Published August 31, 2022 | Version v1
Journal article Open

Spheroidal Model of SKBR3 and U87MG Cancer Cells for Live Imaging of Caspase-3 during Apoptosis Induced by Singlet Oxygen in Photodynamic Therapy

  • 1. Department of Biophysics, Institute of Physics, Faculty of Science, P.J. Safarik University in Kosice, Jesenna 5, 041 54 Kosice, Slovakia
  • 2. Institute of Animal Biochemistry and Genetics, Centre of Biosciences, Slovak Academy of Sciences, Dubravska cesta 9, 840 05 Bratislava, Slovakia
  • 3. Center for Interdisciplinary Biosciences, Technology and Innovation Park, P.J. Safarik University in Kosice, Jesenna 5, 041 54 Kosice, Slovakia

Contributors

Contact person:

  • 1. Center for Interdisciplinary Biosciences, Technology and Innovation Park, P.J. Safarik University in Kosice, Jesenna 5, 041 54 Kosice, Slovakia

Description

Aspects related to the response of cells to photodynamic therapy (PDT) have been well studied in cell cultures, which often grow in monolayers. In this work, we propose a spheroidal model of U87MG and SKBR3 cells designed to mimic superficial tumor tissue, small spheroids (<500 um) suitable for confocal fluorescence microscopy, and larger spheroids (>500 um) that can be xenografted
onto quail chorioallantoic membrane (CAM) to study the effects of PDT in real time. Hypericin was used as a model molecule for a hydrophobic photosensitizer that can produce singlet oxygen (1O2). 1O2 production by hypericin was detected in SKBR3 and U87MG spheroid models using a label-free technique. Vital fluorescence microscopy and flow cytometry revealed the heterogeneity of caspase-3 distribution in the cells of the spheroids. The levels of caspase-3 and apoptosis increased in the cells of spheroids 24 h after PDT. Lactate dehydrogenase activity was evaluated in the spheroids as the most reliable assay to detect differences in phototoxicity. Finally, we demonstrated the applicability of U87MG spheroids on CAM in photodiagnostics. Overall, the variability and applicability of the prepared spheroid models were demonstrated in the PDT study.

Notes

Ministry of education, science, research, and sport of the Slovak Republic, grant number VEGA 1/0557/20, VEGA 2/0042/21, Slovak Research and Development Agency through the project APVV-20-0340, APVV 20-0129, and by European Union's Horizon 2020 research. This publication is also the result of the project implementation: Open Scientific Community for Modern Interdisciplinary Research in Medicine (acronym: OPENMED), ITMS2014+: 313011V455, supported by the Operational Programme Integrated Infrastructure, funded by ERDF.

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Additional details

Funding

European Commission
CasProt – Fostering high scientific quality in protein research in Eastern Slovakia 952333