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Disruption of the expression of the proprotein convertase PC7 reduces BDNF production and affects learning and memory in mice
PC7 belongs to the proprotein convertase family, whose members are implicated in the cleavage of secretory precursors. The in vivo function of PC7 is unknown. Herein, we find that the precursor proBDNF is processed into mature BDNF in COS-1 cells coexpressing proBDNF with either PC7 or Furin. Conver...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2013-10, Vol.110 (43), p.37362-37362 |
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creator | Wetsel, William C Rodriguiz, Ramona M Guillemot, Johann Rousselet, Estelle Essalmani, Rachid Kim, Il Hwan Bryant, Jesse C Marcinkiewicz, Jadwiga Desjardins, Roxane Day, Robert Constam, Daniel B Prat, Annik Seidah, Nabil G |
description | PC7 belongs to the proprotein convertase family, whose members are implicated in the cleavage of secretory precursors. The in vivo function of PC7 is unknown. Herein, we find that the precursor proBDNF is processed into mature BDNF in COS-1 cells coexpressing proBDNF with either PC7 or Furin. Conversely, the processing of proBDNF into BDNF is markedly reduced in the absence of either Furin or PC7 in mouse primary hepatocytes. In vivo we observe that BDNF and PC7 mRNAs are colocalized in mouse hippocampus and amygdala and that mature BDNF protein levels are reduced in these brain areas in PC7 KO mice but not in the hippocampus of PC1/3 KO mice. Various behavioral tests reveal that in PC7 KO mice spatial memory is intact and plasticity of responding is mildly abnormal. Episodic and emotional memories are severely impaired, but both are rescued with the tyrosine receptor kinase B agonist 7,8-dihydroxyflavone. Altogether, these results support an in vivo role for PC7 in the regulation of certain types of cognitive performance, in part via proBDNF processing. Because polymorphic variants of human PC7 are being characterized, it will be important in future studies to determine their effects on additional physiological and behavioral processes. [PUBLICATION ABSTRACT] |
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The in vivo function of PC7 is unknown. Herein, we find that the precursor proBDNF is processed into mature BDNF in COS-1 cells coexpressing proBDNF with either PC7 or Furin. Conversely, the processing of proBDNF into BDNF is markedly reduced in the absence of either Furin or PC7 in mouse primary hepatocytes. In vivo we observe that BDNF and PC7 mRNAs are colocalized in mouse hippocampus and amygdala and that mature BDNF protein levels are reduced in these brain areas in PC7 KO mice but not in the hippocampus of PC1/3 KO mice. Various behavioral tests reveal that in PC7 KO mice spatial memory is intact and plasticity of responding is mildly abnormal. Episodic and emotional memories are severely impaired, but both are rescued with the tyrosine receptor kinase B agonist 7,8-dihydroxyflavone. Altogether, these results support an in vivo role for PC7 in the regulation of certain types of cognitive performance, in part via proBDNF processing. Because polymorphic variants of human PC7 are being characterized, it will be important in future studies to determine their effects on additional physiological and behavioral processes. [PUBLICATION ABSTRACT]</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><language>eng</language><publisher>Washington: National Academy of Sciences</publisher><subject>Animal memory ; Brain ; Brain-derived neurotrophic factor ; Cells ; Gene expression ; Rodents</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2013-10, Vol.110 (43), p.37362-37362</ispartof><rights>Copyright National Academy of Sciences Oct 22, 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Wetsel, William C</creatorcontrib><creatorcontrib>Rodriguiz, Ramona M</creatorcontrib><creatorcontrib>Guillemot, Johann</creatorcontrib><creatorcontrib>Rousselet, Estelle</creatorcontrib><creatorcontrib>Essalmani, Rachid</creatorcontrib><creatorcontrib>Kim, Il Hwan</creatorcontrib><creatorcontrib>Bryant, Jesse C</creatorcontrib><creatorcontrib>Marcinkiewicz, Jadwiga</creatorcontrib><creatorcontrib>Desjardins, Roxane</creatorcontrib><creatorcontrib>Day, Robert</creatorcontrib><creatorcontrib>Constam, Daniel B</creatorcontrib><creatorcontrib>Prat, Annik</creatorcontrib><creatorcontrib>Seidah, Nabil G</creatorcontrib><title>Disruption of the expression of the proprotein convertase PC7 reduces BDNF production and affects learning and memory in mice</title><title>Proceedings of the National Academy of Sciences - PNAS</title><description>PC7 belongs to the proprotein convertase family, whose members are implicated in the cleavage of secretory precursors. The in vivo function of PC7 is unknown. Herein, we find that the precursor proBDNF is processed into mature BDNF in COS-1 cells coexpressing proBDNF with either PC7 or Furin. Conversely, the processing of proBDNF into BDNF is markedly reduced in the absence of either Furin or PC7 in mouse primary hepatocytes. In vivo we observe that BDNF and PC7 mRNAs are colocalized in mouse hippocampus and amygdala and that mature BDNF protein levels are reduced in these brain areas in PC7 KO mice but not in the hippocampus of PC1/3 KO mice. Various behavioral tests reveal that in PC7 KO mice spatial memory is intact and plasticity of responding is mildly abnormal. Episodic and emotional memories are severely impaired, but both are rescued with the tyrosine receptor kinase B agonist 7,8-dihydroxyflavone. Altogether, these results support an in vivo role for PC7 in the regulation of certain types of cognitive performance, in part via proBDNF processing. Because polymorphic variants of human PC7 are being characterized, it will be important in future studies to determine their effects on additional physiological and behavioral processes. [PUBLICATION ABSTRACT]</description><subject>Animal memory</subject><subject>Brain</subject><subject>Brain-derived neurotrophic factor</subject><subject>Cells</subject><subject>Gene expression</subject><subject>Rodents</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpdjk1LxDAQhoMouK7-h4AXL4WkzedRd11XWNTD3pcknWqXNqlJK3rwvxtXDyIMDPPy8Mx7hGaUaFoIpskxmhFSykKxkp2is5T2hBDNFZmhz2Wb4jSMbfA4NHh8AQzvQ4SU_iRDDHlGaD12wb9BHE0C_LSQOEI9OUj4Zvmw-sbydVAZX2PTNODGhDsw0bf--RD20If4gbOpbx2co5PGdAkufvccbVe328W62Dze3S-uN8UgKCkY06WsjXNSKENcWdUlE5Q7Yrjm2hoQxjhrrbKKWGDSOiqloo3TpQMlVTVHVz_a3PB1gjTu-jY56DrjIUxpR_MDUXJekYxe_kP3YYo-l8sUE0JJrnT1BQR1anU</recordid><startdate>20131022</startdate><enddate>20131022</enddate><creator>Wetsel, William C</creator><creator>Rodriguiz, Ramona M</creator><creator>Guillemot, Johann</creator><creator>Rousselet, Estelle</creator><creator>Essalmani, Rachid</creator><creator>Kim, Il Hwan</creator><creator>Bryant, Jesse C</creator><creator>Marcinkiewicz, Jadwiga</creator><creator>Desjardins, Roxane</creator><creator>Day, Robert</creator><creator>Constam, Daniel B</creator><creator>Prat, Annik</creator><creator>Seidah, Nabil G</creator><general>National Academy of Sciences</general><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20131022</creationdate><title>Disruption of the expression of the proprotein convertase PC7 reduces BDNF production and affects learning and memory in mice</title><author>Wetsel, William C ; 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subjects | Animal memory Brain Brain-derived neurotrophic factor Cells Gene expression Rodents |
title | Disruption of the expression of the proprotein convertase PC7 reduces BDNF production and affects learning and memory in mice |
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