Impaired development and competitive refinement of the cortical frequency map in tumor necrosis factor-α-deficient mice
Early experience shapes sensory representations in a critical period of heightened plasticity. This adaptive process is thought to involve both Hebbian and homeostatic synaptic plasticity. Although Hebbian plasticity has been investigated as a mechanism for cortical map reorganization, less is known...
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Veröffentlicht in: | Cerebral cortex (New York, N.Y. 1991) N.Y. 1991), 2014-07, Vol.24 (7), p.1956-1965 |
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container_end_page | 1965 |
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container_issue | 7 |
container_start_page | 1956 |
container_title | Cerebral cortex (New York, N.Y. 1991) |
container_volume | 24 |
creator | Yang, Sungchil Zhang, Li S Gibboni, Robert Weiner, Benjamin Bao, Shaowen |
description | Early experience shapes sensory representations in a critical period of heightened plasticity. This adaptive process is thought to involve both Hebbian and homeostatic synaptic plasticity. Although Hebbian plasticity has been investigated as a mechanism for cortical map reorganization, less is known about the contribution of homeostatic plasticity. We investigated the role of homeostatic synaptic plasticity in the development and refinement of frequency representations in the primary auditory cortex using the tumor necrosis factor-α (TNF-α) knockout (KO), a mutant mouse with impaired homeostatic but normal Hebbian plasticity. Our results indicate that these mice develop weaker tonal responses and incomplete frequency representations. Rearing in a single-frequency revealed a normal expansion of cortical representations in KO mice. However, TNF-α KOs lacked homeostatic adjustments of cortical responses following exposure to multiple frequencies. Specifically, while this sensory over-stimulation resulted in competitive refinement of frequency tuning in wild-type controls, it broadened frequency tuning in TNF-α KOs. Our results suggest that homeostatic plasticity plays an important role in gain control and competitive interaction in sensory cortical development. |
doi_str_mv | 10.1093/cercor/bht053 |
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This adaptive process is thought to involve both Hebbian and homeostatic synaptic plasticity. Although Hebbian plasticity has been investigated as a mechanism for cortical map reorganization, less is known about the contribution of homeostatic plasticity. We investigated the role of homeostatic synaptic plasticity in the development and refinement of frequency representations in the primary auditory cortex using the tumor necrosis factor-α (TNF-α) knockout (KO), a mutant mouse with impaired homeostatic but normal Hebbian plasticity. Our results indicate that these mice develop weaker tonal responses and incomplete frequency representations. Rearing in a single-frequency revealed a normal expansion of cortical representations in KO mice. However, TNF-α KOs lacked homeostatic adjustments of cortical responses following exposure to multiple frequencies. Specifically, while this sensory over-stimulation resulted in competitive refinement of frequency tuning in wild-type controls, it broadened frequency tuning in TNF-α KOs. Our results suggest that homeostatic plasticity plays an important role in gain control and competitive interaction in sensory cortical development.</description><identifier>ISSN: 1047-3211</identifier><identifier>EISSN: 1460-2199</identifier><identifier>DOI: 10.1093/cercor/bht053</identifier><identifier>PMID: 23448874</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Acoustic Stimulation ; Age Factors ; Algorithms ; Analysis of Variance ; Animals ; Auditory Cortex - growth & development ; Auditory Cortex - pathology ; Auditory Cortex - physiopathology ; Auditory Perceptual Disorders - genetics ; Auditory Perceptual Disorders - pathology ; Auditory Perceptual Disorders - physiopathology ; Brain Mapping ; Critical Period (Psychology) ; Disease Models, Animal ; Environment ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Neuronal Plasticity - genetics ; Neuronal Plasticity - physiology ; Tumor Necrosis Factor-alpha - deficiency ; Tumor Necrosis Factor-alpha - genetics</subject><ispartof>Cerebral cortex (New York, N.Y. 1991), 2014-07, Vol.24 (7), p.1956-1965</ispartof><rights>The Author 2013. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.</rights><rights>The Author 2013. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23448874$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Sungchil</creatorcontrib><creatorcontrib>Zhang, Li S</creatorcontrib><creatorcontrib>Gibboni, Robert</creatorcontrib><creatorcontrib>Weiner, Benjamin</creatorcontrib><creatorcontrib>Bao, Shaowen</creatorcontrib><title>Impaired development and competitive refinement of the cortical frequency map in tumor necrosis factor-α-deficient mice</title><title>Cerebral cortex (New York, N.Y. 1991)</title><addtitle>Cereb Cortex</addtitle><description>Early experience shapes sensory representations in a critical period of heightened plasticity. This adaptive process is thought to involve both Hebbian and homeostatic synaptic plasticity. Although Hebbian plasticity has been investigated as a mechanism for cortical map reorganization, less is known about the contribution of homeostatic plasticity. We investigated the role of homeostatic synaptic plasticity in the development and refinement of frequency representations in the primary auditory cortex using the tumor necrosis factor-α (TNF-α) knockout (KO), a mutant mouse with impaired homeostatic but normal Hebbian plasticity. Our results indicate that these mice develop weaker tonal responses and incomplete frequency representations. Rearing in a single-frequency revealed a normal expansion of cortical representations in KO mice. However, TNF-α KOs lacked homeostatic adjustments of cortical responses following exposure to multiple frequencies. Specifically, while this sensory over-stimulation resulted in competitive refinement of frequency tuning in wild-type controls, it broadened frequency tuning in TNF-α KOs. Our results suggest that homeostatic plasticity plays an important role in gain control and competitive interaction in sensory cortical development.</description><subject>Acoustic Stimulation</subject><subject>Age Factors</subject><subject>Algorithms</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Auditory Cortex - growth & development</subject><subject>Auditory Cortex - pathology</subject><subject>Auditory Cortex - physiopathology</subject><subject>Auditory Perceptual Disorders - genetics</subject><subject>Auditory Perceptual Disorders - pathology</subject><subject>Auditory Perceptual Disorders - physiopathology</subject><subject>Brain Mapping</subject><subject>Critical Period (Psychology)</subject><subject>Disease Models, Animal</subject><subject>Environment</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Neuronal Plasticity - genetics</subject><subject>Neuronal Plasticity - physiology</subject><subject>Tumor Necrosis Factor-alpha - deficiency</subject><subject>Tumor Necrosis Factor-alpha - genetics</subject><issn>1047-3211</issn><issn>1460-2199</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctO3TAQhq0K1MOly24rL9mE43viTaUKUUBCYgPryJlMelzFcer4HMFj8SI8U01LK9ixmpH-X98_F0I-c3bKmZVrwAQxrbtNZlp-IAdcGVYJbu1e6ZmqKyk4X5HDZfnJGK-FFh_JSkilmqZWB-T-KszOJ-xpjzsc4xxwytRNPYUYZsw--x3ShIOf8I8UB5o3WNSUPbiRDgl_bXGCBxrcTP1E8zbERCeEFBe_0MFBjql6eqz6AgH_zAge8JjsD25c8NNLPSJ3389vzy6r65uLq7Nv19UsrM2VBCkbkMoMDDs3SNcxY4wG14kea9EYzbu64b1uGOdaDZaxxnIrQIIwpgN5RL7-5c7bLmAPJT-5sZ2TDy49tNH59q0y-U37I-5axcv5tC6AkxdAimXTJbfBL4Dj6CaM26XlWmtWok39DqvUgtXGqmL98nqs__P8-4z8DV_BlKQ</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Yang, Sungchil</creator><creator>Zhang, Li S</creator><creator>Gibboni, Robert</creator><creator>Weiner, Benjamin</creator><creator>Bao, Shaowen</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7QG</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20140701</creationdate><title>Impaired development and competitive refinement of the cortical frequency map in tumor necrosis factor-α-deficient mice</title><author>Yang, Sungchil ; Zhang, Li S ; Gibboni, Robert ; Weiner, Benjamin ; Bao, Shaowen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p299t-3c338c346f0ebaf3ab06665cab2de728651b781d5801154f90089192c3c266bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acoustic Stimulation</topic><topic>Age Factors</topic><topic>Algorithms</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Auditory Cortex - growth & development</topic><topic>Auditory Cortex - pathology</topic><topic>Auditory Cortex - physiopathology</topic><topic>Auditory Perceptual Disorders - genetics</topic><topic>Auditory Perceptual Disorders - pathology</topic><topic>Auditory Perceptual Disorders - physiopathology</topic><topic>Brain Mapping</topic><topic>Critical Period (Psychology)</topic><topic>Disease Models, Animal</topic><topic>Environment</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Neuronal Plasticity - genetics</topic><topic>Neuronal Plasticity - physiology</topic><topic>Tumor Necrosis Factor-alpha - deficiency</topic><topic>Tumor Necrosis Factor-alpha - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Sungchil</creatorcontrib><creatorcontrib>Zhang, Li S</creatorcontrib><creatorcontrib>Gibboni, Robert</creatorcontrib><creatorcontrib>Weiner, Benjamin</creatorcontrib><creatorcontrib>Bao, Shaowen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cerebral cortex (New York, N.Y. 1991)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Sungchil</au><au>Zhang, Li S</au><au>Gibboni, Robert</au><au>Weiner, Benjamin</au><au>Bao, Shaowen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impaired development and competitive refinement of the cortical frequency map in tumor necrosis factor-α-deficient mice</atitle><jtitle>Cerebral cortex (New York, N.Y. 1991)</jtitle><addtitle>Cereb Cortex</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>24</volume><issue>7</issue><spage>1956</spage><epage>1965</epage><pages>1956-1965</pages><issn>1047-3211</issn><eissn>1460-2199</eissn><abstract>Early experience shapes sensory representations in a critical period of heightened plasticity. This adaptive process is thought to involve both Hebbian and homeostatic synaptic plasticity. Although Hebbian plasticity has been investigated as a mechanism for cortical map reorganization, less is known about the contribution of homeostatic plasticity. We investigated the role of homeostatic synaptic plasticity in the development and refinement of frequency representations in the primary auditory cortex using the tumor necrosis factor-α (TNF-α) knockout (KO), a mutant mouse with impaired homeostatic but normal Hebbian plasticity. Our results indicate that these mice develop weaker tonal responses and incomplete frequency representations. Rearing in a single-frequency revealed a normal expansion of cortical representations in KO mice. However, TNF-α KOs lacked homeostatic adjustments of cortical responses following exposure to multiple frequencies. Specifically, while this sensory over-stimulation resulted in competitive refinement of frequency tuning in wild-type controls, it broadened frequency tuning in TNF-α KOs. Our results suggest that homeostatic plasticity plays an important role in gain control and competitive interaction in sensory cortical development.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>23448874</pmid><doi>10.1093/cercor/bht053</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection |
subjects | Acoustic Stimulation Age Factors Algorithms Analysis of Variance Animals Auditory Cortex - growth & development Auditory Cortex - pathology Auditory Cortex - physiopathology Auditory Perceptual Disorders - genetics Auditory Perceptual Disorders - pathology Auditory Perceptual Disorders - physiopathology Brain Mapping Critical Period (Psychology) Disease Models, Animal Environment Mice Mice, Inbred C57BL Mice, Knockout Neuronal Plasticity - genetics Neuronal Plasticity - physiology Tumor Necrosis Factor-alpha - deficiency Tumor Necrosis Factor-alpha - genetics |
title | Impaired development and competitive refinement of the cortical frequency map in tumor necrosis factor-α-deficient mice |
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