The Immediate Early Gene Arc Is Not Required for Hippocampal Long-Term Potentiation
Memory consolidation is thought to occur through protein synthesis-dependent synaptic plasticity mechanisms such as long-term potentiation (LTP). Dynamic changes in gene expression and epigenetic modifications underlie the maintenance of LTP. Similar mechanisms may mediate the storage of memory. Key...
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creator | Kyrke-Smith, Madeleine Volk, Lenora J Cooke, Samuel F Bear, Mark F Huganir, Richard L Shepherd, Jason D |
description | Memory consolidation is thought to occur through protein synthesis-dependent synaptic plasticity mechanisms such as long-term potentiation (LTP). Dynamic changes in gene expression and epigenetic modifications underlie the maintenance of LTP. Similar mechanisms may mediate the storage of memory. Key plasticity genes, such as the immediate early gene
, are induced by learning and by LTP induction. Mice that lack Arc have severe deficits in memory consolidation, and Arc has been implicated in numerous other forms of synaptic plasticity, including long-term depression and cell-to-cell signaling. Here, we take a comprehensive approach to determine if Arc is necessary for hippocampal LTP in male and female mice. Using a variety of Arc knock-out (KO) lines, we found that germline Arc KO mice show no deficits in CA1 LTP induced by high-frequency stimulation and enhanced LTP induced by theta-burst stimulation. Temporally restricting the removal of Arc to adult animals and spatially restricting it to the CA1 using Arc conditional KO mice did not have an effect on any form of LTP. Similarly, acute application of Arc antisense oligodeoxynucleotides had no effect on hippocampal CA1 LTP. Finally, the maintenance of
LTP in the dentate gyrus of Arc KO mice was normal. We conclude that Arc is not necessary for hippocampal LTP and may mediate memory consolidation through alternative mechanisms.
The immediate early gene Arc is critical for maintenance of long-term memory. How Arc mediates this process remains unclear, but it has been proposed to sustain Hebbian synaptic potentiation, which is a key component of memory encoding. This form of plasticity is modeled experimentally by induction of LTP, which increases Arc mRNA and protein expression. However, mechanistic data implicates Arc in the endocytosis of AMPA-type glutamate receptors and the weakening of synapses. Here, we took a comprehensive approach to determine if Arc is necessary for hippocampal LTP. We find that Arc is not required for LTP maintenance and may regulate memory storage through alternative mechanisms. |
doi_str_mv | 10.1523/JNEUROSCI.0008-20.2021 |
format | Article |
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, are induced by learning and by LTP induction. Mice that lack Arc have severe deficits in memory consolidation, and Arc has been implicated in numerous other forms of synaptic plasticity, including long-term depression and cell-to-cell signaling. Here, we take a comprehensive approach to determine if Arc is necessary for hippocampal LTP in male and female mice. Using a variety of Arc knock-out (KO) lines, we found that germline Arc KO mice show no deficits in CA1 LTP induced by high-frequency stimulation and enhanced LTP induced by theta-burst stimulation. Temporally restricting the removal of Arc to adult animals and spatially restricting it to the CA1 using Arc conditional KO mice did not have an effect on any form of LTP. Similarly, acute application of Arc antisense oligodeoxynucleotides had no effect on hippocampal CA1 LTP. Finally, the maintenance of
LTP in the dentate gyrus of Arc KO mice was normal. We conclude that Arc is not necessary for hippocampal LTP and may mediate memory consolidation through alternative mechanisms.
