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 |
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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. |
doi_str_mv | 10.1038/s41380-020-0720-x |
format | Article |
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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 & 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. 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><subject>13/1</subject><subject>13/106</subject><subject>13/109</subject><subject>13/31</subject><subject>13/44</subject><subject>13/51</subject><subject>14/19</subject><subject>38</subject><subject>38/22</subject><subject>38/39</subject><subject>42</subject><subject>45</subject><subject>45/91</subject><subject>631/378</subject><subject>64/60</subject><subject>692/699/476/1414</subject><subject>Animal cognition</subject><subject>Aspartic acid</subject><subject>Behavior</subject><subject>Behavioral Sciences</subject><subject>Biological Psychology</subject><subject>Cognitive ability</subject><subject>Dendritic spines</subject><subject>Depression, Mental</subject><subject>Development and progression</subject><subject>Embryos</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Glutamic acid receptors</subject><subject>Health aspects</subject><subject>Hippocampus</subject><subject>Hippocampus (Brain)</subject><subject>Immunology</subject><subject>Laboratory animals</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Memory</subject><subject>Mental depression</subject><subject>Mental disorders</subject><subject>N-Methyl-D-aspartic acid receptors</subject><subject>Nervous system</subject><subject>Neurosciences</subject><subject>Neurotrophic functions</subject><subject>Pharmacotherapy</subject><subject>Physiological aspects</subject><subject>Plasma</subject><subject>Polyclonal antibodies</subject><subject>Proteins</subject><subject>Psychiatry</subject><subject>Risk factors</subject><subject>Science</subject><subject>Spatial memory</subject><subject>Stem 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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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-68a226a4e168d771b618923543b34dbdd565b6159d897f362414ef11e892f6f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>13/1</topic><topic>13/106</topic><topic>13/109</topic><topic>13/31</topic><topic>13/44</topic><topic>13/51</topic><topic>14/19</topic><topic>38</topic><topic>38/22</topic><topic>38/39</topic><topic>42</topic><topic>45</topic><topic>45/91</topic><topic>631/378</topic><topic>64/60</topic><topic>692/699/476/1414</topic><topic>Animal cognition</topic><topic>Aspartic acid</topic><topic>Behavior</topic><topic>Behavioral Sciences</topic><topic>Biological Psychology</topic><topic>Cognitive ability</topic><topic>Dendritic spines</topic><topic>Depression, Mental</topic><topic>Development and progression</topic><topic>Embryos</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Glutamic acid receptors</topic><topic>Health aspects</topic><topic>Hippocampus</topic><topic>Hippocampus (Brain)</topic><topic>Immunology</topic><topic>Laboratory animals</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Memory</topic><topic>Mental depression</topic><topic>Mental disorders</topic><topic>N-Methyl-D-aspartic acid receptors</topic><topic>Nervous system</topic><topic>Neurosciences</topic><topic>Neurotrophic functions</topic><topic>Pharmacotherapy</topic><topic>Physiological aspects</topic><topic>Plasma</topic><topic>Polyclonal antibodies</topic><topic>Proteins</topic><topic>Psychiatry</topic><topic>Risk factors</topic><topic>Science</topic><topic>Spatial memory</topic><topic>Stem cells</topic><topic>Stress</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences 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psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Shiyang</au><au>Zheng, Can</au><au>Xie, Guoguang</au><au>Song, Zhanming</au><au>Wang, Pingzhang</au><au>Bai, Yun</au><au>Chen, Dixin</au><au>Zhang, Yan</au><au>Lv, Ping</au><au>Liang, Weiwei</au><au>She, Shaoping</au><au>Li, Qingqing</au><au>Liu, Zhongtian</au><au>Wang, Yun</au><au>Xing, Guo-Gang</au><au>Wang, Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FAM19A5/TAFA5, a novel neurokine, plays a crucial role in depressive-like and spatial memory-related behaviors in mice</atitle><jtitle>Molecular psychiatry</jtitle><stitle>Mol Psychiatry</stitle><addtitle>Mol Psychiatry</addtitle><date>2021-06-01</date><risdate>2021</risdate><volume>26</volume><issue>6</issue><spage>2363</spage><epage>2379</epage><pages>2363-2379</pages><issn>1359-4184</issn><eissn>1476-5578</eissn><abstract>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.</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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subjects | 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 & 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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