Phototoxicity of the fluorescent membrane dyes PKH2 and PKH26 on the human hematopoietic KG1a progenitor cell line

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dc.contributor.authorOh, DJko
dc.contributor.authorLee, Gyun Minko
dc.contributor.authorFrancis, K.ko
dc.contributor.authorPalsson, BOko
dc.date.accessioned2013-03-03T06:13:17Z-
dc.date.available2013-03-03T06:13:17Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1999-08-
dc.identifier.citationCYTOMETRY, v.36, no.4, pp.312 - 318-
dc.identifier.issn0196-4763-
dc.identifier.urihttp://hdl.handle.net/10203/77581-
dc.description.abstractBackground: The phototoxic effects of the well-known fluorescent membrane dyes PKH2 and PKH26 have been unknown, although their use in cell tracking experiments has increased dramatically. To eliminate the phototoxicity-induced alteration in cell function and morphology, it is essential to examine the suspicious phototoxicity of these dyes. Methods: Chemical and phototoxic effects of PKH dyes on the human hematopoietic KG1a cell line were examined. To minimize phototoxicity in long-term cell tracking experiments lasting up to 18 h with a fluorescence microscope system, time- lapse monitoring with different time intervals and exposure times was introduced. Results: There were no significant effects of the two PKH dyes on cell viability and growth when using dye concentrations up to 5 μM. However, when stained cells were exposed to excitation light, cell viability decreased dramatically, showing the phototoxicity of the PKH dyes. More than 60% of cells stained with 5 μM PKH26 died after 5 min of continuous light exposure. The phototoxic effect was more extensive in cells stained with higher concentrations of the dyes. Conclusions: We present guidelines for the optimal use of these dyes by using a defined hardware configuration.-
dc.languageEnglish-
dc.publisherJohn Wiley and Sons Inc.-
dc.subjectLYMPHOBLASTIC LEUKEMIC-CELLS-
dc.subjectMARROW STROMAL CELLS-
dc.subjectHAMSTER-CHEEK POUCH-
dc.subjectIN-VITRO-
dc.subjectPLATELET-AGGREGATION-
dc.subjectGROWTH-PARAMETERS-
dc.subjectINVIVO TRACKING-
dc.subjectVIVO-
dc.subjectSURVIVAL-
dc.subjectADHESION-
dc.titlePhototoxicity of the fluorescent membrane dyes PKH2 and PKH26 on the human hematopoietic KG1a progenitor cell line-
dc.typeArticle-
dc.identifier.wosid000081578600005-
dc.identifier.scopusid2-s2.0-0344848624-
dc.type.rimsART-
dc.citation.volume36-
dc.citation.issue4-
dc.citation.beginningpage312-
dc.citation.endingpage318-
dc.citation.publicationnameCYTOMETRY-
dc.identifier.doi10.1002/(SICI)1097-0320(19990801)36:4<312::AID-CYTO5>3.0.CO;2-V-
dc.contributor.localauthorLee, Gyun Min-
dc.contributor.nonIdAuthorOh, DJ-
dc.contributor.nonIdAuthorFrancis, K.-
dc.contributor.nonIdAuthorPalsson, BO-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorphototoxicity-
dc.subject.keywordAuthorPKH2-
dc.subject.keywordAuthorPKH26-
dc.subject.keywordAuthorfluorescence microscopy-
dc.subject.keywordAuthorhuman hematopoietic cell line-
dc.subject.keywordAuthorKG1a-
dc.subject.keywordAuthorcell tracking-
dc.subject.keywordPlusLYMPHOBLASTIC LEUKEMIC-CELLS-
dc.subject.keywordPlusMARROW STROMAL CELLS-
dc.subject.keywordPlusHAMSTER-CHEEK POUCH-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusPLATELET-AGGREGATION-
dc.subject.keywordPlusGROWTH-PARAMETERS-
dc.subject.keywordPlusINVIVO TRACKING-
dc.subject.keywordPlusVIVO-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusADHESION-
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