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dc.contributor.authorRahman, Md. Ataur-
dc.contributor.authorKim, Hanna-
dc.contributor.authorLee, Kang Ho-
dc.contributor.authorYun, Hyung-Mun-
dc.contributor.authorHong, Jung-Hwa-
dc.contributor.authorKim, Youngjae-
dc.contributor.authorChoo, Hyunah-
dc.contributor.authorPark, Mikyoung-
dc.contributor.authorRhim, Hyewhon-
dc.date.accessioned2024-01-20T01:03:32Z-
dc.date.available2024-01-20T01:03:32Z-
dc.date.created2021-09-05-
dc.date.issued2017-07-
dc.identifier.issn1016-8478-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/122572-
dc.description.abstractThe 5-HT6R has been considered as an attractive therapeutic target in the brain due to its exclusive expression in the brain. However, the mechanistic linkage between 5-HT(6)Rs and brain functions remains poorly understood. Here, we examined the effects of 5-HT6R-mediated cell morphological changes using immunocytochemistry, Western blot, and live-cell imaging assays. Our results showed that the activation of 5-HT(6)Rs caused morphological changes and increased cell surface area in HEK293 cells expressing 5-HT(6)Rs. Treatment with 5-HT specifically increased RhoA-GTP activity without affecting other Rho family proteins, such as Rac1 and Cdc42. Furthermore, live-cell imaging in hippocampal neurons revealed that activation of 5-HT(6)Rs using a selective agonist, ST1936, increased the density and size of dendritic protrusions along with the activation of RhoA-GTP activity and that both effects were blocked by pretreatment with a selective 5-HT6R antagonist, SB258585. Taken together, our results show that 5-HT6R plays an important role in the regulation of cell morphology via a RhoA-dependent pathway in mammalian cell lines and primary neurons.-
dc.languageEnglish-
dc.publisherKOREAN SOC MOLECULAR & CELLULAR BIOLOGY-
dc.subjectPHYSICAL INTERACTION-
dc.subjectDENDRITIC SPINES-
dc.subject5-HT6 RECEPTORS-
dc.subjectSMALL GTPASES-
dc.subjectSEROTONIN-
dc.subjectPLASTICITY-
dc.subjectACTIVATION-
dc.subjectMECHANISM-
dc.subjectNEURONS-
dc.title5-Hydroxytryptamine 6 Receptor (5-HT6R)-Mediated Morphological Changes via RhoA-Dependent Pathways-
dc.typeArticle-
dc.identifier.doi10.14348/molcells.2017.0080-
dc.description.journalClass1-
dc.identifier.bibliographicCitationMOLECULES AND CELLS, v.40, no.7, pp.495 - 502-
dc.citation.titleMOLECULES AND CELLS-
dc.citation.volume40-
dc.citation.number7-
dc.citation.startPage495-
dc.citation.endPage502-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART002247587-
dc.identifier.wosid000412952400007-
dc.identifier.scopusid2-s2.0-85029482643-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-
dc.type.docTypeArticle-
dc.subject.keywordPlusPHYSICAL INTERACTION-
dc.subject.keywordPlusDENDRITIC SPINES-
dc.subject.keywordPlus5-HT6 RECEPTORS-
dc.subject.keywordPlusSMALL GTPASES-
dc.subject.keywordPlusSEROTONIN-
dc.subject.keywordPlusPLASTICITY-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusNEURONS-
dc.subject.keywordAuthor5-HT6R-
dc.subject.keywordAuthordendritic protrusions-
dc.subject.keywordAuthorlive-cell imaging-
dc.subject.keywordAuthormorphology-
dc.subject.keywordAuthorserotonin-
dc.subject.keywordAuthorRhoA-GTP-
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