨质重塑,脱氧调节人胚芽间充质干细胞

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Background: Bone regeneration studies involving the use of chitosan–hydroxyapatite (Ch-HA) scaffold seeded with human amnion mesenchymal stem cells (hAMSCs) have largely incorporated tissue engineering experiments. However, at the time of writing, the results of such investigations remain unclear. Purpose: The aim of this study was to determine the osteogenic differentiation of the scaffold Ch-HA that is seeded with hAMSCs in the regeneration of calvaria bone defect. Methods: Ch-HA scaffold of 5 mm diameter and 2 mm height was created by lyophilisation and desalination method. hAMSCs were cultured in hypoxia environment (5% oxygen, 10% carbon dioxide, 15% nitrogen) and seeded on the scaffold. Twenty male Wistar rat subjects (8 – 10 weeks, 200 - 250 grams) were randomly divided into two groups: control and hydroxyapatite scaffold (HAS). Defects (similar size to scaffold size) were created in the calvaria bone of the all-group subjects, but a scaffold was subsequently implanted only in the treatment group members. Control group left without treatment. After observation lasting 1 and 8 weeks, the subjects were examined histologically and immunohistochemically. Statistical analysis was done using ANOVA test. Results: Angiogenesis; expression of vascular endothelial growth factor; bone morphogenetic protein; RunX-2; alkaline phosphatase; type-1 collagen; osteocalcin and the area of new trabecular bone were all significantly greater in the HAS group compared to the control group. Conclusion: The three-dimensional Ch-HA scaffold seeded with hypoxic hAMSCs induced bone remodeling in calvaria defect according to the expression of the osteogenic and angiogenic marker.
机译:背景:涉及使用壳聚糖 - 羟基磷灰石(CH-HA)支架的骨再生研究播种与人嗜源性间充质干细胞(HAMSCs)占有很大程度上掺入了组织工程实验。但是,在撰写本文时,此类调查的结果仍然不清楚。目的:本研究的目的是确定在Calvaria骨缺损的再生中播种的支架CH-HA的成骨分化。方法:通过冻干和脱盐法产生5mm直径和2mm高度的CH-HA支架。 HAMSCs在缺氧环境(5%氧气,10%二氧化碳,15%氮气)中培养并在支架上播种。二十只雄性Wistar大鼠受试者(8-10周,200 - 250克)随机分为两组:对照和羟基磷灰石支架(具有)。在全群受试者的Calvaria骨中产生缺陷(类似于支架尺寸),但随后仅在治疗组成员中植入支架。对照组没有治疗。观察持续1和8周后,受试者被组织学和免疫化化学检查。使用ANOVA测试完成统计分析。结果:血管生成;血管内皮生长因子的表达;骨形态发生蛋白; Runx-2;碱性磷酸酶; 1型胶原蛋白;与对照组相比,骨钙素和新的小梁骨的面积均明显更大。结论:根据骨质发生和血管生成标记的表达,缺氧HAMSCs诱导缺氧HAMSCs造成骨质重塑的三维CH-HA支架。

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