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Synthetic matrix containing glucocorticoid and growth factor for chondrogenic differentiation of stem cells

机译:含糖皮质激素和生长因子的合成基质用于干细胞软骨分化

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With the present study the aim was to assess the efficacy of synthetic matrix as specific drug carriers carrying encapsulation of cells for the differentiation using mesenchymal stem cells (MSCs). The poly(N-isopropylacrylamide-co-vinylimidazole); p(NiPAAm-co-VI)) matrix itself, synthetic matrix, without drugs was used as the control in order to determine the effects of these materials on differentiation. MSCs obtained from rabbit bone marrow were tested as a potential cell source for tissue regeneration encapsulated in synthetic matrix, in the presence or absence of the growth factor (TGF-β1) and dexamethasone (Dex). The encapsulated with cells and synthetic matrix were transplanted into a nude mouse as an injected form and cultured for up to 8 weeks. The specific gene expression was determined by RT-PCR analysis. The amount of cartilage-associated ECM proteins was examined by Safranin-O staining. These data indicate the potential use of TGF-β1 and Dex for reconstruction of neocartilage formation. We have concluded that synthetic matrix including TGF-β1 and Dex has useful carrier as containing inducers of chondrogenic differentiation materials in the regeneration of tissue-engineered cartilage in vivo.
机译:本研究的目的是评估合成基质作为特异药物载体的功效,该载体携带细胞包囊用于使用间充质干细胞(MSC)进行分化。聚(N-异丙基丙烯酰胺-共乙烯基咪唑);使用p(NiPAAm-co-VI)基质本身,无药物的合成基质作为对照,以确定这些材料对分化的影响。在存在或不存在生长因子(TGF-β1)和地塞米松(Dex)的情况下,将从兔骨髓获得的MSCs作为封装在合成基质中的组织再生的潜在细胞来源进行测试。用细胞和合成基质封装的胶囊以注射形式移植到裸鼠中,并培养长达8周。通过RT-PCR分析确定特异性基因表达。通过Safranin-O染色检查与软骨相关的ECM蛋白的量。这些数据表明TGF-β1和Dex可用于重建新软骨形成。我们已经得出结论,包括TGF-β1和Dex在内的合成基质在体内组织工程软骨的再生中具有作为软骨形成分化物质诱导剂的有用载体。

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