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Transient receptor potential melastatin 2 governs stress-induced depressive-like behaviors

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dc.contributor.authorKo, Seung Yeon-
dc.contributor.authorWang, Sung Eun-
dc.contributor.authorLee, Han Kyu-
dc.contributor.authorJo, Sungsin-
dc.contributor.authorHan, Jinil-
dc.contributor.authorLee, Seung Hoon-
dc.contributor.authorChoi, Miyeon-
dc.contributor.authorJo, Hye-Ryeong-
dc.contributor.authorSeo, Jee Young-
dc.contributor.authorJung, Sung Jun-
dc.contributor.authorSon, Hyeon-
dc.date.accessioned2022-07-10T14:57:30Z-
dc.date.available2022-07-10T14:57:30Z-
dc.date.created2021-05-12-
dc.date.issued2019-01-
dc.identifier.issn0027-8424-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/148559-
dc.description.abstractMajor depressive disorder (MDD) is a devastating disease that arises in a background of environmental risk factors, such as chronic stress, that produce reactive oxygen species (ROS) in the brain. The chronic stress-induced ROS production involves Ca2+ signals; however, the mechanism is poorly understood. Transient receptor potential melastatin type 2 (TRPM2) is a Ca2+-permeable cation channel that is highly expressed in the brain. Here we show that in animal models of chronic unpredictable stress (CUS), deletion of TRPM2 (Trpm2(-/-)) produces antidepressant-like behaviors in mice. This phenotype correlates with reduced ROS, ROS-induced calpain activation, and enhanced phosphorylation of two Cdk5 targets including synapsin 1 and histone deacetylase 5 that are linked to synaptic function and gene expression, respectively. Moreover, TRPM2 mRNA expression is increased in hippocampal tissue samples from patients with MDD. Our findings suggest that TRPM2 is a key agent in stress-induced depression and a possible target for treating depression.-
dc.language영어-
dc.language.isoen-
dc.publisherNATL ACAD SCIENCES-
dc.titleTransient receptor potential melastatin 2 governs stress-induced depressive-like behaviors-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, Sung Jun-
dc.contributor.affiliatedAuthorSon, Hyeon-
dc.identifier.doi10.1073/pnas.1814335116-
dc.identifier.scopusid2-s2.0-85060809900-
dc.identifier.wosid000456944600049-
dc.identifier.bibliographicCitationPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, v.116, no.5, pp.1770 - 1775-
dc.relation.isPartOfPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-
dc.citation.titlePROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-
dc.citation.volume116-
dc.citation.number5-
dc.citation.startPage1770-
dc.citation.endPage1775-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusHIPPOCAMPAL NEUROGENESIS-
dc.subject.keywordPlusPREFRONTAL CORTEX-
dc.subject.keywordPlusMAJOR DEPRESSION-
dc.subject.keywordPlusCELL-DEATH-
dc.subject.keywordPlusTRPM2-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusP35-
dc.subject.keywordPlusPATHOPHYSIOLOGY-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordAuthorTRPM2-
dc.subject.keywordAuthordepression-
dc.subject.keywordAuthorROS-
dc.subject.keywordAuthorCdk5-
dc.subject.keywordAuthorneurogenesis-
dc.identifier.urlhttps://www.pnas.org/content/116/5/1770-
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서울 의과대학 > 서울 생화학·분자생물학교실 > 1. Journal Articles
서울 의과대학 > 서울 생리학교실 > 1. Journal Articles

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COLLEGE OF MEDICINE (DEPARTMENT OF BIOCHEMISTRY & MOLECULAR BIOLOGY)
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