The immediate early gene Arc is critical for maintenance of long-term memory. How Arc mediates this process remains unclear, but it has been proposed to sustain Hebbian synaptic potentiation, which is a key component of memory encoding. This form of plasticity is modeled experimentally by induction of LTP, which increases Arc mRNA and protein expression. However, mechanistic data implicates Arc in the endocytosis of AMPA-type glutamate receptors and the weakening of synapses. Here, we took a comprehensive approach to determine if Arc is necessary for hippocampal LTP. We find that Arc is not required for LTP maintenance and may regulate memory storage through alternative mechanisms.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.0008-20.2021</identifier><identifier>PMID: 33833081</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Animal memory ; Animals ; Antisense oligonucleotides ; CA1 Region, Hippocampal - physiology ; Consolidation ; Cytoskeletal Proteins - genetics ; Cytoskeletal Proteins - physiology ; Dentate gyrus ; Dentate Gyrus - physiology ; Electric Stimulation ; Epigenetics ; Female ; Gene expression ; Genes, Immediate-Early ; Germ Cells ; Hippocampus ; Hippocampus - physiology ; Long-term depression ; Long-term potentiation ; Long-Term Potentiation - genetics ; Long-Term Potentiation - physiology ; Maintenance ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Nerve Tissue Proteins - genetics ; Nerve Tissue Proteins - physiology ; Neuronal Plasticity - genetics ; Neuronal Plasticity - physiology ; Oligonucleotides, Antisense - pharmacology ; Plasticity ; Protein biosynthesis ; Protein synthesis ; Stimulation ; Synaptic plasticity ; Theta Rhythm</subject><ispartof>The Journal of neuroscience, 2021-05, Vol.41 (19), p.4202-4211</ispartof><rights>Copyright © 2021 the authors.</rights><rights>Copyright Society for Neuroscience May 12, 2021</rights><rights>Copyright © 2021 the authors 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-7ce9868cc89c993adc53dbdeb78504942e91e85e707a0a339e0e117f6fe4baf43</citedby><cites>FETCH-LOGICAL-c442t-7ce9868cc89c993adc53dbdeb78504942e91e85e707a0a339e0e117f6fe4baf43</cites><orcidid>0000-0001-9783-5183 ; 0000-0001-7384-8289 ; 0000-0001-7736-3131 ; 0000-0002-9903-2541</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143205/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143205/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33833081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kyrke-Smith, Madeleine</creatorcontrib><creatorcontrib>Volk, Lenora J</creatorcontrib><creatorcontrib>Cooke, Samuel F</creatorcontrib><creatorcontrib>Bear, Mark F</creatorcontrib><creatorcontrib>Huganir, Richard L</creatorcontrib><creatorcontrib>Shepherd, Jason D</creatorcontrib><title>The Immediate Early Gene Arc Is Not Required for Hippocampal Long-Term Potentiation</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>Memory consolidation is thought to occur through protein synthesis-dependent synaptic plasticity mechanisms such as long-term potentiation (LTP). Dynamic changes in gene expression and epigenetic modifications underlie the maintenance of LTP. Similar mechanisms may mediate the storage of memory. Key plasticity genes, such as the immediate early gene
, are induced by learning and by LTP induction. Mice that lack Arc have severe deficits in memory consolidation, and Arc has been implicated in numerous other forms of synaptic plasticity, including long-term depression and cell-to-cell signaling. Here, we take a comprehensive approach to determine if Arc is necessary for hippocampal LTP in male and female mice. Using a variety of Arc knock-out (KO) lines, we found that germline Arc KO mice show no deficits in CA1 LTP induced by high-frequency stimulation and enhanced LTP induced by theta-burst stimulation. Temporally restricting the removal of Arc to adult animals and spatially restricting it to the CA1 using Arc conditional KO mice did not have an effect on any form of LTP. Similarly, acute application of Arc antisense oligodeoxynucleotides had no effect on hippocampal CA1 LTP. Finally, the maintenance of
LTP in the dentate gyrus of Arc KO mice was normal. We conclude that Arc is not necessary for hippocampal LTP and may mediate memory consolidation through alternative mechanisms.
