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Macrophages are required for adult salamander limb regeneration.巨噬细胞是成体蝾螈肢体再生所必需的。
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The high-throughput highway to computational materials design.高通量高速公路通往计算材料设计。
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Adapting human pluripotent stem cells to high-throughput and high-content screening.将人类多能干细胞适应高通量和高内涵筛选。
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Novel methodology based on biomimetic superhydrophobic substrates to immobilize cells and proteins in hydrogel spheres for applications in bone regeneration.基于仿生超疏水基底的新型方法,用于将细胞和蛋白质固定在水凝胶球中,应用于骨再生。
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Combinatorial on-chip study of miniaturized 3D porous scaffolds using a patterned superhydrophobic platform.采用图案超疏水平台对小型化 3D 多孔支架进行组合式芯片研究。
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Acute inflammation initiates the regenerative response in the adult zebrafish brain.急性炎症会引发成年斑马鱼大脑的再生反应。
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Combinatorial discovery of polymers resistant to bacterial attachment.组合发现抗细菌附着的聚合物。
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8
Arrayed cellular microenvironments for identifying culture and differentiation conditions for stem, primary and rare cell populations.用于鉴定干细胞、原代细胞和稀有细胞群体的培养和分化条件的细胞微环境阵列。
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Combinatorial cell-3D biomaterials cytocompatibility screening for tissue engineering using bioinspired superhydrophobic substrates.采用仿生超疏水基底的组织工程细胞-3D 生物材料细胞相容性组合筛选
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Big data in small places.小地方里的大数据。
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体内对三维支架生物相容性的高内涵评估。

In vivo high-content evaluation of three-dimensional scaffolds biocompatibility.

作者信息

Oliveira Mariana B, Ribeiro Maximiano P, Miguel Sónia P, Neto Ana I, Coutinho Paula, Correia Ilídio J, Mano João F

机构信息

1 3B's Research Group-Biomaterials, Biodegradables and Biomimetics, University of Minho , Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, Taipas, Portugal .

出版信息

Tissue Eng Part C Methods. 2014 Nov;20(11):851-64. doi: 10.1089/ten.TEC.2013.0738. Epub 2014 Mar 31.

DOI:10.1089/ten.TEC.2013.0738
PMID:24568682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4229707/
Abstract

While developing tissue engineering strategies, inflammatory response caused by biomaterials is an unavoidable aspect to be taken into consideration, as it may be an early limiting step of tissue regeneration approaches. We demonstrate the application of flat and flexible films exhibiting patterned high-contrast wettability regions as implantable platforms for the high-content in vivo study of inflammatory response caused by biomaterials. Screening biomaterials by using high-throughput platforms is a powerful method to detect hit spots with promising properties and to exclude uninteresting conditions for targeted applications. High-content analysis of biomaterials has been mostly restricted to in vitro tests where crucial information is lost, as in vivo environment is highly complex. Conventional biomaterials implantation requires the use of high numbers of animals, leading to ethical questions and costly experimentation. Inflammatory response of biomaterials has also been highly neglected in high-throughput studies. We designed an array of 36 combinations of biomaterials based on an initial library of four polysaccharides. Biomaterials were dispensed onto biomimetic superhydrophobic platforms with wettable regions and processed as freeze-dried three-dimensional scaffolds with a high control of the array configuration. These chips were afterward implanted subcutaneously in Wistar rats. Lymphocyte recruitment and activated macrophages were studied on-chip, by performing immunocytochemistry in the miniaturized biomaterials after 24 h and 7 days of implantation. Histological cuts of the surrounding tissue of the implants were also analyzed. Localized and independent inflammatory responses were detected. The integration of these data with control data proved that these chips are robust platforms for the rapid screening of early-stage in vivo biomaterials' response.

摘要

在开发组织工程策略时,生物材料引起的炎症反应是一个不可避免且需要考虑的方面,因为它可能是组织再生方法的早期限制步骤。我们展示了具有图案化高对比度润湿性区域的扁平柔性薄膜作为可植入平台的应用,用于对生物材料引起的炎症反应进行高内涵体内研究。通过高通量平台筛选生物材料是一种强大的方法,可检测具有潜在特性的热点,并排除针对特定应用无趣的条件。生物材料的高内涵分析大多局限于体外测试,而在体外测试中会丢失关键信息,因为体内环境高度复杂。传统的生物材料植入需要使用大量动物,这引发了伦理问题且实验成本高昂。在高通量研究中,生物材料的炎症反应也一直被严重忽视。我们基于四种多糖的初始文库设计了一系列36种生物材料组合。将生物材料分配到具有可湿润区域的仿生超疏水平台上,并加工成具有高度阵列配置控制的冻干三维支架。这些芯片随后被皮下植入Wistar大鼠体内。通过在植入24小时和7天后对小型化生物材料进行免疫细胞化学,在芯片上研究淋巴细胞募集和活化巨噬细胞。还分析了植入物周围组织的组织学切片。检测到了局部且独立的炎症反应。将这些数据与对照数据整合证明,这些芯片是用于快速筛选体内生物材料早期反应的强大平台。