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Cited 80 time in webofscience Cited 91 time in scopus
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dc.contributor.authorSangho Lim-
dc.contributor.authorWon-Ju Kim-
dc.contributor.authorYeon-Ho Kim-
dc.contributor.authorSohee Lee-
dc.contributor.authorJa-Hyun Koo-
dc.contributor.authorJung-Ah Lee-
dc.contributor.authorHeeseok Yoon-
dc.contributor.authorDo-Hyun Kim-
dc.contributor.authorHong-Jai Park-
dc.contributor.authorKim, HM-
dc.contributor.authorHong-Gyun Lee-
dc.contributor.authorJi Yun Kim-
dc.contributor.authorJae-Ung Lee-
dc.contributor.authorJae Hun Shin-
dc.contributor.authorLark Kyun Kim-
dc.contributor.authorDoh, J-
dc.contributor.authorHye-Mi Kim-
dc.contributor.authorLee, SK-
dc.contributor.authorBothwell, ALM-
dc.contributor.authorSuh, M-
dc.contributor.authorChoi, JM-
dc.date.accessioned2016-01-08T14:51:31Z-
dc.date.available2016-01-08T14:51:31Z-
dc.date.created2015-10-09-
dc.date.issued2015-09-
dc.identifier.issn2041-1723-
dc.identifier.other2015-OAK-0000033602-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/13458-
dc.description.abstractCentral nervous system (CNS)-infiltrating effector T cells play critical roles in the development and progression of multiple sclerosis (MS). However, current drugs for MS are very limited due to the difficulty of delivering drugs into the CNS. Here we identify a cell-permeable peptide, dNP2, which efficiently delivers proteins into mouse and human T cells, as well as various tissues. Moreover, it enters the brain tissue and resident cells through blood vessels by penetrating the tightly organized blood-brain barrier. The dNP2-conjugated cytoplasmic domain of cytotoxic T-lymphocyte antigen 4 (dNP2-ctCTLA-4) negatively regulates activated T cells and shows inhibitory effects on experimental autoimmune encephalomyelitis in both preventive and therapeutic mouse models, resulting in the reduction of demyelination and CNS-infiltrating T helper 1 and T helper 17 cells. Thus, this study demonstrates that dNP2 is a blood-brain barrier-permeable peptide and dNP2-ctCTLA-4 could be an effective agent for treating CNS inflammatory diseases such as MS.-
dc.description.statementofresponsibilityopen-
dc.languageEnglish-
dc.publisherMacmillan Publishers Limited. All rights reserved-
dc.relation.isPartOfNATURE COMMUNICATIONS-
dc.subjectcytoplasmic domain of cytotoxic T lymphocyte antigen 4-
dc.subjectcytotoxic T lymphocyte antigen 4-
dc.subjectneuroprotective agent-
dc.subjectpeptide derivative-
dc.subjectrecombinant dNP2-
dc.subjectrecombinant protein-
dc.subjectunclassified drug-
dc.subjectblood-
dc.subjectcytology-
dc.subjectcytoplasm-
dc.subjectdrug-
dc.subjectexperimental study-
dc.subjectimmune response-
dc.subjectpeptide-
dc.subjectpermeability-
dc.subjectprotein-
dc.subjectrodent-
dc.subjectanimal cell-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectArticle-
dc.subjectblood brain barrier-
dc.subjectCD4+ T lymphocyte-
dc.subjectcell permeabilization-
dc.subjectcentral nervous system-
dc.subjectconfocal microscopy-
dc.subjectcontrolled study-
dc.subjectdemyelination-
dc.subjectdrug conjugation-
dc.subjectdrug penetration-
dc.subjectexperimental autoimmune encephalomyelitis-
dc.subjectfemale-
dc.subjectfluorescence microscopy-
dc.subjectHeLa cell line-
dc.subjecthuman-
dc.subjecthuman cell-
dc.subjectinflammatory disease-
dc.subjectmouse-
dc.subjectmouse model-
dc.subjectmultiple sclerosis-
dc.subjectneuroprotection-
dc.subjectnonhuman-
dc.subjectT lymphocyte-
dc.subjecttandem repeat-
dc.subjectTh1 cell-
dc.subjectTh17 cell-
dc.titledNP2 is a blood-brain barrier-permeable peptide enabling ctCTLA-4 protein delivery to ameliorate experimental autoimmune encephalomyelitis-
dc.typeArticle-
dc.contributor.college기계공학과-
dc.identifier.doi10.1038/NCOMMS9244-
dc.author.googleLim, S., Kim, W.-J., Kim, Y.-H., Lee, S., Koo, J.-H., Lee, J.-A., Yoon, H., Kim, D.-H., Park, H.-J., Kim, H.-M., Lee, H.-G., Yun Kim, J., Lee, J.-U., Hun Shin, J., Kyun Kim, L., Doh, J., Kim, H., Lee,-
dc.relation.volume6-
dc.relation.startpage8244-
dc.contributor.id10189091-
dc.relation.journalNATURE COMMUNICATIONS-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationNATURE COMMUNICATIONS, v.6, pp.8244-
dc.identifier.wosid000363017500015-
dc.date.tcdate2019-01-01-
dc.citation.startPage8244-
dc.citation.titleNATURE COMMUNICATIONS-
dc.citation.volume6-
dc.contributor.affiliatedAuthorDoh, J-
dc.identifier.scopusid2-s2.0-84941758039-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc24-
dc.description.scptc27*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusDISEASE-MODIFYING THERAPIES-
dc.subject.keywordPlusCELL-PENETRATING PEPTIDES-
dc.subject.keywordPlusVECTOR-MEDIATED STRATEGY-
dc.subject.keywordPlusMULTIPLE-SCLEROSIS-
dc.subject.keywordPlusTRANSDUCTION DOMAIN-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusCYTOPLASMIC DOMAIN-
dc.subject.keywordPlusHEPARAN-SULFATE-
dc.subject.keywordPlusFUSION PROTEINS-
dc.subject.keywordPlusINNATE IMMUNITY-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-

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