首页> 外文期刊>Journal of biomaterials applications >Three-dimensional culture of mouse pancreatic islet on a liver-derived perfusion-decellularized bioscaffold for potential clinical application
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Three-dimensional culture of mouse pancreatic islet on a liver-derived perfusion-decellularized bioscaffold for potential clinical application

机译:小鼠胰岛的三维培养在肝源性灌注脱细胞生物支架上的潜在临床应用

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The cutting-edge technology of three-dimensional liver decellularized bioscaffold has a potential to provide a micro-environment that is suitable for the resident cells and even develop a new functional organ. Liver decellularized bioscaffold preserved the native extracellular matrix and three-dimensional architecture in support of the cell culture. The goal of this study was to discover if three-dimensional extracellular matrix derived from mouse liver could facilitate the growth and maintenance of physiological functions of mouse isolated islets. We generated a whole organ liver decellularized bioscaffold which could successfully preserve extracellular matrix proteins and the native vascular channels using 1% Triton X-100/0.1% ammonium protocol. To evaluate the potential of decellularized liver as a scaffold for islets transplantation, the liver decellularized bioscaffold was infused with mouse primary pancreatic islets which were obtained through Collagenase P digestion protocol. Its yield, morphology, and quality were estimated by microscopic analysis, dithizone staining, insulin immunofluorescence and glucose stimulation experiments. Comparing the three-dimensional culture in liver decellularized bioscaffold with the orthodoxy two-dimensional plate culture, hematoxylin-eosin staining, immunohistochemistry, and insulin gene expression were tested. Our results demonstrated that the liver decellularized bioscaffold could support cellular culture and maintenance of cell functions. In contrast with the conventional two-dimensional culture, three-dimensional culture system could give rise to an up-regulated insulin gene expression. These findings demonstrated that the liver bioscaffold by a perfusion-decellularized technique could serve as a platform to support the survival and function of the pancreatic islets in vitro. Meanwhile three-dimensional culture system had a superior role in contrast with the two-dimensional culture. This study advanced the field of regenerative medicine towards the development of a liver decellularized bioscaffold capable of forming a neo-organ and could be used as potential clinical application.
机译:三维肝脏脱细胞生物支架的前沿技术有潜力提供适合驻留细胞的微环境,甚至发展出新的功能器官。肝脱细胞生物支架保留了天然的细胞外基质和三维结构,以支持细胞培养。这项研究的目的是发现源自小鼠肝脏的三维细胞外基质是否可以促进小鼠离体胰岛的生长和维持其生理功能。我们生成了一个全器官肝脏脱细胞的生物支架,该支架可以成功地使用1%Triton X-100 / 0.1%铵协议保存细胞外基质蛋白和天然血管通道。为了评估脱细胞肝作为胰岛移植支架的潜力,将肝脱细胞生物支架注入通过胶原酶P消化方案获得的小鼠原代胰岛。通过显微镜分析,双硫zone染色,胰岛素免疫荧光和葡萄糖刺激实验评估了其产量,形态和质量。将肝细胞脱细胞生物支架中的三维培养与传统的二维平板培养进行比较,测试了苏木精-伊红染色,免疫组织化学和胰岛素基因表达。我们的结果表明,肝脏脱细胞的生物支架可以支持细胞培养和维持细胞功能。与常规的二维培养相反,三维培养系统可以引起胰岛素基因表达上调。这些发现表明,通过灌注脱细胞技术的肝脏生物支架可以作为支持胰岛体外存活和功能的平台。同时,与二维文化相比,三维文化体系具有优越的作用。这项研究使再生医学领域朝着能够形成新器官的肝脱细胞生物支架的发展方向发展,并有望被用作潜在的临床应用。

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