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dc.contributor.authorJeon, Hyungju-
dc.contributor.authorHojin Lee-
dc.contributor.authorKwon, Dae-Hyuk-
dc.contributor.authorKim, Jiwon-
dc.contributor.authorKeiko, Yamamoto-
dc.contributor.authorYook, Jang Soo-
dc.contributor.authorFENG, LINQING-
dc.contributor.authorPark, Hye Ran-
dc.contributor.authorLim, Yong Hoon-
dc.contributor.authorCho, Zang-Hee-
dc.contributor.authorPaek, Sun Ha-
dc.contributor.authorKim, Jinhyun-
dc.date.accessioned2024-01-19T12:31:50Z-
dc.date.available2024-01-19T12:31:50Z-
dc.date.created2022-04-05-
dc.date.issued2022-03-
dc.identifier.issn2211-1247-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/115551-
dc.description.abstractThe subthalamic nucleus (STN) controls psychomotor activity and is an efficient therapeutic deep brain stimulation target in individuals with Parkinson's disease. Despite evidence indicating position-dependent therapeutic effects and distinct functions within the STN, the input circuit and cellular profile in the STN remain largely unclear. Using neuroanatomical techniques, we construct a comprehensive connectivity map of the indirect and hyperdirect pathways in the mouse STN. Our circuit-and cellular-level connectivities reveal a topographically graded organization with three types of indirect and hyperdirect pathways (external globus pallidus only, STN only, and collateral). We confirm consistent pathways into the human STN by 7 T MRIbased tractography. We identify two functional types of topographically distinct glutamatergic STN neurons (parvalbumin [PV+/-]) with synaptic connectivity from indirect and hyperdirect pathways. Glutamatergic PV+ STN neurons contribute to burst firing. These data suggest a complex interplay of information integration within the basal ganglia underlying coordinated movement control and therapeutic effects.-
dc.languageEnglish-
dc.publisherCell Press-
dc.titleTopographic connectivity and cellular profiling reveal detailed input pathways and functionally distinct cell types in the subthalamic nucleus-
dc.typeArticle-
dc.identifier.doi10.1016/j.celrep.2022.110439-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCell Reports, v.38, no.9-
dc.citation.titleCell Reports-
dc.citation.volume38-
dc.citation.number9-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000764832100007-
dc.identifier.scopusid2-s2.0-85125234191-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalResearchAreaCell Biology-
dc.type.docTypeArticle-
dc.subject.keywordPlusDEEP BRAIN-STIMULATION-
dc.subject.keywordPlusTRIPARTITE SUBDIVISION HYPOTHESIS-
dc.subject.keywordPlusGLUTAMATE-RECEPTOR SUBUNITS-
dc.subject.keywordPlusBASAL GANGLIA-
dc.subject.keywordPlusGLOBUS-PALLIDUS-
dc.subject.keywordPlusENTOPEDUNCULAR NUCLEUS-
dc.subject.keywordPlusSYNAPTIC CONNECTIVITY-
dc.subject.keywordPlusPARKINSONS-DISEASE-
dc.subject.keywordPlusNEURONS-
dc.subject.keywordPlusRAT-
dc.subject.keywordAuthorindirect and hyperdirect pathways-
dc.subject.keywordAuthorsubthalamic nucleus-
dc.subject.keywordAuthorcell type-
dc.subject.keywordAuthorconnectivity-
dc.subject.keywordAuthorfiring pattern-
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