Synaptotagmin-4 induces anhedonic responses to chronic stress via BDNF signaling in the medial prefrontal cortex
DC Field | Value | Language |
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dc.contributor.author | Kim, Jeongseop | - |
dc.contributor.author | Seol, Sihwan | - |
dc.contributor.author | Kim, Tae-Eun | - |
dc.contributor.author | Lee, Joonhee | - |
dc.contributor.author | Koo, Ja Wook | - |
dc.contributor.author | Kang, Hyo Jung | - |
dc.date.accessioned | 2024-03-12T03:03:06Z | - |
dc.date.available | 2024-03-12T03:03:06Z | - |
dc.date.issued | 2024-02 | - |
dc.identifier.issn | 1226-3613 | - |
dc.identifier.issn | 2092-6413 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/72774 | - |
dc.description.abstract | Stressful circumstances are significant contributors to mental illnesses such as major depressive disorder. Anhedonia, defined as loss of the ability to enjoy pleasure in pleasurable situations, including rewarding activities or social contexts, is considered a key symptom of depression. Although stress-induced depression is associated with anhedonia in humans and animals, the underlying molecular mechanisms of anhedonic responses remain poorly understood. In this study, we demonstrated that synaptotagmin-4 (SYT4), which is involved in the release of neurotransmitters and neurotrophic factors, is implicated in chronic stress-induced anhedonia. Employing chronic unpredictable stress (CUS), we evaluated two subpopulations of mice, susceptible (SUS, anhedonic) and resilient (RES, nonanhedonic), based on sucrose preference, which was strongly correlated with social reward. The FosTRAP (targeted recombination in active populations) system and optogenetic approach revealed that neural activity in the medial prefrontal cortex (mPFC) was significantly associated with CUS-induced anhedonic behavioral phenotypes. By conducting weighted gene coexpression network analysis of RNA sequencing data from the mPFC of SUS and RES mice, we identified Syt4 as a hub gene in a gene network that was unique to anhedonia. We also confirmed that Syt4 overexpression in the mPFC was pro-susceptible, while Syt4 knockdown was pro-resilient; the pro-susceptible effects of SYT4 were mediated through a reduction in brain-derived neurotrophic factor (BDNF)-tropomyosin receptor kinase B (TrkB) signaling in the mPFC. These findings suggest that SYT4-BDNF interactions in the mPFC represent a crucial regulatory mechanism of anhedonic susceptibility to chronic stress. © 2024, The Author(s). | - |
dc.format.extent | 15 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Springer Nature | - |
dc.title | Synaptotagmin-4 induces anhedonic responses to chronic stress via BDNF signaling in the medial prefrontal cortex | - |
dc.type | Article | - |
dc.identifier.doi | 10.1038/s12276-024-01156-8 | - |
dc.identifier.bibliographicCitation | Experimental and Molecular Medicine, v.56, no.2, pp 329 - 343 | - |
dc.identifier.kciid | ART003057564 | - |
dc.description.isOpenAccess | Y | - |
dc.identifier.wosid | 001158303900009 | - |
dc.identifier.scopusid | 2-s2.0-85183740551 | - |
dc.citation.endPage | 343 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 329 | - |
dc.citation.title | Experimental and Molecular Medicine | - |
dc.citation.volume | 56 | - |
dc.type.docType | Article | - |
dc.publisher.location | 대한민국 | - |
dc.subject.keywordPlus | DEPRESSION-LIKE BEHAVIOR | - |
dc.subject.keywordPlus | GENOME-WIDE ASSOCIATION | - |
dc.subject.keywordPlus | ANXIETY-LIKE BEHAVIOR | - |
dc.subject.keywordPlus | NEUROTROPHIC FACTOR | - |
dc.subject.keywordPlus | TREATMENT RESISTANCE | - |
dc.subject.keywordPlus | SYNAPTIC FUNCTION | - |
dc.subject.keywordPlus | IV | - |
dc.subject.keywordPlus | DISORDER | - |
dc.subject.keywordPlus | RELEASE | - |
dc.subject.keywordPlus | RATS | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Research & Experimental Medicine | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Medicine, Research & Experimental | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
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