FAM19A5/TAFA5, a novel neurokine, plays a crucial role in depressive-like and spatial memory-related behaviors in mice

FAM19A5/TAFA5 is a member of the family with sequence similarity 19 with unknown function in emotional and cognitive regulation. Here, we reported that FAM19A5 was highly expressed in the embryonic and postnatal mouse brain, especially in the hippocampus. Behaviorally, genetic deletion of Fam19a5 re...

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Veröffentlicht in:Molecular psychiatry 2021-06, Vol.26 (6), p.2363-2379
Hauptverfasser: Huang, Shiyang, Zheng, Can, Xie, Guoguang, Song, Zhanming, Wang, Pingzhang, Bai, Yun, Chen, Dixin, Zhang, Yan, Lv, Ping, Liang, Weiwei, She, Shaoping, Li, Qingqing, Liu, Zhongtian, Wang, Yun, Xing, Guo-Gang, Wang, Ying
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container_issue 6
container_start_page 2363
container_title Molecular psychiatry
container_volume 26
creator Huang, Shiyang
Zheng, Can
Xie, Guoguang
Song, Zhanming
Wang, Pingzhang
Bai, Yun
Chen, Dixin
Zhang, Yan
Lv, Ping
Liang, Weiwei
She, Shaoping
Li, Qingqing
Liu, Zhongtian
Wang, Yun
Xing, Guo-Gang
Wang, Ying
description FAM19A5/TAFA5 is a member of the family with sequence similarity 19 with unknown function in emotional and cognitive regulation. Here, we reported that FAM19A5 was highly expressed in the embryonic and postnatal mouse brain, especially in the hippocampus. Behaviorally, genetic deletion of Fam19a5 resulted in increased depressive-like behaviors and impaired hippocampus-dependent spatial memory. These behavioral alterations were associated with the decreased expression of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors and N-methyl-D-aspartic acid receptors, as well as significantly reduced glutamate release and neuronal activity in the hippocampus. Subsequently, these changes led to the decreased density of dendritic spines. In recent years, the roles of chronic stress participating in the development of depression have become increasingly clear, but the mechanism remains to be elucidated. We found that the levels of FAM19A5 in plasma and hippocampus of chronic stress-treated mice were significantly decreased whereas overexpression of human FAM19A5 selectively in the hippocampus could attenuate chronic stress-induced depressive-like behaviors. Taken together, our results revealed for the first time that FAM19A5 plays a key role in the regulation of depression and spatial cognition in the hippocampus. Furthermore, our study provided a new mechanism for chronic stress-induced depression, and also provided a potential biomarker for the diagnosis and a new strategy for the treatment of depression.
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Here, we reported that FAM19A5 was highly expressed in the embryonic and postnatal mouse brain, especially in the hippocampus. Behaviorally, genetic deletion of Fam19a5 resulted in increased depressive-like behaviors and impaired hippocampus-dependent spatial memory. These behavioral alterations were associated with the decreased expression of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors and N-methyl-D-aspartic acid receptors, as well as significantly reduced glutamate release and neuronal activity in the hippocampus. Subsequently, these changes led to the decreased density of dendritic spines. In recent years, the roles of chronic stress participating in the development of depression have become increasingly clear, but the mechanism remains to be elucidated. We found that the levels of FAM19A5 in plasma and hippocampus of chronic stress-treated mice were significantly decreased whereas overexpression of human FAM19A5 selectively in the hippocampus could attenuate chronic stress-induced depressive-like behaviors. Taken together, our results revealed for the first time that FAM19A5 plays a key role in the regulation of depression and spatial cognition in the hippocampus. Furthermore, our study provided a new mechanism for chronic stress-induced depression, and also provided a potential biomarker for the diagnosis and a new strategy for the treatment of depression.</description><identifier>ISSN: 1359-4184</identifier><identifier>EISSN: 1476-5578</identifier><identifier>DOI: 10.1038/s41380-020-0720-x</identifier><identifier>PMID: 32317715</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/1 ; 13/106 ; 13/109 ; 13/31 ; 13/44 ; 13/51 ; 14/19 ; 38 ; 38/22 ; 38/39 ; 42 ; 45 ; 45/91 ; 631/378 ; 64/60 ; 692/699/476/1414 ; Animal cognition ; Aspartic acid ; Behavior ; Behavioral Sciences ; Biological Psychology ; Cognitive ability ; Dendritic spines ; Depression, Mental ; Development and progression ; Embryos ; Gene expression ; Genetic aspects ; Glutamic acid receptors ; Health aspects ; Hippocampus ; Hippocampus (Brain) ; Immunology ; Laboratory animals ; Medicine ; Medicine &amp; Public Health ; Memory ; Mental depression ; Mental disorders ; N-Methyl-D-aspartic acid receptors ; Nervous system ; Neurosciences ; Neurotrophic functions ; Pharmacotherapy ; Physiological aspects ; Plasma ; Polyclonal antibodies ; Proteins ; Psychiatry ; Risk factors ; Science ; Spatial memory ; Stem cells ; Stress</subject><ispartof>Molecular psychiatry, 2021-06, Vol.26 (6), p.2363-2379</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2020</rights><rights>COPYRIGHT 2021 Nature Publishing Group</rights><rights>The Author(s), under exclusive licence to Springer Nature Limited 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c505t-68a226a4e168d771b618923543b34dbdd565b6159d897f362414ef11e892f6f53</citedby><cites>FETCH-LOGICAL-c505t-68a226a4e168d771b618923543b34dbdd565b6159d897f362414ef11e892f6f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32317715$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Shiyang</creatorcontrib><creatorcontrib>Zheng, Can</creatorcontrib><creatorcontrib>Xie, Guoguang</creatorcontrib><creatorcontrib>Song, Zhanming</creatorcontrib><creatorcontrib>Wang, Pingzhang</creatorcontrib><creatorcontrib>Bai, Yun</creatorcontrib><creatorcontrib>Chen, Dixin</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Lv, Ping</creatorcontrib><creatorcontrib>Liang, Weiwei</creatorcontrib><creatorcontrib>She, Shaoping</creatorcontrib><creatorcontrib>Li, Qingqing</creatorcontrib><creatorcontrib>Liu, Zhongtian</creatorcontrib><creatorcontrib>Wang, Yun</creatorcontrib><creatorcontrib>Xing, Guo-Gang</creatorcontrib><creatorcontrib>Wang, Ying</creatorcontrib><title>FAM19A5/TAFA5, a novel neurokine, plays a crucial role in depressive-like and spatial memory-related behaviors in mice</title><title>Molecular psychiatry</title><addtitle>Mol Psychiatry</addtitle><addtitle>Mol Psychiatry</addtitle><description>FAM19A5/TAFA5 is a member of the family with sequence similarity 19 with unknown function in emotional and cognitive regulation. 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We found that the levels of FAM19A5 in plasma and hippocampus of chronic stress-treated mice were significantly decreased whereas overexpression of human FAM19A5 selectively in the hippocampus could attenuate chronic stress-induced depressive-like behaviors. Taken together, our results revealed for the first time that FAM19A5 plays a key role in the regulation of depression and spatial cognition in the hippocampus. 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Here, we reported that FAM19A5 was highly expressed in the embryonic and postnatal mouse brain, especially in the hippocampus. Behaviorally, genetic deletion of Fam19a5 resulted in increased depressive-like behaviors and impaired hippocampus-dependent spatial memory. These behavioral alterations were associated with the decreased expression of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors and N-methyl-D-aspartic acid receptors, as well as significantly reduced glutamate release and neuronal activity in the hippocampus. Subsequently, these changes led to the decreased density of dendritic spines. In recent years, the roles of chronic stress participating in the development of depression have become increasingly clear, but the mechanism remains to be elucidated. We found that the levels of FAM19A5 in plasma and hippocampus of chronic stress-treated mice were significantly decreased whereas overexpression of human FAM19A5 selectively in the hippocampus could attenuate chronic stress-induced depressive-like behaviors. Taken together, our results revealed for the first time that FAM19A5 plays a key role in the regulation of depression and spatial cognition in the hippocampus. Furthermore, our study provided a new mechanism for chronic stress-induced depression, and also provided a potential biomarker for the diagnosis and a new strategy for the treatment of depression.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32317715</pmid><doi>10.1038/s41380-020-0720-x</doi><tpages>17</tpages></addata></record>
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13/31
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13/51
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38/22
38/39
42
45
45/91
631/378
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692/699/476/1414
Animal cognition
Aspartic acid
Behavior
Behavioral Sciences
Biological Psychology
Cognitive ability
Dendritic spines
Depression, Mental
Development and progression
Embryos
Gene expression
Genetic aspects
Glutamic acid receptors
Health aspects
Hippocampus
Hippocampus (Brain)
Immunology
Laboratory animals
Medicine
Medicine & Public Health
Memory
Mental depression
Mental disorders
N-Methyl-D-aspartic acid receptors
Nervous system
Neurosciences
Neurotrophic functions
Pharmacotherapy
Physiological aspects
Plasma
Polyclonal antibodies
Proteins
Psychiatry
Risk factors
Science
Spatial memory
Stem cells
Stress
title FAM19A5/TAFA5, a novel neurokine, plays a crucial role in depressive-like and spatial memory-related behaviors in mice
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