An inducible system for in vitro and in vivo Fas activation using FKBP-FRB-rapamycin complex
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Seokhwi Kim | - |
dc.contributor.author | Jongpil Shin | - |
dc.contributor.author | Hyunsik Oh | - |
dc.contributor.author | Sangphil Ahn | - |
dc.contributor.author | Nury, Kim | - |
dc.contributor.author | Won Do Heo | - |
dc.date.available | 2020-10-14T08:14:18Z | - |
dc.date.created | 2020-01-07 | - |
dc.date.issued | 2020-03 | - |
dc.identifier.issn | 0006-291X | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/7223 | - |
dc.description.abstract | © 2019 Elsevier Inc.The inducible activation system is valuable for investigating spatiotemporal roles of molecules. A chemically inducible activation system for Fas (CD95/APO-1), which works efficiently to induce apoptosis and leads non-apoptotic pathways, has not yet been developed. Here, we engineered a rapamycin-induced dimerization system of Fas consisting of FKBP and FRB proteins. Treatment of rapamycin specifically induces cellular apoptosis. In neurons and cells with high c-FLIP expression, rapamycin-induced Fas activation triggered the activation of the non-apoptotic pathway components instead of cell death. Intracranial delivery of the system could be utilized to induce apoptosis of tumor cells upon rapamycin treatment. Our results demonstrate a novel inducible Fas activation system which operates with high efficiency and temporal precision in vitro and in vivo promising a potential therapeutic strategy | - |
dc.language | 영어 | - |
dc.publisher | ACADEMIC PRESS INC ELSEVIER SCIENCE | - |
dc.title | An inducible system for in vitro and in vivo Fas activation using FKBP-FRB-rapamycin complex | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000524737600030 | - |
dc.identifier.scopusid | 2-s2.0-85076857268 | - |
dc.identifier.rimsid | 71028 | - |
dc.contributor.affiliatedAuthor | Nury, Kim | - |
dc.contributor.affiliatedAuthor | Won Do Heo | - |
dc.identifier.doi | 10.1016/j.bbrc.2019.12.072 | - |
dc.identifier.bibliographicCitation | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.523, no.2, pp.473 - 480 | - |
dc.relation.isPartOf | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
dc.citation.title | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
dc.citation.volume | 523 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 473 | - |
dc.citation.endPage | 480 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Biophysics | - |
dc.subject.keywordPlus | SPATIOTEMPORAL CONTROL | - |
dc.subject.keywordPlus | FACTOR RECEPTOR | - |
dc.subject.keywordPlus | BRAIN | - |
dc.subject.keywordPlus | CASPASE-8 | - |
dc.subject.keywordPlus | ABLATION | - |
dc.subject.keywordPlus | NEURONS | - |
dc.subject.keywordPlus | SIGNALS | - |
dc.subject.keywordPlus | SINGLE | - |
dc.subject.keywordPlus | GROWTH | - |
dc.subject.keywordPlus | ERK | - |
dc.subject.keywordAuthor | Fas | - |
dc.subject.keywordAuthor | Chemically inducible dimerization | - |
dc.subject.keywordAuthor | Rapamycin | - |
dc.subject.keywordAuthor | Apoptosis | - |
dc.subject.keywordAuthor | Non-apoptotic pathway | - |
dc.subject.keywordAuthor | Glioblastoma | - |