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Multiparameter cytometric analysis of complex cellular response
Š. Šimečková, R. Fedr, J. Remšík, Z. Kahounová, E. Slabáková, K. Souček,
Language English Country United States
Document type Journal Article
Grant support
NV15-33999A
MZ0
CEP Register
NV15-28628A
MZ0
CEP Register
Digital library NLK
Full text - Article
Full text - Article
Source
NLK
Free Medical Journals
from 2003 to 1 year ago
Medline Complete (EBSCOhost)
from 2012-06-01 to 1 year ago
Wiley Free Content
from 2003 to 1 year ago
PubMed
29220555
DOI
10.1002/cyto.a.23295
Knihovny.cz E-resources
- MeSH
- Apoptosis physiology MeSH
- Immunophenotyping methods MeSH
- Humans MeSH
- Cell Line, Tumor MeSH
- DNA Damage physiology MeSH
- Cell Proliferation physiology MeSH
- Flow Cytometry methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Complex analysis of cellular responses after experimental treatment is important for screening, mechanistic understanding of treatment effects, and the identification of sensitive and resistant cell phenotypes. Modern multicolor flow cytometry has demonstrated its power for such analyses. Here, we introduce a multiparametric protocol for complex analysis of cytokinetics by the simultaneous detection of seven fluorescence parameters. This analysis includes the detection of two surface markers for immunophenotyping, analysis of proliferation based on the cell cycle and the measurement of incorporated nucleoside analogue 5-ethynyl-2'-deoxyuridine (EdU) in newly synthesized DNA, analysis of DNA damage using an anti-phospho-histone H2A.X (Ser139) antibody, and determination of cell death using a fixable viability probe and intracellular detection of caspase-3 activation. To demonstrate the applicability of this protocol for the analysis of heterogeneous and complex cell responses, we used different treatments and model cell lines. We demonstrated that this protocol has the potential to provide complex and simultaneous analysis of cytokinetics and analyze the heterogeneity of the response at the single-cell level. © 2017 International Society for Advancement of Cytometry.
References provided by Crossref.org
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- $a Šimečková, Šárka $u Department of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic. Department of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech Republic.
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- $a Complex analysis of cellular responses after experimental treatment is important for screening, mechanistic understanding of treatment effects, and the identification of sensitive and resistant cell phenotypes. Modern multicolor flow cytometry has demonstrated its power for such analyses. Here, we introduce a multiparametric protocol for complex analysis of cytokinetics by the simultaneous detection of seven fluorescence parameters. This analysis includes the detection of two surface markers for immunophenotyping, analysis of proliferation based on the cell cycle and the measurement of incorporated nucleoside analogue 5-ethynyl-2'-deoxyuridine (EdU) in newly synthesized DNA, analysis of DNA damage using an anti-phospho-histone H2A.X (Ser139) antibody, and determination of cell death using a fixable viability probe and intracellular detection of caspase-3 activation. To demonstrate the applicability of this protocol for the analysis of heterogeneous and complex cell responses, we used different treatments and model cell lines. We demonstrated that this protocol has the potential to provide complex and simultaneous analysis of cytokinetics and analyze the heterogeneity of the response at the single-cell level. © 2017 International Society for Advancement of Cytometry.
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- $a Kahounová, Zuzana $u Department of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic. Center of Biomolecular and Cellular Engineering, International Clinical Research Center, St. Anne's University Hospital Brno, Brno, Czech Republic.
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