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首页> 外文期刊>Biomaterials >Co-cultivation of keratinocyte-human mesenchymal stem cell (hMSC) on sericin loaded electrospun nanofibrous composite scaffold (cationic gelatin/hyaluronan/chondroitin sulfate) stimulates epithelial differentiation in hMSCs: In vitro study
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Co-cultivation of keratinocyte-human mesenchymal stem cell (hMSC) on sericin loaded electrospun nanofibrous composite scaffold (cationic gelatin/hyaluronan/chondroitin sulfate) stimulates epithelial differentiation in hMSCs: In vitro study

机译:在装有丝胶的电纺纳米纤维复合支架(阳离子明胶/透明质酸/软骨素硫酸盐)上共培养角质形成细胞-人间充质干细胞(hMSC):刺激hMSCs的上皮分化:体外研究

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摘要

Fortifying the scaffold with bioactive molecules and glycosaminoglycans (GAGs), is an efficient way to design new generation tissue engineered biomaterials. In this study, we evaluated the synergistic effect of electrospun nanofibrous composite scaffold (cationic gelatin/hyaluronan/chondroitin sulfate) loaded with sericin and, contact co-culture of human mesenchymal stem cells (hMSCs)-keratinocytes on hMSCs' differentiation towards epithelial lineage. Cationic gelatin is prepared with one step novel synthesis process by grafting quaternary ammonium salts to the backbone of gelatin. Release kinetics studies showed that Fickian diffusion is the major release mechanism for both GAGs and sericin/gelatin. In vitro biocompatibility of the electrospun scaffold was evaluated in terms of LDH and DNA quantification assay on human foreskin fibroblast, human keratinocyte and hMSC. Significant proliferation (similar to 4-6 fold) was detected after culturing all three cell on the electrospun scaffold containing sericin. After 5 days of contact co-culture, results revealed that electrospun scaffold containing sericin promote epithelial differentiation of hMSC in terms of several protein markers (keratin 14, Delta Np63 alpha and Pan-cytokeratin) and gene expression of some dermal proteins (keratin 14, Delta Np63 alpha). Findings of this study will foster the progress of current skin tissue engineering scaffolds by understanding the skin regeneration and wound healing process. (C) 2016 Elsevier Ltd. All rights reserved.
机译:用生物活性分子和糖胺聚糖(GAG)加固支架,是设计新一代组织工程化生物材料的有效方法。在这项研究中,我们评估了装有丝胶的电纺纳米纤维复合支架(阳离子明胶/透明质酸/硫酸软骨素)的协同作用,以及人间充质干细胞(hMSCs)-角质形成细胞的接触共培养对hMSCs向上皮细胞系分化的影响。阳离子明胶是通过将季铵盐接枝到明胶主链上的一步合成方法制备的。释放动力学研究表明,菲克扩散是GAG和丝胶/明胶的主要释放机理。通过对人包皮成纤维细胞,人角质形成细胞和hMSC的LDH和DNA定量测定,评估了电纺支架的体外生物相容性。在含有丝胶的静电纺丝支架上培养所有三个细胞后,检测到显着增殖(类似于4-6倍)。接触共培养5天后,结果显示,含有丝胶的电纺丝支架可通过多种蛋白质标记(角蛋白14,Delta Np63α和泛细胞角蛋白)和某些皮肤蛋白质(角蛋白14)的基因表达促进hMSC的上皮分化。 Delta Np63 alpha)。这项研究的结果将通过了解皮肤再生和伤口愈合过程来促进当前皮肤组织工程支架的发展。 (C)2016 Elsevier Ltd.保留所有权利。

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