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Spraying Respiratory Epithelial Cells to Coat Tissue-Engineered Constructs

机译:喷涂呼吸道上皮细胞到外套组织工程的构造。

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摘要

Applying cells in a spray can overcome current hurdles in coating tissue engineered constructs with a thin layer of endo- or epithelial cells. We report here a structured study on the influences of spray application with a medical spray device on vascular smooth muscle cells (vSMCs) and respiratory epithelial cells (RECs) with and without fibrin gel. Next to viability and cytotoxicity assays, the in vitro differentiation capacity after spray processing was analyzed. For vSMC, no influence of air pressures till 0.8 bar could be shown, whereas the viability decreased for higher pressures. The viability of RECs was reduced to 88.5% with 0.4 bar air pressure. Lactate dehydrogenase-levels in the culture medium increased the first day after spraying but normalized afterward. In the short term, no differences by means of morphology and expression-specific markers for vSMCs and RECs were seen between the control and study group. In addition, in a long-term study for 28 days with the air–liquid interface, RECs differentiated and built up an organized epithelial layer with ciliary development that was comparable to the control for cells sprayed without fibrin gel. When spraying within fibrin gel, ciliary development was lower at 28 days. Thus, spraying of vSMCs and RECs was proved to be a suitable method for tissue engineering. Especially for RECs, this application is of special significance when coating luminal structures or other unfavorable topographies.
机译:在喷雾中施用细胞可以克服用薄层的内皮细胞或上皮细胞包被组织工程构建体的当前障碍。我们在这里报告了关于使用医用喷雾器喷雾对有或没有纤维蛋白凝胶的血管平滑肌细胞(vSMCs)和呼吸道上皮细胞(RECs)的影响的结构化研究。除了生存力和细胞毒性测定,还分析了喷雾处理后的体外分化能力。对于vSMC,直到0.8 bar才显示出气压的影响,而对于更高的压力,活力降低了。在0.4 bar气压下,RECs的活力降低至88.5%。喷雾后第一天培养基中的乳酸脱氢酶水平增加,但随后恢复正常。在短期内,对照组和研究组之间在形态学和表达特异性标记方面对vSMC和RECs没有差异。此外,在一项为期28天的气液界面长期研究中,RECs分化并建立了一个具有睫状发育的有组织的上皮层,与未注射纤维蛋白凝胶的细胞的对照相当。当在纤维蛋白凝胶内喷洒时,在28天时,睫状体发育降低。因此,事实证明,喷洒vSMC和RECs是组织工程的合适方法。特别是对于REC,当涂覆腔体结构或其他不利的地形时,此应用特别重要。

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