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Microstructuring of multiwell plates for three-dimensional cell culture applications by ultrasonic embossing

机译:通过超声压花对用于三维细胞培养的多孔板进行微结构化

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摘要

Since three-dimensional (3D) cell culture models better reflect tissues in vivo in terms of cell shape and microenvironment compared to conventional monolayer cultures, 3D tissue culture substrates gain more importance for a wide range of biological applications like drug discovery, toxicological studies, cancer and stem cell research. In this study we developed a method for the fabrication of 3D cell culture substrates in a multiwell plate format by microstructuring the bottom of 96-well cell culture plates using an ultrasonic embossing process. The resulting microstructured area consists of cubic micro-cavities in which adherent multicellular aggregates can be formed. We performed the biological evaluation of the system with the liver-derived human cell-line HepG2 and compared the novel substrate with a commercially available 3D culture system comprising porous alginate sponges. Metabolic activity (alamarBlue~® reduction) and induction of four biotransformation enzymes (EROD, ECOD, UGT, SULT) were determined by fluorimetry or HPLC. Our results revealed that HepG2 cells in microstructured plates showed a higher mitochondrial activity, as well as enzyme activity of ECOD and UGT after treatment with an inducer when compared to cells cultured in alginate sponges at otherwise comparable conditions. Since we have modified standard cell culture plates, the obtained system is adaptable to automated screening and might be useful for all kinds of cultures including adult, progenitor and stem cells which need a 3D culture configuration to restore or maintain the differentiated status.
机译:由于与常规单层培养相比,三维(3D)细胞培养模型在细胞形状和微环境方面能更好地反映体内组织,因此3D组织培养底物在诸如药物发现,毒理学研究,癌症等广泛的生物学应用中越来越重要和干细胞研究。在这项研究中,我们开发了一种通过使用超声波压花工艺微结构化96孔细胞培养板底部的多孔板形式制造3D细胞培养底物的方法。最终的微结构区域由立方微腔组成,可在其中形成粘附的多细胞聚集体。我们用肝脏来源的人类细胞系HepG2对系统进行了生物学评估,并将新型底物与包含多孔藻酸盐海绵的商业3D培养系统进行了比较。通过荧光测定法或HPLC测定代谢活性(减少)和四种生物转化酶(EROD,ECOD,UGT,SULT)的诱导。我们的结果表明,与在其他类似条件下在藻酸盐海绵中培养的细胞相比,用诱导剂处理后,微结构板中的HepG2细胞显示出更高的线粒体活性以及ECOD和UGT的酶活性。由于我们已经对标准细胞培养板进行了改良,因此所获得的系统适用于自动筛选,并且可能对包括3D培养结构以恢复或维持分化状态的成年,祖细胞和干细胞在内的各种培养均有用。

著录项

  • 来源
    《Biomedical Microdevices》 |2012年第2期|p.291-301|共11页
  • 作者单位

    Institute for Biological Interfaces, Karlsruhe Institute of Technology (Campus North), P.O. Box 3640, 76021 Karlsruhe, Germany,Department of Prosthodontics, Albert-Ludwigs-University, Hugstetter StraBe 55, 79106 Freiburg, Germany;

    Institute for Microstructure Technology, Karlsruhe Institute of Technology (Campus North), P.O. Box 3640, 76021 Karlsruhe, Germany;

    Institute for Biological Interfaces, Karlsruhe Institute of Technology (Campus North), P.O. Box 3640, 76021 Karlsruhe, Germany;

    Institute for Microstructure Technology, Karlsruhe Institute of Technology (Campus North), P.O. Box 3640, 76021 Karlsruhe, Germany;

    Institute for Microstructure Technology, Karlsruhe Institute of Technology (Campus North), P.O. Box 3640, 76021 Karlsruhe, Germany;

    Institute of Micro- and Nanotechnologies, IMN MacroNano~®, Ilmenau University of Technology, Gustav-Kirchhoff-Str. 5, 98693 Ilmenau, Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    3D cell culture; cell-based assays; high- throughput screenings; hepatocytes; biotransformation; ultrasonic embossing;

    机译:3D细胞培养;基于细胞的分析;高通量筛选;肝细胞生物转化超声波压花;

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