The disorganized visual cortex in reelin-deficient mice is functional and allows for enhanced plasticity
A hallmark of neocortical circuits is the segregation of processing streams into six distinct layers. The importance of this layered organization for cortical processing and plasticity is little understood. We investigated the structure, function and plasticity of primary visual cortex (V1) of adult...
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description | A hallmark of neocortical circuits is the segregation of processing streams into six distinct layers. The importance of this layered organization for cortical processing and plasticity is little understood. We investigated the structure, function and plasticity of primary visual cortex (V1) of adult mice deficient for the glycoprotein reelin and their wild-type littermates. In V1 of
rl
−/− mice, cells with different laminar fates are present at all cortical depths. Surprisingly, the (vertically) disorganized cortex maintains a precise retinotopic (horizontal) organization.
Rl
−/− mice have normal basic visual capabilities, but are compromised in more challenging perceptual tasks, such as orientation discrimination. Additionally,
rl
−/− animals learn and memorize a visual task as well as their wild-type littermates. Interestingly, reelin deficiency enhances visual cortical plasticity: juvenile-like ocular dominance plasticity is preserved into late adulthood. The present data offer an important insight into the capabilities of a disorganized cortical system to maintain basic functional properties. |
doi_str_mv | 10.1007/s00429-014-0866-x |
format | Article |
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rl
−/− mice, cells with different laminar fates are present at all cortical depths. Surprisingly, the (vertically) disorganized cortex maintains a precise retinotopic (horizontal) organization.
Rl
−/− mice have normal basic visual capabilities, but are compromised in more challenging perceptual tasks, such as orientation discrimination. Additionally,
rl
−/− animals learn and memorize a visual task as well as their wild-type littermates. Interestingly, reelin deficiency enhances visual cortical plasticity: juvenile-like ocular dominance plasticity is preserved into late adulthood. The present data offer an important insight into the capabilities of a disorganized cortical system to maintain basic functional properties.</description><identifier>ISSN: 1863-2653</identifier><identifier>EISSN: 1863-2661</identifier><identifier>EISSN: 0340-2061</identifier><identifier>DOI: 10.1007/s00429-014-0866-x</identifier><identifier>PMID: 25119525</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Brain ; Cell Adhesion Molecules, Neuronal - genetics ; Cell Adhesion Molecules, Neuronal - metabolism ; Cell Biology ; Diazepam - pharmacology ; Discrimination (Psychology) - physiology ; Dominance, Ocular - drug effects ; Extracellular Matrix Proteins - genetics ; Extracellular Matrix Proteins - metabolism ; GABA Modulators - pharmacology ; Mice ; Molecules ; Nerve Net - cytology ; Nerve Tissue Proteins - genetics ; Nerve Tissue Proteins - metabolism ; Neurology ; Neuronal Plasticity ; Neurons ; Neurosciences ; Original ; Original Article ; Parvalbumins - metabolism ; Photic Stimulation ; Reinforcement (Psychology) ; Rodents ; Serine Endopeptidases - genetics ; Serine Endopeptidases - metabolism ; Visual Cortex - cytology ; Visual Cortex - metabolism ; Visual Cortex - physiology ; Visual Perception - physiology</subject><ispartof>Brain Structure and Function, 2015-11, Vol.220 (6), p.3449-3467</ispartof><rights>The Author(s) 2014</rights><rights>Springer-Verlag Berlin Heidelberg 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c639t-cf08f5b28339f0a6b9ee3d21cd8a181df8c328ea2fd5ad2cfc3dbe154e6e9f7a3</citedby><cites>FETCH-LOGICAL-c639t-cf08f5b28339f0a6b9ee3d21cd8a181df8c328ea2fd5ad2cfc3dbe154e6e9f7a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00429-014-0866-x$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00429-014-0866-x$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27903,27904,41467,42536,51298</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25119525$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pielecka-Fortuna, Justyna</creatorcontrib><creatorcontrib>Wagener, Robin Jan</creatorcontrib><creatorcontrib>Martens, Ann-Kristin</creatorcontrib><creatorcontrib>Goetze, Bianka</creatorcontrib><creatorcontrib>Schmidt, Karl-Friedrich</creatorcontrib><creatorcontrib>Staiger, Jochen F.</creatorcontrib><creatorcontrib>Löwel, Siegrid</creatorcontrib><title>The disorganized visual cortex in reelin-deficient mice is functional and allows for enhanced plasticity</title><title>Brain Structure and Function</title><addtitle>Brain Struct Funct</addtitle><addtitle>Brain Struct Funct</addtitle><description>A hallmark of neocortical circuits is the segregation of processing streams into six distinct layers. The importance of this layered organization for cortical processing and plasticity is little understood. We investigated the structure, function and plasticity of primary visual cortex (V1) of adult mice deficient for the glycoprotein reelin and their wild-type littermates. In V1 of
rl
−/− mice, cells with different laminar fates are present at all cortical depths. Surprisingly, the (vertically) disorganized cortex maintains a precise retinotopic (horizontal) organization.
