Mechanical property characterization of hundreds of single nuclei based on microfluidic constriction channel

Chun Chieh Chang, Ke Wang, Yi Zhang, Deyong Chen, Beiyuan Fan, Chia Hsun Hsieh, Junbo Wang*, Min Hsien Wu, Jian Chen

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

2 Scopus citations

Abstract

As label-free biomarkers, the mechanical properties of nuclei are widely treated as promising biomechanical markers for cell type classification and cellular status evaluation. However, previously reported mechanical parameters were derived from only around 10 nuclei, lacking statistical significances due to low sample numbers. To address this issue, nuclei were first isolated from SW620 and A549 cells, respectively, using a chemical treatment method. This was followed by aspirating them through two types of microfluidic constriction channels for mechanical property characterization. In this study, hundreds of nuclei were characterized, producing passage times of 0.5 ± 1.2 s for SW620 nuclei in type I constriction channel (n = 153), 0.045 ± 0.047 s for SW620 nuclei in type II constriction channel (n = 215) and 0.50 ± 0.86 s for A549 nuclei in type II constriction channel. In addition, neural network based pattern recognition was used to classify the nuclei isolated from SW620 and A549 cells, producing successful classification rates of 87.2% for diameters of nuclei, 85.5% for passage times of nuclei and 89.3% for both passage times and diameters of nuclei. These results indicate that the characterization of the mechanical properties of nuclei may contribute to the classification of different tumor cells.

Original languageEnglish
Pages (from-to)822-828
Number of pages7
JournalCytometry Part A
Volume93
Issue number8
DOIs
StatePublished - 08 2018

Bibliographical note

Publisher Copyright:
© 2018 International Society for Advancement of Cytometry

Keywords

  • constriction channel
  • mechanical properties
  • microfluidics
  • nucleus isolation
  • single-nucleus analysis

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