Nondestructive nanostraw intracellular sampling for longitudinal cell monitoring

  • Yuhong Cao
    Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305;
  • Martin Hjort
    Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305;
  • Haodong Chen
    Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA 94305;
  • Fikri Birey
    Department of Psychiatry and Behavioral Sciences, Stanford University Medical School, Stanford, CA 94305;
  • Sergio A. Leal-Ortiz
    Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305;
  • Crystal M. Han
    Department of Mechanical Engineering, Stanford University, Stanford, CA 94305
  • Juan G. Santiago
    Department of Mechanical Engineering, Stanford University, Stanford, CA 94305
  • Sergiu P. Paşca
    Department of Psychiatry and Behavioral Sciences, Stanford University Medical School, Stanford, CA 94305;
  • Joseph C. Wu
    Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA 94305;
  • Nicholas A. Melosh
    Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305;

書誌事項

公開日
2017-02-21
権利情報
  • http://www.pnas.org/site/misc/userlicense.xhtml
DOI
  • 10.1073/pnas.1615375114
公開者
Proceedings of the National Academy of Sciences

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説明

<jats:title>Significance</jats:title> <jats:p>Cell content analysis has rapidly become one of the most important new tools for measuring cell phenotype and behavior. However, the central limitation of current sampling technologies is they are destructive and must lyse the cells to measure the contents. This destruction prevents knowledge of prior or future states of the cell, which is particularly important for dynamic cell processes, such as development and differentiation. Here, we show a nondestructive longitudinal sampling and analysis platform that can sample repeatedly and accurately from the same single cell or group of cells over a long time period. We demonstrate sampling of both proteins and mRNA for cell lines as well as human-derived cardiomyocytes and astrocytes.</jats:p>

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