Rl
−/− mice have normal basic visual capabilities, but are compromised in more challenging perceptual tasks, such as orientation discrimination. Additionally,
rl
−/− animals learn and memorize a visual task as well as their wild-type littermates. Interestingly, reelin deficiency enhances visual cortical plasticity: juvenile-like ocular dominance plasticity is preserved into late adulthood. The present data offer an important insight into the capabilities of a disorganized cortical system to maintain basic functional properties.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain</subject><subject>Cell Adhesion Molecules, Neuronal - genetics</subject><subject>Cell Adhesion Molecules, Neuronal - metabolism</subject><subject>Cell Biology</subject><subject>Diazepam - pharmacology</subject><subject>Discrimination (Psychology) - physiology</subject><subject>Dominance, Ocular - drug effects</subject><subject>Extracellular Matrix Proteins - genetics</subject><subject>Extracellular Matrix Proteins - metabolism</subject><subject>GABA Modulators - pharmacology</subject><subject>Mice</subject><subject>Molecules</subject><subject>Nerve Net - cytology</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neurology</subject><subject>Neuronal Plasticity</subject><subject>Neurons</subject><subject>Neurosciences</subject><subject>Original</subject><subject>Original Article</subject><subject>Parvalbumins - metabolism</subject><subject>Photic Stimulation</subject><subject>Reinforcement (Psychology)</subject><subject>Rodents</subject><subject>Serine Endopeptidases - genetics</subject><subject>Serine Endopeptidases - metabolism</subject><subject>Visual Cortex - cytology</subject><subject>Visual Cortex - metabolism</subject><subject>Visual Cortex - physiology</subject><subject>Visual Perception - physiology</subject><issn>1863-2653</issn><issn>1863-2661</issn><issn>0340-2061</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kU1vVCEUhonR2Hb0B7gxJG7cXOXjwsDGxDR-JU3c1DVh4DBDw8AI99Zpf71Mpk6qiQsC4Tzvew68CL2i5B0lZPm-ETIyPRA6DkRJOeyfoHOqJB-YlPTp6Sz4Gbpo7YYQoRXVz9EZE5RqwcQ52lxvAPvYSl3bHO_B49vYZpuwK3WCPY4ZV4AU8-AhRBchT3gbHeDYcJizm2LJnbbZY5tS-dVvS8WQNza7brZLtk1dNt29QM-CTQ1ePuwL9OPzp-vLr8PV9y_fLj9eDU5yPQ0uEBXEiinOdSBWrjQA94w6ryxV1AflOFNgWfDCeuaC434FVIwgQYel5Qv04ei7m1db8K4PXG0yuxq3tt6ZYqP5u5LjxqzLrRnFUkilu8HbB4Nafs7QJrONzUFKNkOZm6FLxqjiY18L9OYf9KbMtf_HgaJccaLEgaJHytXSWoVwGoYSc8jRHHM0PUdzyNHsu-b141ecFH-C6wA7Aq2X8hrqo9b_df0NNu2suQ</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Pielecka-Fortuna, Justyna</creator><creator>Wagener, Robin Jan</creator><creator>Martens, Ann-Kristin</creator><creator>Goetze, Bianka</creator><creator>Schmidt, Karl-Friedrich</creator><creator>Staiger, Jochen F.</creator><creator>Löwel, Siegrid</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>20151101</creationdate><title>The disorganized visual cortex in reelin-deficient mice is functional and allows for enhanced plasticity</title><author>Pielecka-Fortuna, Justyna ; Wagener, Robin Jan ; Martens, Ann-Kristin ; Goetze, Bianka ; Schmidt, Karl-Friedrich ; Staiger, Jochen F. ; Löwel, Siegrid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c639t-cf08f5b28339f0a6b9ee3d21cd8a181df8c328ea2fd5ad2cfc3dbe154e6e9f7a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain</topic><topic>Cell Adhesion Molecules, Neuronal - genetics</topic><topic>Cell Adhesion Molecules, Neuronal - metabolism</topic><topic>Cell Biology</topic><topic>Diazepam - pharmacology</topic><topic>Discrimination (Psychology) - physiology</topic><topic>Dominance, Ocular - drug effects</topic><topic>Extracellular Matrix Proteins - genetics</topic><topic>Extracellular Matrix Proteins - metabolism</topic><topic>GABA Modulators - pharmacology</topic><topic>Mice</topic><topic>Molecules</topic><topic>Nerve Net - cytology</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Neurology</topic><topic>Neuronal Plasticity</topic><topic>Neurons</topic><topic>Neurosciences</topic><topic>Original</topic><topic>Original