The immediate early gene Arc is critical for maintenance of long-term memory. How Arc mediates this process remains unclear, but it has been proposed to sustain Hebbian synaptic potentiation, which is a key component of memory encoding. This form of plasticity is modeled experimentally by induction of LTP, which increases Arc mRNA and protein expression. However, mechanistic data implicates Arc in the endocytosis of AMPA-type glutamate receptors and the weakening of synapses. Here, we took a comprehensive approach to determine if Arc is necessary for hippocampal LTP. We find that Arc is not required for LTP maintenance and may regulate memory storage through alternative mechanisms.</description><subject>Animal memory</subject><subject>Animals</subject><subject>Antisense oligonucleotides</subject><subject>CA1 Region, Hippocampal - physiology</subject><subject>Consolidation</subject><subject>Cytoskeletal Proteins - genetics</subject><subject>Cytoskeletal Proteins - physiology</subject><subject>Dentate gyrus</subject><subject>Dentate Gyrus - physiology</subject><subject>Electric Stimulation</subject><subject>Epigenetics</subject><subject>Female</subject><subject>Gene expression</subject><subject>Genes, Immediate-Early</subject><subject>Germ Cells</subject><subject>Hippocampus</subject><subject>Hippocampus - physiology</subject><subject>Long-term depression</subject><subject>Long-term potentiation</subject><subject>Long-Term Potentiation - genetics</subject><subject>Long-Term Potentiation - physiology</subject><subject>Maintenance</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nerve Tissue Proteins - physiology</subject><subject>Neuronal Plasticity - genetics</subject><subject>Neuronal Plasticity - physiology</subject><subject>Oligonucleotides, Antisense - pharmacology</subject><subject>Plasticity</subject><subject>Protein biosynthesis</subject><subject>Protein synthesis</subject><subject>Stimulation</subject><subject>Synaptic plasticity</subject><subject>Theta Rhythm</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1r3DAQhkVpabZp_0IQ9NKLt6MPW9KlEJZtsmVJSrI5C608Thxsy5HsQv59tSRd2p7mMM-8zMtDyBmDJSu5-Prjan13c3272iwBQBcclhw4e0MWeWsKLoG9JQvgCopKKnlCPqT0mEkFTL0nJ0JoIUCzBbndPSDd9D3WrZuQrl3snukFDkjPo6ebRK_CRG_waW4j1rQJkV624xi860fX0W0Y7osdxp7-DBMOU85ow_CRvGtcl_DT6zwld9_Xu9Vlsb2-2KzOt4WXkk-F8mh0pb3XxhsjXO1LUe9r3CtdgjSSo2GoS1SgHDghDAIyppqqQbl3jRSn5NtL7jjvcwGfH4ius2NsexefbXCt_XcztA_2PvyymknBocwBX14DYniaMU22b5PHrnMDhjlZXjLGhWG8yujn_9DHMMch18uUYJWpSnGgqhfKx5BSxOb4DAN78GaP3uzBm-VgD97y4dnfVY5nf0SJ30iwlKM</recordid><startdate>20210512</startdate><enddate>20210512</enddate><creator>Kyrke-Smith, Madeleine</creator><creator>Volk, Lenora J</creator><creator>Cooke, Samuel F</creator><creator>Bear, Mark F</creator><creator>Huganir, Richard L</creator><creator>Shepherd, Jason D</creator><general>Society for Neuroscience</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>7QG</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><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9783-5183</orcidid><orcidid>https://orcid.org/0000-0001-7384-8289</orcidid><orcidid>https://orcid.org/0000-0001-7736-3131</orcidid><orcidid>https://orcid.org/0000-0002-9903-2541</orcidid></search><sort><creationdate>20210512</creationdate><title>The Immediate Early Gene Arc Is Not Required for Hippocampal Long-Term Potentiation</title><author>Kyrke-Smith, Madeleine ; Volk, Lenora J ; Cooke, Samuel F ; Bear, Mark F ; Huganir, Richard L ; Shepherd, Jason D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-7ce9868cc89c993adc53dbdeb78504942e91e85e707a0a339e0e117f6fe4baf43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animal memory</topic><topic>Animals</topic><topic>Antisense oligonucleotides</topic><topic>CA1 Region, Hippocampal - physiology</topic><topic>Consolidation</topic><topic>Cytoskeletal Proteins - genetics</topic><topic>Cytoskeletal Proteins - physiology</topic><topic>Dentate gyrus</topic><topic>Dentate Gyrus - physiology</topic><topic>Electric Stimulation</topic><topic>Epigenetics</topic><topic>Female</topic><topic>Gene expression</topic><topic>Genes, Immediate-Early</topic><topic>Germ Cells</topic><topic>Hippocampus</topic><topic>Hippocampus - physiology</topic><topic>Long-term depression</topic><topic>Long-term potentiation</topic><topic>Long-Term Potentiation - genetics</topic><topic>Long-Term Potentiation - physiology</topic><topic>Maintenance</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Nerve Tissue Proteins - physiology</topic><topic>Neuronal Plasticity - genetics</topic><topic>Neuronal Plasticity - physiology</topic><topic>Oligonucleotides, Antisense - pharmacology</topic><topic>Plasticity</topic><topic>Protein biosynthesis</topic><topic>Protein synthesis</topic><topic>Stimulation</topic><topic>Synaptic plasticity</topic><topic>Theta Rhythm</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kyrke-Smith, Madeleine</creatorcontrib><creatorcontrib>Volk, Lenora J</creatorcontrib><creatorcontrib>Cooke, Samuel F</creatorcontrib><creatorcontrib>Bear, Mark F</creatorcontrib><creatorcontrib>Huganir, Richard L</creatorcontrib><creatorcontrib>Shepherd, Jason D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kyrke-Smith, Madeleine</au><au>Volk, Lenora J</au><au>Cooke, Samuel F</au><au>Bear, Mark F</au><au>Huganir, Richard L</au><au>Shepherd, Jason D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Immediate Early Gene Arc Is Not Required for Hippocampal Long-Term Potentiation</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2021-05-12</date><risdate>2021</risdate><volume>41</volume><issue>19</issue><spage>4202</spage><epage>4211</epage><pages>4202-4211</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>Memory consolidation is thought to occur through protein synthesis-dependent synaptic plasticity mechanisms such as long-term potentiation (LTP). Dynamic changes in gene expression and epigenetic modifications underlie the maintenance of LTP. Similar mechanisms may mediate the storage of memory. Key plasticity genes, such as the immediate early gene
, are induced by learning and by LTP induction. Mice that lack Arc have severe deficits in memory consolidation, and Arc has been implicated in numerous other forms of synaptic plasticity, including long-term depression and cell-to-cell signaling. Here, we take a comprehensive approach to determine if Arc is necessary for hippocampal LTP in male and female mice. Using a variety of Arc knock-out (KO) lines, we found that germline Arc KO mice show no deficits in CA1 LTP induced by high-frequency stimulation and enhanced LTP induced by theta-burst stimulation. Temporally restricting the removal of Arc to adult animals and spatially restricting it to the CA1 using Arc conditional KO mice did not have an effect on any form of LTP. Similarly, acute application of Arc antisense oligodeoxynucleotides had no effect on hippocampal CA1 LTP. Finally, the maintenance of
LTP in the dentate gyrus of Arc KO mice was normal. We conclude that Arc is not necessary for hippocampal LTP and may mediate memory consolidation through alternative mechanisms.
The immediate early gene Arc is critical for maintenance of long-term memory. How Arc mediates this process remains unclear, but it has been proposed to sustain Hebbian synaptic potentiation, which is a key component of memory encoding. This form of plasticity is modeled experimentally by induction of LTP, which increases Arc mRNA and protein expression. However, mechanistic data implicates Arc in the endocytosis of AMPA-type glutamate receptors and the weakening of synapses. Here, we took a comprehensive approach to determine if Arc is necessary for hippocampal LTP. We find that Arc is not required for LTP maintenance and may regulate memory storage through alternative mechanisms.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>33833081</pmid><doi>10.1523/JNEUROSCI.0008-20.2021</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-9783-5183</orcidid><orcidid>https://orcid.org/0000-0001-7384-8289</orcidid><orcidid>https://orcid.org/0000-0001-7736-3131</orcidid><orcidid>https://orcid.org/0000-0002-9903-2541</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal memory Animals Antisense oligonucleotides CA1 Region, Hippocampal - physiology Consolidation Cytoskeletal Proteins - genetics Cytoskeletal Proteins - physiology Dentate gyrus Dentate Gyrus - physiology Electric Stimulation Epigenetics Female Gene expression Genes, Immediate-Early Germ Cells Hippocampus Hippocampus - physiology Long-term depression Long-term potentiation Long-Term Potentiation - genetics Long-Term Potentiation - physiology Maintenance Male Mice Mice, Inbred C57BL Mice, Knockout Nerve Tissue Proteins - genetics Nerve Tissue Proteins - physiology Neuronal Plasticity - genetics Neuronal Plasticity - physiology Oligonucleotides, Antisense - pharmacology Plasticity Protein biosynthesis Protein synthesis Stimulation Synaptic plasticity Theta Rhythm |
title | The Immediate Early Gene Arc Is Not Required for Hippocampal Long-Term Potentiation |
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