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Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis
Geranylgeranyltransferase I (GGT) is a prenyltransferase that mediates lipid modification of Rho small GTPases, such as Rho, Rac, and Cdc42, which are important for neuronal synaptogenesis. Although GGT is expressed in brain extensively, the function of GGT in central nerves system is largely unknow...
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Published in: | Journal of neurochemistry 2013-06, Vol.125 (5), p.698-712 |
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creator | Li, Zhengwei Sun, Chengdong Zhang, Tao Mo, Jianbing Shi, Qiong Zhang, Xianfeng Yuan, Maochun Chen, Long Mao, Xueqiang Yu, Rutong Zhou, Xiuping |
description | Geranylgeranyltransferase I (GGT) is a prenyltransferase that mediates lipid modification of Rho small GTPases, such as Rho, Rac, and Cdc42, which are important for neuronal synaptogenesis. Although GGT is expressed in brain extensively, the function of GGT in central nerves system is largely unknown so far. We have previously demonstrated that GGT promotes the basal and neuronal activity and brain‐derived neurotrophic factor (BDNF)‐induced dendritic morphogenesis of cultured hippocampal neurons and cerebellar slices. This study is to explore the function and mechanism of GGT in neuronal synaptogenesis. We found that the protein level and activity of GGT gradually increased in rat hippocampus from P7 to P28 and subcellular located at synapse of neurons. The linear density of Synapsin 1 and post‐synaptic density protein 95 increased by over‐expression of GGT β, while reduced by inhibition or down‐regulation of GGT. In addition, GGT and its known substrate Rac was activated by BDNF, which promotes synaptogenesis in cultured hippocampal neurons. Furthermore, BDNF‐induced synaptogenesis was eliminated by GGT inhibition or down‐regulation, as well as by non‐prenylated Rac1 over‐expression. Together, our data suggested that GGT mediates BDNF‐induced neuronal synaptogenesis through Rac1 activation.
Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis
Synaptogenesis is a complicated process of interaction between extracellular factors, such BDNF, and intracellular signaling, such as Rho family small GTPases. However, the mechanism that BDNF activated Rho family small GTPases and affected cytoskeletal reorganization and synapse formation remains unclear. In this sudy, we reported that GGT mediates BDNF‐induced neuronal synaptogenesis through small GTPase Rac1 activation. |
doi_str_mv | 10.1111/jnc.12249 |
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Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis
Synaptogenesis is a complicated process of interaction between extracellular factors, such BDNF, and intracellular signaling, such as Rho family small GTPases. However, the mechanism that BDNF activated Rho family small GTPases and affected cytoskeletal reorganization and synapse formation remains unclear. In this sudy, we reported that GGT mediates BDNF‐induced neuronal synaptogenesis through small GTPase Rac1 activation.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/jnc.12249</identifier><identifier>PMID: 23534605</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Alkyl and Aryl Transferases - physiology ; Animals ; Brain ; Brain-Derived Neurotrophic Factor - pharmacology ; Brain-Derived Neurotrophic Factor - physiology ; brain‐derived neurotrophic factor ; Cells, Cultured ; Gene expression ; geranylgeranyltransferase I ; Hippocampus - drug effects ; Hippocampus - enzymology ; Humans ; Neurogenesis - drug effects ; Neurogenesis - physiology ; Neurons ; post‐synaptic density protein 95 ; Rac ; rac1 GTP-Binding Protein - physiology ; Rats ; Rats, Sprague-Dawley ; Synapses - drug effects ; Synapses - enzymology ; Synapsin 1 ; synaptogenesis</subject><ispartof>Journal of neurochemistry, 2013-06, Vol.125 (5), p.698-712</ispartof><rights>2013 International Society for Neurochemistry</rights><rights>2013 International Society for Neurochemistry.