Article</topic><topic>Parvalbumins - metabolism</topic><topic>Photic Stimulation</topic><topic>Reinforcement (Psychology)</topic><topic>Rodents</topic><topic>Serine Endopeptidases - genetics</topic><topic>Serine Endopeptidases - metabolism</topic><topic>Visual Cortex - cytology</topic><topic>Visual Cortex - metabolism</topic><topic>Visual Cortex - physiology</topic><topic>Visual Perception - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pielecka-Fortuna, Justyna</creatorcontrib><creatorcontrib>Wagener, Robin Jan</creatorcontrib><creatorcontrib>Martens, Ann-Kristin</creatorcontrib><creatorcontrib>Goetze, Bianka</creatorcontrib><creatorcontrib>Schmidt, Karl-Friedrich</creatorcontrib><creatorcontrib>Staiger, Jochen F.</creatorcontrib><creatorcontrib>Löwel, Siegrid</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Neurosciences Abstracts</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Psychology Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Brain Structure and Function</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pielecka-Fortuna, Justyna</au><au>Wagener, Robin Jan</au><au>Martens, Ann-Kristin</au><au>Goetze, Bianka</au><au>Schmidt, Karl-Friedrich</au><au>Staiger, Jochen F.</au><au>Löwel, Siegrid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The disorganized visual cortex in reelin-deficient mice is functional and allows for enhanced plasticity</atitle><jtitle>Brain Structure and Function</jtitle><stitle>Brain Struct Funct</stitle><addtitle>Brain Struct Funct</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>220</volume><issue>6</issue><spage>3449</spage><epage>3467</epage><pages>3449-3467</pages><issn>1863-2653</issn><eissn>1863-2661</eissn><eissn>0340-2061</eissn><abstract>A hallmark of neocortical circuits is the segregation of processing streams into six distinct layers. The importance of this layered organization for cortical processing and plasticity is little understood. We investigated the structure, function and plasticity of primary visual cortex (V1) of adult mice deficient for the glycoprotein reelin and their wild-type littermates. In V1 of
rl
−/− mice, cells with different laminar fates are present at all cortical depths. Surprisingly, the (vertically) disorganized cortex maintains a precise retinotopic (horizontal) organization.
Rl
−/− mice have normal basic visual capabilities, but are compromised in more challenging perceptual tasks, such as orientation discrimination. Additionally,
rl
−/− animals learn and memorize a visual task as well as their wild-type littermates. Interestingly, reelin deficiency enhances visual cortical plasticity: juvenile-like ocular dominance plasticity is preserved into late adulthood. The present data offer an important insight into the capabilities of a disorganized cortical system to maintain basic functional properties.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>25119525</pmid><doi>10.1007/s00429-014-0866-x</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomedical and Life Sciences Biomedicine Brain Cell Adhesion Molecules, Neuronal - genetics Cell Adhesion Molecules, Neuronal - metabolism Cell Biology Diazepam - pharmacology Discrimination (Psychology) - physiology Dominance, Ocular - drug effects Extracellular Matrix Proteins - genetics Extracellular Matrix Proteins - metabolism GABA Modulators - pharmacology Mice Molecules Nerve Net - cytology Nerve Tissue Proteins - genetics Nerve Tissue Proteins - metabolism Neurology Neuronal Plasticity Neurons Neurosciences Original Original Article Parvalbumins - metabolism Photic Stimulation Reinforcement (Psychology) Rodents Serine Endopeptidases - genetics Serine Endopeptidases - metabolism Visual Cortex - cytology Visual Cortex - metabolism Visual Cortex - physiology Visual Perception - physiology |
title | The disorganized visual cortex in reelin-deficient mice is functional and allows for enhanced plasticity |
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