Reward-Related Expectations Trigger Dendritic Spine Plasticity in the Mouse Ventrolateral Orbitofrontal Cortex
An essential aspect of goal-directed decision-making is selecting actions based on anticipated consequences, a process that involves the orbitofrontal cortex (OFC) and potentially, the plasticity of dendritic spines in this region. To investigate this possibility, we trained male and female mice to...
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description | An essential aspect of goal-directed decision-making is selecting actions based on anticipated consequences, a process that involves the orbitofrontal cortex (OFC) and potentially, the plasticity of dendritic spines in this region. To investigate this possibility, we trained male and female mice to nose poke for food reinforcers, or we delivered the same number of food reinforcers non-contingently to separate mice. We then decreased the likelihood of reinforcement for trained mice, requiring them to modify action-outcome expectations. In a separate experiment, we blocked action-outcome updating via chemogenetic inactivation of the OFC. In both cases, successfully selecting actions based on their likely consequences was associated with fewer immature, thin-shaped dendritic spines and a greater proportion of mature, mushroom-shaped spines in the ventrolateral OFC. This pattern was distinct from spine loss associated with aging, and we identified no effects on hippocampal CA1 neurons. Given that the OFC is involved in prospective calculations of likely outcomes, even when they are not observable, constraining spinogenesis while preserving mature spines may be important for solidifying durable expectations. To investigate causal relationships, we inhibited the RNA-binding protein fragile X mental retardation protein (encoded by
), which constrains dendritic spine turnover. Ventrolateral OFC-selective
knockdown recapitulated the behavioral effects of inducible OFC inactivation (and lesions; also shown here), impairing action-outcome conditioning, and caused dendritic spine excess. Our findings suggest that a proper balance of dendritic spine plasticity within the OFC is necessary for one's ability to select actions based on anticipated consequences.
Navigating a changing environment requires associating actions with their likely outcomes and updating these associations when they change. Dendritic spine plasticity is likely involved, yet relationships are unconfirmed. Using behavioral, chemogenetic, and viral-mediated gene silencing strategies and high-resolution microscopy, we find that modifying action-outcome expectations is associated with fewer immature spines and a greater proportion of mature spines in the ventrolateral orbitofrontal cortex (OFC). Given that the OFC is involved in prospectively calculating the likely outcomes of one's behavior, even when they are not observable, constraining spinogenesis while preserving mature spines may be important for |
doi_str_mv | 10.1523/JNEUROSCI.2031-18.2019 |
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), which constrains dendritic spine turnover. Ventrolateral OFC-selective
knockdown recapitulated the behavioral effects of inducible OFC inactivation (and lesions; also shown here), impairing action-outcome conditioning, and caused dendritic spine excess. Our findings suggest that a proper balance of dendritic spine plasticity within the OFC is necessary for one's ability to select actions based on anticipated consequences.
Navigating a changing environment requires associating actions with their likely outcomes and updating these associations when they change. Dendritic spine plasticity is likely involved, yet relationships are unconfirmed. Using behavioral, chemogenetic, and viral-mediated gene silencing strategies and high-resolution microscopy, we find that modifying action-outcome expectations is associated with fewer immature spines and a greater proportion of mature spines in the ventrolateral orbitofrontal cortex (OFC). Given that the OFC is involved in prospectively calculating the likely outcomes of one's behavior, even when they are not observable, constraining spinogenesis while preserving mature spines may be important for maintaining durable expectations.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.2031-18.2019</identifier><identifier>PMID: 30940719</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Aging ; Animals ; Anticipation, Psychological - physiology ; Behavioral plasticity ; Coding ; Conditioning, Operant ; Deactivation ; Decision Making ; Dendritic plasticity ; Dendritic spines ; Dendritic Spines - physiology ; Dendritic Spines - ultrastructure ; Dendritic structure ; Dependovirus - genetics ; Feeding Behavior ; Female ; FMR1 protein ; Food ; Fragile X Mental Retardation Protein - antagonists & inhibitors ; Fragile X Mental Retardation Protein - genetics ; Fragile X Mental Retardation Protein - physiology ; Fragile X syndrome ; Gene Knockdown Techniques ; Genes, Reporter ; Genetic Vectors - administration & dosage ; Hippocampus ; Inactivation ; Inhibition (psychology) ; Intellectual disabilities ; Lesions ; Male ; Mice ; Mice, Inbred C57BL ; Mushrooms ; Neuronal Plasticity - physiology ; Nose ; Optogenetics ; Plastic properties ; Plasticity ; Prefrontal Cortex - physiology ; Proteins ; Reinforcement ; Reinforcement, Psychology ; Reward ; Ribonucleic acid ; RNA ; RNA Interference ; RNA, Small Interfering - genetics ; RNA, Small Interfering - pharmacology ; RNA-binding protein ; Spine</subject><ispartof>The Journal of neuroscience, 2019-06, Vol.39 (23), p.4595-4605</ispartof><rights>Copyright © 2019 the authors.</rights><rights>Copyright Society for Neuroscience Jun 5, 2019</rights><rights>Copyright © 2019 the authors 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-9a587ab49dab3eeb6212560c16a26056cd6e4e5d3d7f9cc33cb2ac018c4532e23</citedby><orcidid>0000-0001-6057-2527</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/PMC6554633/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554633/$$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/30940719$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Whyte, Alonzo J</creatorcontrib><creatorcontrib>Kietzman, Henry W</creatorcontrib><creatorcontrib>Swanson, Andrew M</creatorcontrib><creatorcontrib>Butkovich, Laura M</creatorcontrib><creatorcontrib>Barbee, Britton R</creatorcontrib><creatorcontrib>Bassell, Gary J</creatorcontrib><creatorcontrib>Gross, Christina</creatorcontrib><creatorcontrib>Gourley, Shannon L</creatorcontrib><title>Reward-Related Expectations Trigger Dendritic Spine Plasticity in the Mouse Ventrolateral Orbitofrontal Cortex</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>An essential aspect of goal-directed decision-making is selecting actions based on anticipated consequences, a process that involves the orbitofrontal cortex (OFC) and potentially, the plasticity of dendritic spines in this region. To investigate this possibility, we trained male and female mice to nose poke for food reinforcers, or we delivered the same number of food reinforcers non-contingently to separate mice. We then decreased the likelihood of reinforcement for trained mice, requiring them to modify action-outcome expectations. In a separate experiment, we blocked action-outcome updating via chemogenetic inactivation of the OFC. In both cases, successfully selecting actions based on their likely consequences was associated with fewer immature, thin-shaped dendritic spines and a greater proportion of mature, mushroom-shaped spines in the ventrolateral OFC. This pattern was distinct from spine loss associated with aging, and we identified no effects on hippocampal CA1 neurons. Given that the OFC is involved in prospective calculations of likely outcomes, even when they are not observable, constraining spinogenesis while preserving mature spines may be important for solidifying durable expectations. To investigate causal relationships, we inhibited the RNA-binding protein fragile X mental retardation protein (encoded by
), which constrains dendritic spine turnover. Ventrolateral OFC-selective
knockdown recapitulated the behavioral effects of inducible OFC inactivation (and lesions; also shown here), impairing action-outcome conditioning, and caused dendritic spine excess. Our findings suggest that a proper balance of dendritic spine plasticity within the OFC is necessary for one's ability to select actions based on anticipated consequences.
Navigating a changing environment requires associating actions with their likely outcomes and updating these associations when they change. Dendritic spine plasticity is likely involved, yet relationships are unconfirmed. Using behavioral, chemogenetic, and viral-mediated gene silencing strategies and high-resolution microscopy, we find that modifying action-outcome expectations is associated with fewer immature spines and a greater proportion of mature spines in the ventrolateral orbitofrontal cortex (OFC). Given that the OFC is involved in prospectively calculating the likely outcomes of one's behavior, even when they are not observable, constraining spinogenesis while preserving mature spines may be important for maintaining durable expectations.</description><subject>Aging</subject><subject>Animals</subject><subject>Anticipation, Psychological - physiology</subject><subject>Behavioral plasticity</subject><subject>Coding</subject><subject>Conditioning, Operant</subject><subject>Deactivation</subject><subject>Decision Making</subject><subject>Dendritic plasticity</subject><subject>Dendritic spines</subject><subject>Dendritic Spines - physiology</subject><subject>Dendritic Spines - ultrastructure</subject><subject>Dendritic structure</subject><subject>Dependovirus - genetics</subject><subject>Feeding Behavior</subject><subject>Female</subject><subject>FMR1 protein</subject><subject>Food</subject><subject>Fragile X Mental Retardation Protein - antagonists & inhibitors</subject><subject>Fragile X Mental Retardation Protein - genetics</subject><subject>Fragile X Mental Retardation Protein - physiology</subject><subject>Fragile X syndrome</subject><subject>Gene Knockdown Techniques</subject><subject>Genes, Reporter</subject><subject>Genetic Vectors - administration & dosage</subject><subject>Hippocampus</subject><subject>Inactivation</subject><subject>Inhibition (psychology)</subject><subject>Intellectual disabilities</subject><subject>Lesions</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mushrooms</subject><subject>Neuronal Plasticity - physiology</subject><subject>Nose</subject><subject>Optogenetics</subject><subject>Plastic properties</subject><subject>Plasticity</subject><subject>Prefrontal Cortex - physiology</subject><subject>Proteins</subject><subject>Reinforcement</subject><subject>Reinforcement, Psychology</subject><subject>Reward</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA Interference</subject><subject>RNA, Small Interfering - genetics</subject><subject>RNA, Small Interfering - pharmacology</subject><subject>RNA-binding protein</subject><subject>Spine</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkVtvEzEQhS0EomnhL1SWeOFli--7-1IJpekFFYLSy6vl9U5SVxs7tR1o_329aomAp9FozpyZow-hQ0qOqGT8y7cfs5vF_Gp6ccQIpxVtSqXtGzQp07ZigtC3aEJYTSolarGH9lO6J4TUhNbv0R4nrSA1bSfIL-C3iX21gMFk6PHscQM2m-yCT_g6utUKIj4B30eXncVXG-cB_xxMKp3LT9h5nO8Afw_bBPgWfI5hNIpmwPPYuRyWMfhcummIGR4_oHdLMyT4-FoP0M3p7Hp6Xl3Ozy6mXy8rKwTLVWtkU5tOtL3pOECnGGVSEUuVYYpIZXsFAmTP-3rZWsu57ZixhDZWSM6A8QN0_OK72XZr6O34mBn0Jrq1iU86GKf_nXh3p1fhl1ZSCsV5Mfj8ahDDwxZS1muXLAyD8VCyasYIU6ph9Xjr03_S-7CNvsQrKt4qrhoui0q9qGwMKUVY7p6hRI9I9Q6pHpFq2ugRaVk8_DvKbu0PQ_4M0qegeA</recordid><startdate>20190605</startdate><enddate>20190605</enddate><creator>Whyte, Alonzo J</creator><creator>Kietzman, Henry W</creator><creator>Swanson, Andrew M</creator><creator>Butkovich, Laura M</creator><creator>Barbee, Britton R</creator><creator>Bassell, Gary J</creator><creator>Gross, Christina</creator><creator>Gourley, Shannon L</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/0000-0001-6057-2527</orcidid></search><sort><creationdate>20190605</creationdate><title>Reward-Related Expectations Trigger Dendritic Spine Plasticity in the Mouse Ventrolateral Orbitofrontal Cortex</title><author>Whyte, Alonzo J ; Kietzman, Henry W ; Swanson, Andrew M ; Butkovich, Laura M ; Barbee, Britton R ; Bassell, Gary J ; Gross, Christina ; Gourley, Shannon L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-9a587ab49dab3eeb6212560c16a26056cd6e4e5d3d7f9cc33cb2ac018c4532e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aging</topic><topic>Animals</topic><topic>Anticipation, Psychological - physiology</topic><topic>Behavioral plasticity</topic><topic>Coding</topic><topic>Conditioning, Operant</topic><topic>Deactivation</topic><topic>Decision Making</topic><topic>Dendritic plasticity</topic><topic>Dendritic spines</topic><topic>Dendritic Spines - physiology</topic><topic>Dendritic Spines - ultrastructure</topic><topic>Dendritic structure</topic><topic>Dependovirus - genetics</topic><topic>Feeding Behavior</topic><topic>Female</topic><topic>FMR1 protein</topic><topic>Food</topic><topic>Fragile X Mental Retardation Protein - antagonists & inhibitors</topic><topic>Fragile X Mental Retardation Protein - genetics</topic><topic>Fragile X Mental Retardation Protein - physiology</topic><topic>Fragile X syndrome</topic><topic>Gene Knockdown Techniques</topic><topic>Genes, Reporter</topic><topic>Genetic Vectors - administration & dosage</topic><topic>Hippocampus</topic><topic>Inactivation</topic><topic>Inhibition (psychology)</topic><topic>Intellectual disabilities</topic><topic>Lesions</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mushrooms</topic><topic>Neuronal Plasticity - physiology</topic><topic>Nose</topic><topic>Optogenetics</topic><topic>Plastic properties</topic><topic>Plasticity</topic><topic>Prefrontal Cortex - physiology</topic><topic>Proteins</topic><topic>Reinforcement</topic><topic>Reinforcement, Psychology</topic><topic>Reward</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA Interference</topic><topic>RNA, Small Interfering - genetics</topic><topic>RNA, Small Interfering - pharmacology</topic><topic>RNA-binding protein</topic><topic>Spine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Whyte, Alonzo J</creatorcontrib><creatorcontrib>Kietzman, Henry W</creatorcontrib><creatorcontrib>Swanson, Andrew M</creatorcontrib><creatorcontrib>Butkovich, Laura M</creatorcontrib><creatorcontrib>Barbee, Britton R</creatorcontrib><creatorcontrib>Bassell, Gary J</creatorcontrib><creatorcontrib>Gross, Christina</creatorcontrib><creatorcontrib>Gourley, Shannon L</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>Whyte, Alonzo J</au><au>Kietzman, Henry W</au><au>Swanson, Andrew M</au><au>Butkovich, Laura M</au><au>Barbee, Britton R</au><au>Bassell, Gary J</au><au>Gross, Christina</au><au>Gourley, Shannon L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reward-Related Expectations Trigger Dendritic Spine Plasticity in the Mouse Ventrolateral Orbitofrontal Cortex</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2019-06-05</date><risdate>2019</risdate><volume>39</volume><issue>23</issue><spage>4595</spage><epage>4605</epage><pages>4595-4605</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>An essential aspect of goal-directed decision-making is selecting actions based on anticipated consequences, a process that involves the orbitofrontal cortex (OFC) and potentially, the plasticity of dendritic spines in this region. To investigate this possibility, we trained male and female mice to nose poke for food reinforcers, or we delivered the same number of food reinforcers non-contingently to separate mice. We then decreased the likelihood of reinforcement for trained mice, requiring them to modify action-outcome expectations. In a separate experiment, we blocked action-outcome updating via chemogenetic inactivation of the OFC. In both cases, successfully selecting actions based on their likely consequences was associated with fewer immature, thin-shaped dendritic spines and a greater proportion of mature, mushroom-shaped spines in the ventrolateral OFC. This pattern was distinct from spine loss associated with aging, and we identified no effects on hippocampal CA1 neurons. Given that the OFC is involved in prospective calculations of likely outcomes, even when they are not observable, constraining spinogenesis while preserving mature spines may be important for solidifying durable expectations. To investigate causal relationships, we inhibited the RNA-binding protein fragile X mental retardation protein (encoded by
), which constrains dendritic spine turnover. Ventrolateral OFC-selective
knockdown recapitulated the behavioral effects of inducible OFC inactivation (and lesions; also shown here), impairing action-outcome conditioning, and caused dendritic spine excess. Our findings suggest that a proper balance of dendritic spine plasticity within the OFC is necessary for one's ability to select actions based on anticipated consequences.
Navigating a changing environment requires associating actions with their likely outcomes and updating these associations when they change. Dendritic spine plasticity is likely involved, yet relationships are unconfirmed. Using behavioral, chemogenetic, and viral-mediated gene silencing strategies and high-resolution microscopy, we find that modifying action-outcome expectations is associated with fewer immature spines and a greater proportion of mature spines in the ventrolateral orbitofrontal cortex (OFC). Given that the OFC is involved in prospectively calculating the likely outcomes of one's behavior, even when they are not observable, constraining spinogenesis while preserving mature spines may be important for maintaining durable expectations.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>30940719</pmid><doi>10.1523/JNEUROSCI.2031-18.2019</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-6057-2527</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aging Animals Anticipation, Psychological - physiology Behavioral plasticity Coding Conditioning, Operant Deactivation Decision Making Dendritic plasticity Dendritic spines Dendritic Spines - physiology Dendritic Spines - ultrastructure Dendritic structure Dependovirus - genetics Feeding Behavior Female FMR1 protein Food Fragile X Mental Retardation Protein - antagonists & inhibitors Fragile X Mental Retardation Protein - genetics Fragile X Mental Retardation Protein - physiology Fragile X syndrome Gene Knockdown Techniques Genes, Reporter Genetic Vectors - administration & dosage Hippocampus Inactivation Inhibition (psychology) Intellectual disabilities Lesions Male Mice Mice, Inbred C57BL Mushrooms Neuronal Plasticity - physiology Nose Optogenetics Plastic properties Plasticity Prefrontal Cortex - physiology Proteins Reinforcement Reinforcement, Psychology Reward Ribonucleic acid RNA RNA Interference RNA, Small Interfering - genetics RNA, Small Interfering - pharmacology RNA-binding protein Spine |
title | Reward-Related Expectations Trigger Dendritic Spine Plasticity in the Mouse Ventrolateral Orbitofrontal Cortex |
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