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• W3048272802 startingPage "773" @default.
• W3048272802 abstract "Abstract It has been over half a century since cellular senescence was first noted and characterized, and yet no consensus senescent marker has been reliably established. This challenge is compounded by the complexity and heterogenic phenotypes of senescent cells. This necessitates the use of multiple biomarkers to confidently characterise senescent cells. Despite cytochemical staining of senescence associated-beta-galactosidase being a single marker approach, as well as being time and labour-intensive, it remains the most popular detection method. We have developed an alternative flow cytometry-based method that simultaneously quantifies multiple senescence markers at a single-cell resolution. In this study, we applied this assay to the quantification of both replicative and induced senescent primary cells. Using this assay, we were able to quantify the activity level of SA β-galactosidase, the expression level of p16 INK4a and γH2AX in these cell populations. Our results show this flow cytometric approach to be sensitive, robust, and consistent in discriminating senescent cells in different cell senescence models. A strong positive correlation between these commonly- used senescence markers was demonstrated. The method described in this paper can easily be scaled up to accommodate high-throughput screening of senescent cells in applications such as therapeutic cell preparation, and in therapy-induced senescence following cancer treatment." @default.
• W3048272802 created "2020-08-13" @default.
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• W3048272802 date "2020-08-10" @default.
• W3048272802 modified "2023-09-26" @default.
• W3048272802 title "Multiparameter flow cytometric detection and quantification of senescent cells in vitro" @default.
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• W3048272802 doi "https://doi.org/10.1007/s10522-020-09893-9" @default.
• W3048272802 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7541365" @default.
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• W3048272802 hasPublicationYear "2020" @default.
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