Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Journal of neurochemistry 2013-06, Vol.125 (5), p.698-712
Main Authors: Li, Zhengwei, Sun, Chengdong, Zhang, Tao, Mo, Jianbing, Shi, Qiong, Zhang, Xianfeng, Yuan, Maochun, Chen, Long, Mao, Xueqiang, Yu, Rutong, Zhou, Xiuping
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c4879-4d33a322176f0179c8c4d85f8848d228a9dc01215b4eb11de0c4eaf47ed18a123
cites cdi_FETCH-LOGICAL-c4879-4d33a322176f0179c8c4d85f8848d228a9dc01215b4eb11de0c4eaf47ed18a123
container_end_page 712
container_issue 5
container_start_page 698
container_title Journal of neurochemistry
container_volume 125
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1367491134</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1353479743</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4879-4d33a322176f0179c8c4d85f8848d228a9dc01215b4eb11de0c4eaf47ed18a123</originalsourceid><addsrcrecordid>eNqN0b1OwzAQB3ALgaAUBl4ARWKBIeCzL4kz0vKtqiwwR659QanSpMSNUDYegWfkSTCkMCAh4cF3w09_6e4YOwB-Cv6dzStzCkJgusEGgAmECFG6yQacCxFKjmKH7To35xxijGGb7QgZSYx5NGCja2p01ZVPfVn53-W-dxTcBguyhV6RC0YX06v317eisq0hG7iu0stV_UQVucLtsa1cl47213XIHq8uH8Y34eT--nZ8PgkNqiQN0UqppRCQxDmHJDXKoFVRrhQqK4TSqTUcBEQzpBmAJW6QdI4JWVAahByy4z532dTPLblVtiicobLUFdWty0DGCaYAEv9B_fxJmqD09OgXnddtU_lBvhQHjlx5ddIr09TONZRny6ZY6KbLgGefN8j8DbKvG3h7uE5sZ36DP_J76R6c9eClKKn7Oym7m477yA_wY48o</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1353010408</pqid></control><display><type>article</type><title>Geranylgeranyltransferase I mediates BDNF‐induced synaptogenesis</title><source>Wiley</source><source>Full-Text Journals in Chemistry (Open access)</source><creator>Li, Zhengwei ; Sun, Chengdong ; Zhang, Tao ; Mo, Jianbing ; Shi, Qiong ; Zhang, Xianfeng ; Yuan, Maochun ; Chen, Long ; Mao, Xueqiang ; Yu, Rutong ; Zhou, Xiuping</creator><creatorcontrib>Li, Zhengwei ; Sun, Chengdong ; Zhang, Tao ; Mo, Jianbing ; Shi, Qiong ; Zhang, Xianfeng ; Yuan, Maochun ; Chen, Long ; Mao, Xueqiang ; Yu, Rutong ; Zhou, Xiuping</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 0022-3042
ispartof Journal of neurochemistry, 2013-06, Vol.125 (5), p.698-712
issn 0022-3042
1471-4159
language eng
recordid cdi_proquest_miscellaneous_1367491134
source Wiley; Full-Text Journals in Chemistry (Open access)
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T21%3A28%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Geranylgeranyltransferase%20I%20mediates%20BDNF%E2%80%90induced%20synaptogenesis&rft.jtitle=Journal%20of%20neurochemistry&rft.au=Li,%20Zhengwei&rft.date=2013-06&rft.volume=125&rft.issue=5&rft.spage=698&rft.epage=712&rft.pages=698-712&rft.issn=0022-3042&rft.eissn=1471-4159&rft_id=info:doi/10.1111/jnc.12249&rft_dat=%3Cproquest_cross%3E1353479743%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4879-4d33a322176f0179c8c4d85f8848d228a9dc01215b4eb11de0c4eaf47ed18a123%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1353010408&rft_id=info:pmid/23534605&rfr_iscdi=true