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4879-4d33a322176f0179c8c4d85f8848d228a9dc01215b4eb11de0c4eaf47ed18a123</citedby><cites>FETCH-LOGICAL-c4879-4d33a322176f0179c8c4d85f8848d228a9dc01215b4eb11de0c4eaf47ed18a123</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/23534605$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Zhengwei</creatorcontrib><creatorcontrib>Sun, Chengdong</creatorcontrib><creatorcontrib>Zhang, Tao</creatorcontrib><creatorcontrib>Mo, Jianbing</creatorcontrib><creatorcontrib>Shi, Qiong</creatorcontrib><creatorcontrib>Zhang, Xianfeng</creatorcontrib><creatorcontrib>Yuan, Maochun</creatorcontrib><creatorcontrib>Chen, Long</creatorcontrib><creatorcontrib>Mao, Xueqiang</creatorcontrib><creatorcontrib>Yu, Rutong</creatorcontrib><creatorcontrib>Zhou, Xiuping</creatorcontrib><title>Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>Geranylgeranyltransferase I (GGT) is a prenyltransferase that mediates lipid modification of Rho small GTPases, such as Rho, Rac, and Cdc42, which are important for neuronal synaptogenesis. Although GGT is expressed in brain extensively, the function of GGT in central nerves system is largely unknown so far. We have previously demonstrated that GGT promotes the basal and neuronal activity and brain‐derived neurotrophic factor (BDNF)‐induced dendritic morphogenesis of cultured hippocampal neurons and cerebellar slices. This study is to explore the function and mechanism of GGT in neuronal synaptogenesis. We found that the protein level and activity of GGT gradually increased in rat hippocampus from P7 to P28 and subcellular located at synapse of neurons. The linear density of Synapsin 1 and post‐synaptic density protein 95 increased by over‐expression of GGT β, while reduced by inhibition or down‐regulation of GGT. In addition, GGT and its known substrate Rac was activated by BDNF, which promotes synaptogenesis in cultured hippocampal neurons. Furthermore, BDNF‐induced synaptogenesis was eliminated by GGT inhibition or down‐regulation, as well as by non‐prenylated Rac1 over‐expression. Together, our data suggested that GGT mediates BDNF‐induced neuronal synaptogenesis through Rac1 activation.
Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis
Synaptogenesis is a complicated process of interaction between extracellular factors, such BDNF, and intracellular signaling, such as Rho family small GTPases. However, the mechanism that BDNF activated Rho family small GTPases and affected cytoskeletal reorganization and synapse formation remains unclear. In this sudy, we reported that GGT mediates BDNF‐induced neuronal synaptogenesis through small GTPase Rac1 activation.</description><subject>Alkyl and Aryl Transferases - physiology</subject><subject>Animals</subject><subject>Brain</subject><subject>Brain-Derived Neurotrophic Factor - pharmacology</subject><subject>Brain-Derived Neurotrophic Factor - physiology</subject><subject>brain‐derived neurotrophic factor</subject><subject>Cells, Cultured</subject><subject>Gene expression</subject><subject>geranylgeranyltransferase I</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - enzymology</subject><subject>Humans</subject><subject>Neurogenesis - drug effects</subject><subject>Neurogenesis - physiology</subject><subject>Neurons</subject><subject>post‐synaptic density protein 95</subject><subject>Rac</subject><subject>rac1 GTP-Binding Protein - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Synapses - drug effects</subject><subject>Synapses - enzymology</subject><subject>Synapsin 1</subject><subject>synaptogenesis</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqN0b1OwzAQB3ALgaAUBl4ARWKBIeCzL4kz0vKtqiwwR659QanSpMSNUDYegWfkSTCkMCAh4cF3w09_6e4YOwB-Cv6dzStzCkJgusEGgAmECFG6yQacCxFKjmKH7To35xxijGGb7QgZSYx5NGCja2p01ZVPfVn53-W-dxTcBguyhV6RC0YX06v317eisq0hG7iu0stV_UQVucLtsa1cl47213XIHq8uH8Y34eT--nZ8PgkNqiQN0UqppRCQxDmHJDXKoFVRrhQqK4TSqTUcBEQzpBmAJW6QdI4JWVAahByy4z532dTPLblVtiicobLUFdWty0DGCaYAEv9B_fxJmqD09OgXnddtU_lBvhQHjlx5ddIr09TONZRny6ZY6KbLgGefN8j8DbKvG3h7uE5sZ36DP_J76R6c9eClKKn7Oym7m477yA_wY48o</recordid><startdate>201306</startdate><enddate>201306</enddate><creator>Li, Zhengwei</creator><creator>Sun, Chengdong</creator><creator>Zhang, Tao</creator><creator>Mo, Jianbing</creator><creator>Shi, Qiong</creator><creator>Zhang, Xianfeng</creator><creator>Yuan, Maochun</creator><creator>Chen, Long</creator><creator>Mao, Xueqiang</creator><creator>Yu, Rutong</creator><creator>Zhou, Xiuping</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201306</creationdate><title>Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis</title><author>Li, Zhengwei ; Sun, Chengdong ; Zhang, Tao ; Mo, Jianbing ; Shi, Qiong ; Zhang, Xianfeng ; Yuan, Maochun ; Chen, Long ; Mao, Xueqiang ; Yu, Rutong ; Zhou, Xiuping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4879-4d33a322176f0179c8c4d85f8848d228a9dc01215b4eb11de0c4eaf47ed18a123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Alkyl