Literature DB >> 34089242

Imaging flow cytometry and fluorescence microscopy in assessing radiation response in lymphocytes from umbilical cord blood and cancer patients.

Matus Durdik1, Pavol Kosik1, Lukas Jakl1, Maria Kozackova1, Eva Markova1, Katarina Vigasova1, Katarina Beresova1, Jana Jakubikova2, Eva Horvathova3, Lucian Zastko1, Marta Fekete4, Ingrid Zavacka4, Margita Pobijakova4, Igor Belyaev1.   

Abstract

DNA double strand breaks (DSB) induced by ionizing radiation (IR) are usually measured using γH2AX/53BP1 DNA repair foci, that is considered to be the most sensitive assay for DSB analysis. While fluorescence microscopy (FM) is the gold standard for this analysis, imaging flow cytometry (IFC) may offer number of advantages such as lack of the fluorescence background, higher number of cells analyzed, and higher sensitivity in detection of DNA damage induced by IR at low doses. Along with appearance of γH2AX foci, the variable fraction of the cells exhibits homogeneously stained γH2AX signal resulting in so-called γH2AX pan-staining, which is believed to appear at early stages of apoptosis. Here, we investigated incidence of γH2AX pan-staining at different time points after irradiation with γ-rays using IFC and compared the obtained data with the data from FM. Appearance of γH2AX pan-staining during the apoptotic process was further analyzed by fluorescence-activated cell sorting (FACS) of cells at different stages of apoptosis and subsequent immunofluorescence analysis. Our results show that IFC was able to reveal dose dependence of pan-staining, while FM failed to detect all pan-staining cells. Moreover, we found that γH2AX pan-staining could be induced by therapeutic, but not low doses of γ-rays and correlate well with percentage of apoptotic cells was analyzed using flow cytometric Annexin-V/7-AAD assay. Further investigations showed that γH2AX pan-staining is formed in the early phases of apoptosis and remains until later stages of apoptotic process. Apoptotic DNA fragmentation as detected with comet assay using FM correlated with the percentage of live and late apoptotic/necrotic cells as analyzed by flow cytometry. Lastly, we successfully tested IFC for detection of γH2AX pan-staining and γH2AX/53BP1 DNA repair foci in lymphocyte of breast cancer patients after radiotherapy, which may be useful for assessing individual radiosensitivity in a clinically relevant cohort of patients.
© 2021 International Society for Advancement of Cytometry.

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Keywords:  53BP1; Metafer; apoptosis; breast cancer; human lymphocytes; imaging flow cytometry; ionizing radiation; radiotherapy; γH2AX foci and pan-staining

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Year:  2021        PMID: 34089242     DOI: 10.1002/cyto.a.24468

Source DB:  PubMed          Journal:  Cytometry A        ISSN: 1552-4922            Impact factor:   4.355


  1 in total

1.  The prognostic value of circulating lymphocyte counts and ABO blood group in lung cancer stereotactic body radiation therapy: a retrospective study.

Authors:  Meng Chen; Kuifei Chen; Shuling Li; Yinnan Meng; Yangyang Shi; Xiaofeng Chen; Haihua Yang
Journal:  J Thorac Dis       Date:  2022-02       Impact factor: 2.895

  1 in total

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