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Dynamic analysis of apoptosis using cyanine SYTO probes: from classical to microfluidic cytometry

journal contribution
posted on 2024-11-01, 13:37 authored by Donald WlodkowicDonald Wlodkowic, Joanna Skommer, Shannon Faley, Z Darzynkiewicz, J Cooper
Cell death is a stochastic process, often initiated and/or executed in a multi-pathway/multi-organelle fashion. Therefore, high-throughput single-cell analysis platforms are required to provide detailed characterization of kinetics and mechanisms of cell death in heterogeneous cell populations. However, there is still a largely unmet need for inert fluorescent probes, suitable for prolonged kinetic studies. Here, we compare the use of innovative adaptation of unsymmetrical SYTO dyes for dynamic real-time analysis of apoptosis in conventional as well as microfluidic chip-based systems. We show that cyanine SYTO probes allow non-invasive tracking of intracellular events over extended time. Easy handling and "stain-no wash" protocols open up new opportunities for high-throughput analysis and live-cell sorting. Furthermore, SYTO probes are easily adaptable for detection of cell death using automated microfluidic chip-based cytometry. Overall, the combined use of SYTO probes and state-of-the-art Lab-on-a-Chip platform emerges as a cost effective solution for automated drug screening compared to conventional Annexin V or TUNEL assays. In particular, it should allow for dynamic analysis of samples where low cell number has so far been an obstacle, e.g. primary cancer stems cells or circulating minimal residual tumors.

History

Related Materials

  1. 1.
    DOI - Is published in 10.1016/j.yexcr.2009.03.006
  2. 2.
    ISSN - Is published in 00144827

Journal

Experimental Cell Research

Volume

315

Issue

10

Start page

1706

End page

1714

Total pages

9

Publisher

Academic Press

Place published

United States

Language

English

Copyright

© 2009 Elsevier Inc. All rights reserved.

Former Identifier

2006040000

Esploro creation date

2020-06-22

Fedora creation date

2015-01-18

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