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유전체항상성연구단
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Quantitative Analysis of Cell Proliferation by a Dye Dilution Assay: Application to Cell Lines and Cocultures

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dc.contributor.authorSoobin Chung-
dc.contributor.authorSeol-Hee Kim-
dc.contributor.authorYuri Seo-
dc.contributor.authorSook-Kyung Kim-
dc.contributor.authorJi Youn Lee-
dc.date.available2018-01-08T05:17:20Z-
dc.date.created2017-08-29-
dc.date.issued2017-07-
dc.identifier.issn1552-4922-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/4184-
dc.description.abstractCell proliferation represents one of the most fundamental processes in biological systems, thus the quantitative analysis of cell proliferation is important in many biological applications such as drug screening, production of biologics, and assessment of cytotoxicity. Conventional proliferation assays mainly quantify cell number based on a calibration curve of a homogeneous cell population, and therefore are not applicable for the analysis of cocultured cells. Moreover, these assays measure cell proliferation indirectly, based on cellular metabolic activity or DNA content. To overcome these shortcomings, a dye dilution assay employing fluorescent cell tracking dyes that are retained within cells was applied and was diluted proportionally by subsequent cell divisions. Here, it was demonstrated that this assay could be implemented to quantitatively analyze the cell proliferation of different types of cell lines, and to concurrently analyze the proliferation of two types of cell lines in coculture by utilizing cell tracking dyes with different spectral characteristics. The mean division time estimated by the dye dilution assay is compared with the population doubling time obtained from conventional methods and values from literature. Additionally, dye transfer between cocultured cells was investigated and it was found that it is a characteristic of the cells rather than a characteristic of the dye. It was suggested that this method can be easily combined with other flow cytometric analyses of cellular properties, providing valuable information on cell status under diverse conditions. (C) 2017 International Society for Advancement of Cytometry-
dc.description.uri1-
dc.language영어-
dc.publisherWILEY-BLACKWELL-
dc.subjectcell proliferation-
dc.subjectdye dilution-
dc.subjectCFSE-
dc.subjectcell lines-
dc.subjectcoculture-
dc.subjectcell division (doubling) time-
dc.subjectdye transfer-
dc.titleQuantitative Analysis of Cell Proliferation by a Dye Dilution Assay: Application to Cell Lines and Cocultures-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000405907100011-
dc.identifier.scopusid2-s2.0-85017353673-
dc.identifier.rimsid60000-
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorYuri Seo-
dc.identifier.doi10.1002/cyto.a.23105-
dc.identifier.bibliographicCitationCYTOMETRY PART A, v.91, no.7, pp.704 - 712-
dc.citation.titleCYTOMETRY PART A-
dc.citation.volume91-
dc.citation.number7-
dc.citation.startPage704-
dc.citation.endPage712-
dc.date.scptcdate2018-10-01-
dc.description.wostc1-
dc.description.scptc2-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusMEASURING LYMPHOCYTE-PROLIFERATION-
dc.subject.keywordPlusDIACETATE SUCCINIMIDYL ESTER-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusFLUORESCENT DYES-
dc.subject.keywordPlusTRACK PROLIFERATION-
dc.subject.keywordPlusFLOW-CYTOMETRY-
dc.subject.keywordPlusCFSE-
dc.subject.keywordPlusDIVISION-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusPOPULATION-
dc.subject.keywordAuthorcell proliferation-
dc.subject.keywordAuthordye dilution-
dc.subject.keywordAuthorCFSE-
dc.subject.keywordAuthorcell lines-
dc.subject.keywordAuthorcoculture-
dc.subject.keywordAuthorcell division (doubling) time-
dc.subject.keywordAuthordye transfer-
Appears in Collections:
Center for Genomic Integrity(유전체 항상성 연구단) > 1. Journal Papers (저널논문)
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