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Brain plasticity following corpus callosum agenesis or loss: a review of the Probst bundles
The corpus callosum is the largest axonal tract in the human brain, connecting the left and right cortical hemipheres. This structure is affected in myriad human neurodevelopmental disorders, and can be entirely absent as a result of congenital or surgical causes. The age when callosal loss occurs,...
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Published in: | Frontiers in neuroanatomy 2023-11, Vol.17, p.1296779 |
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description | The corpus callosum is the largest axonal tract in the human brain, connecting the left and right cortical hemipheres. This structure is affected in myriad human neurodevelopmental disorders, and can be entirely absent as a result of congenital or surgical causes. The age when callosal loss occurs, for example via surgical section in cases of refractory epilepsy, correlates with resulting brain morphology and neuropsychological outcomes, whereby an earlier loss generally produces relatively improved interhemispheric connectivity compared to a loss in adulthood (known as the "Sperry's paradox"). However, the mechanisms behind these age-dependent differences remain unclear. Perhaps the best documented and most striking of the plastic changes that occur due to developmental, but not adult, callosal loss is the formation of large, bilateral, longitudinal ectopic tracts termed Probst bundles. Despite over 100 years of research into these ectopic tracts, which are the largest and best described stereotypical ectopic brain tracts in humans, much remains unclear about them. Here, we review the anatomy of the Probst bundles, along with evidence for their faciliatory or detrimental function, the required conditions for their formation, patterns of etiology, and mechanisms of development. We provide hypotheses for many of the remaining mysteries of the Probst bundles, including their possible relationship to preserved interhemispheric communication following corpus callosum absence. Future research into naturally occurring plastic tracts such as Probst bundles will help to inform the general rules governing axon plasticity and disorders of brain miswiring. |
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This structure is affected in myriad human neurodevelopmental disorders, and can be entirely absent as a result of congenital or surgical causes. The age when callosal loss occurs, for example via surgical section in cases of refractory epilepsy, correlates with resulting brain morphology and neuropsychological outcomes, whereby an earlier loss generally produces relatively improved interhemispheric connectivity compared to a loss in adulthood (known as the "Sperry's paradox"). However, the mechanisms behind these age-dependent differences remain unclear. Perhaps the best documented and most striking of the plastic changes that occur due to developmental, but not adult, callosal loss is the formation of large, bilateral, longitudinal ectopic tracts termed Probst bundles. Despite over 100 years of research into these ectopic tracts, which are the largest and best described stereotypical ectopic brain tracts in humans, much remains unclear about them. Here, we review the anatomy of the Probst bundles, along with evidence for their faciliatory or detrimental function, the required conditions for their formation, patterns of etiology, and mechanisms of development. We provide hypotheses for many of the remaining mysteries of the Probst bundles, including their possible relationship to preserved interhemispheric communication following corpus callosum absence. Future research into naturally occurring plastic tracts such as Probst bundles will help to inform the general rules governing axon plasticity and disorders of brain miswiring.</description><identifier>ISSN: 1662-5129</identifier><identifier>EISSN: 1662-5129</identifier><identifier>DOI: 10.3389/fnana.2023.1296779</identifier><identifier>PMID: 38020213</identifier><language>eng</language><publisher>Switzerland: Frontiers Research Foundation</publisher><subject>Brain ; brain development ; callosotomy ; Cell death ; Cerebral hemispheres ; commissurotomy ; Corpus callosum ; Epilepsy ; Etiology ; interhemispheric communication ; Interhemispheric transfer ; Neural networks ; Neurodevelopmental disorders ; neurodevelopmental plasticity ; Neurons ; Neuroplasticity ; Neuropsychology ; split brain</subject><ispartof>Frontiers in neuroanatomy, 2023-11, Vol.17, p.1296779</ispartof><rights>Copyright © 2023 Lynton, Suárez and Fenlon.</rights><rights>2023. 