BROWSE

Related Scientist

chang,youngtae's photo.

chang,youngtae
복잡계자기조립연구단
more info

ITEM VIEW & DOWNLOAD

Validation of CDr15 as a new dye for detecting neutrophil extracellular trap

DC Field Value Language
dc.contributor.authorKim S.-J.-
dc.contributor.authorKim J.-
dc.contributor.authorKim B.-
dc.contributor.authorLee W.-W.-
dc.contributor.authorLiu X.-
dc.contributor.authorYoung-Tae Chang-
dc.contributor.authorPark J.-W.-
dc.date.accessioned2020-12-22T03:02:01Z-
dc.date.accessioned2020-12-22T03:02:01Z-
dc.date.available2020-12-22T03:02:01Z-
dc.date.available2020-12-22T03:02:01Z-
dc.date.created2020-06-29-
dc.date.issued2020-06-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/7844-
dc.description.abstract© 2020 Elsevier Inc. Neutrophil extracellular trap (NET) is one of the first-line defenses against microbes. Under certain circumstances, however, it also plays an aggravating factor in diverse inflammation-related diseases including cancers and vascular diseases. Our aim is to develop a new method to detect NET in cells and tissues using a DNA-specific fluorescence probe CDr15. CDr15 was characterized to be impermeable to the cell membranes and to emit a strong fluorescence in association with extracellular DNAs in NET. Due to these properties, CDr15 was successfully shown to quantify NETs in vitro and to be applicable for real-time monitoring NET formation in PMA-stimulated neutrophils. Even in formaldehyde-fixed tumor specimens, CDr15 could detect NETs spreading around cancer cells. Compared with DAPI and SYTOX DNA dyes, CDr15 showed a lower level of background fluorescence and a higher specificity in NET detection. Based on these results, we propose CDr15 as a novel marker of NET to be applicable in experimental and clinical studies-
dc.description.uri1-
dc.language영어-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectCDr15-
dc.subjectDNA dye-
dc.subjectFluorescence imaging-
dc.subjectNeutrophil extracellular trap-
dc.titleValidation of CDr15 as a new dye for detecting neutrophil extracellular trap-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000537622800009-
dc.identifier.scopusid2-s2.0-85084641810-
dc.identifier.rimsid72216-
dc.contributor.affiliatedAuthorYoung-Tae Chang-
dc.identifier.doi10.1016/j.bbrc.2020.04.153-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.527, no.3, pp.646 - 653-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume527-
dc.citation.number3-
dc.citation.startPage646-
dc.citation.endPage653-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusNETOSIS-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordPlusPROMOTE-
dc.subject.keywordPlusNETS-
dc.subject.keywordPlusDNA-
dc.subject.keywordAuthorNeutrophil extracellular trap-
dc.subject.keywordAuthorCDr15-
dc.subject.keywordAuthorDNA dye-
dc.subject.keywordAuthorFluorescence imaging-
Appears in Collections:
Center for Self-assembly and Complexity(복잡계 자기조립 연구단) > 1. Journal Papers (저널논문)
Files in This Item:
There are no files associated with this item.

qrcode

  • facebook

    twitter

  • Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse