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Enhancement of IGF-2-induced neurite outgrowth by IGF-binding protein-2 and osteoglycin in SH-SY5Y human neuroblastoma cells

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dc.contributor.authorJeong, Eun Young-
dc.contributor.authorKim, Sujoeng-
dc.contributor.authorJung, Soonwoong-
dc.contributor.authorKim, Gyeongwha-
dc.contributor.authorSon, Hyeonwi-
dc.contributor.authorLee, Dong Hoon-
dc.contributor.authorRoh, Gu Seob-
dc.contributor.authorKang, Sang Soo-
dc.contributor.authorCho, Gyeong Jae-
dc.contributor.authorChoi, Wan Sung-
dc.contributor.authorKim, Hyun Joon-
dc.date.accessioned2022-12-27T00:22:33Z-
dc.date.available2022-12-27T00:22:33Z-
dc.date.issued2013-08-
dc.identifier.issn0304-3940-
dc.identifier.issn1872-7972-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/20529-
dc.description.abstractA previous study using a mouse model of depression showed that chronic immobilization stress (CIS) reduces levels of insulin-like growth factor (IGF)-2, IGF binding protein 2 (IGFBP2), osteoglycin, and fibromodulin in the amygdala. Here, using human neuroblastoma cells, we tested whether these four proteins cooperatively modulate neuronal plasticity. We found that IGF-2 and IGFBP2 synergistically increased neurite outgrowth via enhanced early signaling through the IGF type 1 receptor. Furthermore, we found that osteoglycin, a small leucine-rich proteoglycan, significantly increased IGF-2/IGFPB2-induced neurite outgrowth, but fibromodulin had no effect. We also found that central amygdala neurons of CIS-induced depressive mouse showed a decreased total dendritic length. These findings suggest that CIS-responsive proteins modulate neuronal morphology during chronic stress. (C) 2013 Elsevier Ireland Ltd. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleEnhancement of IGF-2-induced neurite outgrowth by IGF-binding protein-2 and osteoglycin in SH-SY5Y human neuroblastoma cells-
dc.typeArticle-
dc.publisher.location아일랜드-
dc.identifier.doi10.1016/j.neulet.2013.05.038-
dc.identifier.scopusid2-s2.0-84880177912-
dc.identifier.wosid000322092000047-
dc.identifier.bibliographicCitationNeuroscience Letters, v.548, pp 249 - 254-
dc.citation.titleNeuroscience Letters-
dc.citation.volume548-
dc.citation.startPage249-
dc.citation.endPage254-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusGROWTH-FACTOR-BINDING-
dc.subject.keywordPlusLEUCINE-RICH PROTEOGLYCANS-
dc.subject.keywordPlusEXTRACELLULAR-MATRIX-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusFACTOR-II-
dc.subject.keywordPlusINSULIN-
dc.subject.keywordPlusNEURONS-
dc.subject.keywordAuthorIGF-2-
dc.subject.keywordAuthorIGFBP2-
dc.subject.keywordAuthorOsteoglycin-
dc.subject.keywordAuthorNeurite outgrowth-
dc.subject.keywordAuthorSH-SY5Y-
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