Cargando…

Enhanced γ‐H2AX DNA damage foci detection using multimagnification and extended depth of field in imaging flow cytometry

Accurate and rapid methods for the detection of DNA damage foci in eukaryotic cells are central to DNA repair studies, which identify differences in DNA repair capacity in cell lines. Such assays have been important in delineating mechanisms of DNA repair in human cells. Previously we were the first...

Descripción completa

Detalles Bibliográficos
Autores principales: Parris, Christopher N., Adam Zahir, Sheba, Al‐Ali, Hussein, Bourton, Emma C., Plowman, Christina, Plowman, Piers N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744970/
https://www.ncbi.nlm.nih.gov/pubmed/26087127
http://dx.doi.org/10.1002/cyto.a.22697
_version_ 1782414556399665152
author Parris, Christopher N.
Adam Zahir, Sheba
Al‐Ali, Hussein
Bourton, Emma C.
Plowman, Christina
Plowman, Piers N.
author_facet Parris, Christopher N.
Adam Zahir, Sheba
Al‐Ali, Hussein
Bourton, Emma C.
Plowman, Christina
Plowman, Piers N.
author_sort Parris, Christopher N.
collection PubMed
description Accurate and rapid methods for the detection of DNA damage foci in eukaryotic cells are central to DNA repair studies, which identify differences in DNA repair capacity in cell lines. Such assays have been important in delineating mechanisms of DNA repair in human cells. Previously we were the first to demonstrate the use of imaging flow cytometry for the detection of γ‐H2AX foci in cells exposed to ionizing radiation causing the induction of DNA strand breaks. In this report we extend these studies and show an enhancement of foci quantitation and image resolution using next generation imaging flow cytometry with the Amnis Imagestream(X) Mark II. We demonstrate using cell lines derived from normal individuals, and DNA double strand break repair defective cells that the number of foci observed is significantly increased when using 60× as compared to 40× magnification. Also, foci numbers and resolution is further increased with the application of the focus stacking (Extended Depth of Field–EDF) capacity activated. This report represents the first such demonstration of multimagnification and EDF for the enhanced quantitation of DNA damage in cells and provides a level of resolution, which near matches in situ microscopy methods for the detection of γ‐H2AX foci. © 2015 The Authors. Published by Wiley Periodicals Inc. on behalf of ISAC.
format Online
Article
Text
id pubmed-4744970
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-47449702016-02-18 Enhanced γ‐H2AX DNA damage foci detection using multimagnification and extended depth of field in imaging flow cytometry Parris, Christopher N. Adam Zahir, Sheba Al‐Ali, Hussein Bourton, Emma C. Plowman, Christina Plowman, Piers N. Cytometry A Special Section: Clinical Cell Cycle Analysis Accurate and rapid methods for the detection of DNA damage foci in eukaryotic cells are central to DNA repair studies, which identify differences in DNA repair capacity in cell lines. Such assays have been important in delineating mechanisms of DNA repair in human cells. Previously we were the first to demonstrate the use of imaging flow cytometry for the detection of γ‐H2AX foci in cells exposed to ionizing radiation causing the induction of DNA strand breaks. In this report we extend these studies and show an enhancement of foci quantitation and image resolution using next generation imaging flow cytometry with the Amnis Imagestream(X) Mark II. We demonstrate using cell lines derived from normal individuals, and DNA double strand break repair defective cells that the number of foci observed is significantly increased when using 60× as compared to 40× magnification. Also, foci numbers and resolution is further increased with the application of the focus stacking (Extended Depth of Field–EDF) capacity activated. This report represents the first such demonstration of multimagnification and EDF for the enhanced quantitation of DNA damage in cells and provides a level of resolution, which near matches in situ microscopy methods for the detection of γ‐H2AX foci. © 2015 The Authors. Published by Wiley Periodicals Inc. on behalf of ISAC. John Wiley and Sons Inc. 2015-06-18 2015-08 /pmc/articles/PMC4744970/ /pubmed/26087127 http://dx.doi.org/10.1002/cyto.a.22697 Text en © 2015 The Authors. Published by Wiley Periodicals, Inc. on behalf of ISAC. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Special Section: Clinical Cell Cycle Analysis
Parris, Christopher N.
Adam Zahir, Sheba
Al‐Ali, Hussein
Bourton, Emma C.
Plowman, Christina
Plowman, Piers N.
Enhanced γ‐H2AX DNA damage foci detection using multimagnification and extended depth of field in imaging flow cytometry
title Enhanced γ‐H2AX DNA damage foci detection using multimagnification and extended depth of field in imaging flow cytometry
title_full Enhanced γ‐H2AX DNA damage foci detection using multimagnification and extended depth of field in imaging flow cytometry
title_fullStr Enhanced γ‐H2AX DNA damage foci detection using multimagnification and extended depth of field in imaging flow cytometry
title_full_unstemmed Enhanced γ‐H2AX DNA damage foci detection using multimagnification and extended depth of field in imaging flow cytometry
title_short Enhanced γ‐H2AX DNA damage foci detection using multimagnification and extended depth of field in imaging flow cytometry
title_sort enhanced γ‐h2ax dna damage foci detection using multimagnification and extended depth of field in imaging flow cytometry
topic Special Section: Clinical Cell Cycle Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744970/
https://www.ncbi.nlm.nih.gov/pubmed/26087127
http://dx.doi.org/10.1002/cyto.a.22697
work_keys_str_mv AT parrischristophern enhancedgh2axdnadamagefocidetectionusingmultimagnificationandextendeddepthoffieldinimagingflowcytometry
AT adamzahirsheba enhancedgh2axdnadamagefocidetectionusingmultimagnificationandextendeddepthoffieldinimagingflowcytometry
AT alalihussein enhancedgh2axdnadamagefocidetectionusingmultimagnificationandextendeddepthoffieldinimagingflowcytometry
AT bourtonemmac enhancedgh2axdnadamagefocidetectionusingmultimagnificationandextendeddepthoffieldinimagingflowcytometry
AT plowmanchristina enhancedgh2axdnadamagefocidetectionusingmultimagnificationandextendeddepthoffieldinimagingflowcytometry
AT plowmanpiersn enhancedgh2axdnadamagefocidetectionusingmultimagnificationandextendeddepthoffieldinimagingflowcytometry