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多能前体细胞生成和分化微组织用于组织工程。

Generation and differentiation of microtissues from multipotent precursor cells for use in tissue engineering.

机构信息

Department of Oral and Maxillofacial Surgery, Heinrich Heine University Medical Center, Düsseldorf, Germany.

出版信息

Nat Protoc. 2011 Oct 13;6(11):1726-35. doi: 10.1038/nprot.2011.394.

Abstract

This protocol describes an effective method for the production of spherical microtissues (microspheres), which can be used for a variety of tissue-engineering purposes. The obtained microtissues are well suited for the study of osteogenesis in vitro when multipotent stem cells are used. The dimensions of the microspheres can easily be adjusted according to the cell numbers applied in an individual experiment. Thus, microspheres allow for the precise administration of defined cell numbers at well-defined sites. Here we describe a detailed workflow for the production of microspheres using unrestricted somatic stem cells from human umbilical cord blood and adapted protocols for the use of these microspheres in histological analysis. RNA extraction methods for mineralized microtissues are specifically modified for optimum yields. The duration of running the complete protocol without preparatory cell culture but including 2 weeks of microsphere incubation, histological staining and RNA isolation is about 3 weeks.

摘要

本方案描述了一种生产球形微组织(微球)的有效方法,该方法可用于多种组织工程目的。当使用多能干细胞时,获得的微组织非常适合体外成骨研究。微球的尺寸可以根据在单个实验中应用的细胞数量轻松调整。因此,微球允许在明确的部位精确施用明确数量的细胞。在此,我们描述了一种使用来自人脐带血的无限制体干细胞生产微球的详细工作流程,并为在组织学分析中使用这些微球制定了适应的方案。针对矿化微组织的 RNA 提取方法经过特别修改,以获得最佳产量。不包括预备细胞培养但包括 2 周微球孵育、组织学染色和 RNA 分离的完整方案运行时间约为 3 周。

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