and Aryl Transferases - physiology</topic><topic>Animals</topic><topic>Brain</topic><topic>Brain-Derived Neurotrophic Factor - pharmacology</topic><topic>Brain-Derived Neurotrophic Factor - physiology</topic><topic>brain‐derived neurotrophic factor</topic><topic>Cells, Cultured</topic><topic>Gene expression</topic><topic>geranylgeranyltransferase I</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - enzymology</topic><topic>Humans</topic><topic>Neurogenesis - drug effects</topic><topic>Neurogenesis - physiology</topic><topic>Neurons</topic><topic>post‐synaptic density protein 95</topic><topic>Rac</topic><topic>rac1 GTP-Binding Protein - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Synapses - drug effects</topic><topic>Synapses - enzymology</topic><topic>Synapsin 1</topic><topic>synaptogenesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Zhengwei</creatorcontrib><creatorcontrib>Sun, Chengdong</creatorcontrib><creatorcontrib>Zhang, Tao</creatorcontrib><creatorcontrib>Mo, Jianbing</creatorcontrib><creatorcontrib>Shi, Qiong</creatorcontrib><creatorcontrib>Zhang, Xianfeng</creatorcontrib><creatorcontrib>Yuan, Maochun</creatorcontrib><creatorcontrib>Chen, Long</creatorcontrib><creatorcontrib>Mao, Xueqiang</creatorcontrib><creatorcontrib>Yu, Rutong</creatorcontrib><creatorcontrib>Zhou, Xiuping</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Zhengwei</au><au>Sun, Chengdong</au><au>Zhang, Tao</au><au>Mo, Jianbing</au><au>Shi, Qiong</au><au>Zhang, Xianfeng</au><au>Yuan, Maochun</au><au>Chen, Long</au><au>Mao, Xueqiang</au><au>Yu, Rutong</au><au>Zhou, Xiuping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2013-06</date><risdate>2013</risdate><volume>125</volume><issue>5</issue><spage>698</spage><epage>712</epage><pages>698-712</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><abstract>Geranylgeranyltransferase I (GGT) is a prenyltransferase that mediates lipid modification of Rho small GTPases, such as Rho, Rac, and Cdc42, which are important for neuronal synaptogenesis. Although GGT is expressed in brain extensively, the function of GGT in central nerves system is largely unknown so far. We have previously demonstrated that GGT promotes the basal and neuronal activity and brain‐derived neurotrophic factor (BDNF)‐induced dendritic morphogenesis of cultured hippocampal neurons and cerebellar slices. This study is to explore the function and mechanism of GGT in neuronal synaptogenesis. We found that the protein level and activity of GGT gradually increased in rat hippocampus from P7 to P28 and subcellular located at synapse of neurons. The linear density of Synapsin 1 and post‐synaptic density protein 95 increased by over‐expression of GGT β, while reduced by inhibition or down‐regulation of GGT. In addition, GGT and its known substrate Rac was activated by BDNF, which promotes synaptogenesis in cultured hippocampal neurons. Furthermore, BDNF‐induced synaptogenesis was eliminated by GGT inhibition or down‐regulation, as well as by non‐prenylated Rac1 over‐expression. Together, our data suggested that GGT mediates BDNF‐induced neuronal synaptogenesis through Rac1 activation.
Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis
Synaptogenesis is a complicated process of interaction between extracellular factors, such BDNF, and intracellular signaling, such as Rho family small GTPases. However, the mechanism that BDNF activated Rho family small GTPases and affected cytoskeletal reorganization and synapse formation remains unclear. In this sudy, we reported that GGT mediates BDNF‐induced neuronal synaptogenesis through small GTPase Rac1 activation.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>23534605</pmid><doi>10.1111/jnc.12249</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alkyl and Aryl Transferases - physiology Animals Brain Brain-Derived Neurotrophic Factor - pharmacology Brain-Derived Neurotrophic Factor - physiology brain‐derived neurotrophic factor Cells, Cultured Gene expression geranylgeranyltransferase I Hippocampus - drug effects Hippocampus - enzymology Humans Neurogenesis - drug effects Neurogenesis - physiology Neurons post‐synaptic density protein 95 Rac rac1 GTP-Binding Protein - physiology Rats Rats, Sprague-Dawley Synapses - drug effects Synapses - enzymology Synapsin 1 synaptogenesis |
title | Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis |
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