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Cited 22 time in webofscience Cited 21 time in scopus
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dc.contributor.authorKwang Hoon Song-
dc.contributor.authorKeon Woo Kwon-
dc.contributor.authorJong-Cheol Choi-
dc.contributor.authorJaeHwang Jung-
dc.contributor.authorYongKeun Park-
dc.contributor.authorKahp-Yang Suh-
dc.contributor.authorDoh, J-
dc.date.accessioned2015-06-25T02:06:28Z-
dc.date.available2015-06-25T02:06:28Z-
dc.date.created2014-07-18-
dc.date.issued2014-06-
dc.identifier.issn1757-9694-
dc.identifier.other2015-OAK-0000030043en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/10409-
dc.description.abstractIntraluminal crawling is considered to be important for extravasation of leukocytes in blood vessels, but biochemical/biophysical cues guiding the crawling of leukocytes have not been clearly understood. Here we provide evidence that T cells sense the topography of luminal surfaces and the nuclei of endothelial cells (ECs) using lamellipodia and filopodia, respectively, to optimize path finding during intraluminal crawling. Well-aligned EC layers or replicas of EC layers, which exhibit topography similar to that of EC layers, were fabricated, and flow was applied either parallel or perpendicular to the orientation of EC alignment. T cells crawled along the valleys of the topographical landscapes of the EC layers, while avoiding nuclei of ECs regardless of flow direction. Pharmacological inhibitor treatments revealed that sensing of topography and nuclei of EC layers was mediated by lamellipodia and filopodia, respectively. Lamellipodia or filopodia-inhibited T cells crawled significantly longer distances for extravasation than did normal T cells, indicating that sensing biophysical cues are critical for optimizing routes for extravasation.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherRoyal Society of Chemistry-
dc.relation.isPartOfIntegrative biology-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleT cells sense biophysical cues using lamellipodia and filopodia to optimize intraluminal path finding-
dc.typeArticle-
dc.contributor.college기계공학과en_US
dc.identifier.doi10.1039/C4IB00021H-
dc.author.googleSong, KHen_US
dc.author.googleKwon, KWen_US
dc.author.googleDoh, Jen_US
dc.author.googleSuh, KYen_US
dc.author.googlePark, Yen_US
dc.author.googleJung, Jen_US
dc.author.googleChoi, JCen_US
dc.relation.volume6en_US
dc.relation.issue4en_US
dc.relation.startpage450en_US
dc.relation.lastpage459en_US
dc.contributor.id10189091en_US
dc.relation.journalIntegrative biologyen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationIntegrative biology, v.6, no.4, pp.450 - 459-
dc.identifier.wosid000333331800008-
dc.date.tcdate2019-01-01-
dc.citation.endPage459-
dc.citation.number4-
dc.citation.startPage450-
dc.citation.titleIntegrative biology-
dc.citation.volume6-
dc.contributor.affiliatedAuthorDoh, J-
dc.identifier.scopusid2-s2.0-84896908327-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc15-
dc.description.scptc13*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusENDOTHELIAL-CELLS-
dc.subject.keywordPlusTRANSCELLULAR DIAPEDESIS-
dc.subject.keywordPlusARP2/3 COMPLEX-
dc.subject.keywordPlusATOMIC-FORCE-
dc.subject.keywordPlusMIGRATION-
dc.subject.keywordPlusMICROSCOPY-
dc.subject.keywordPlusADHESION-
dc.subject.keywordPlusNEUTROPHILS-
dc.subject.keywordPlusDYNAMICS-
dc.subject.keywordPlusFLOW-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-

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