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This structure is affected in myriad human neurodevelopmental disorders, and can be entirely absent as a result of congenital or surgical causes. The age when callosal loss occurs, for example via surgical section in cases of refractory epilepsy, correlates with resulting brain morphology and neuropsychological outcomes, whereby an earlier loss generally produces relatively improved interhemispheric connectivity compared to a loss in adulthood (known as the "Sperry's paradox"). However, the mechanisms behind these age-dependent differences remain unclear. Perhaps the best documented and most striking of the plastic changes that occur due to developmental, but not adult, callosal loss is the formation of large, bilateral, longitudinal ectopic tracts termed Probst bundles. Despite over 100 years of research into these ectopic tracts, which are the largest and best described stereotypical ectopic brain tracts in humans, much remains unclear about them. Here, we review the anatomy of the Probst bundles, along with evidence for their faciliatory or detrimental function, the required conditions for their formation, patterns of etiology, and mechanisms of development. We provide hypotheses for many of the remaining mysteries of the Probst bundles, including their possible relationship to preserved interhemispheric communication following corpus callosum absence. Future research into naturally occurring plastic tracts such as Probst bundles will help to inform the general rules governing axon plasticity and disorders of brain miswiring.</description><subject>Brain</subject><subject>brain development</subject><subject>callosotomy</subject><subject>Cell death</subject><subject>Cerebral hemispheres</subject><subject>commissurotomy</subject><subject>Corpus callosum</subject><subject>Epilepsy</subject><subject>Etiology</subject><subject>interhemispheric communication</subject><subject>Interhemispheric transfer</subject><subject>Neural networks</subject><subject>Neurodevelopmental disorders</subject><subject>neurodevelopmental plasticity</subject><subject>Neurons</subject><subject>Neuroplasticity</subject><subject>Neuropsychology</subject><subject>split brain</subject><issn>1662-5129</issn><issn>1662-5129</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdUUtPGzEYtKpWhVL-QA_IUi-9JPXbXm6A-kBCag_tiYP1rR-po8062LtF_Ps6JEWIk-3RzPj7ZhD6QMmSc9N9jiOMsGSE8SVlndK6e4WOqVJsIdv79bP7EXpX65oQxZSUb9ERN6TJKD9Gt5cF0oi3A9QpuTQ94JiHId-ncYVdLtu5YgcNqPMGwyqMoaaKc8ENqecYcAl_U7jHOeLpT8A_S-7rhPt59EOo79GbCEMNp4fzBP3--uXX1ffFzY9v11cXNwsnBJ0WiirKQ_CcUMYUk7rrvSZRCu6N97GNDIZJKZkxvgMZIjDjtVPeEDBGEH6Crve-PsPabkvaQHmwGZJ9BHJZWShtuyFYEN5BJKCD7IVxwlDZ9VR3qsWhvWDN69Pea1vy3RzqZDepujAMMIY8V8tMJ3WLjuy-_fiCus5zGdumjWWUkEzRnSHbs1xpkZUQnwakxO5qtI812l2N9lBjE50drOd-E_yT5H9v_B-OCZfo</recordid><startdate>20231106</startdate><enddate>20231106</enddate><creator>Lynton, Zorana</creator><creator>Suárez, Rodrigo</creator><creator>Fenlon, Laura R</creator><general>Frontiers Research Foundation</general><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</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>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20231106</creationdate><title>Brain plasticity following corpus callosum agenesis or loss: a review of the Probst bundles</title><author>Lynton, Zorana ; Suárez, Rodrigo ; Fenlon, Laura R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-61613eed3012262579bd70f543d8ddf265a82555288d9a5efa28d7c6d80a88403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Brain</topic><topic>brain development</topic><topic>callosotomy</topic><topic>Cell death</topic><topic>Cerebral hemispheres</topic><topic>commissurotomy</topic><topic>Corpus callosum</topic><topic>Epilepsy</topic><topic>Etiology</topic><topic>interhemispheric communication</topic><topic>Interhemispheric transfer</topic><topic>Neural networks</topic><topic>Neurodevelopmental disorders</topic><topic>neurodevelopmental plasticity</topic><topic>Neurons</topic><topic>Neuroplasticity</topic><topic>Neuropsychology</topic><topic>split brain</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lynton, Zorana</creatorcontrib><creatorcontrib>Suárez, Rodrigo</creatorcontrib><creatorcontrib>Fenlon, Laura R</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content (ProQuest)</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 Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Directory of Open Access Journals</collection><jtitle>Frontiers in neuroanatomy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lynton, Zorana</au><au>Suárez, Rodrigo</au><au>Fenlon, Laura R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brain plasticity following corpus callosum agenesis or loss: a review of the Probst bundles</atitle><jtitle>Frontiers in neuroanatomy</jtitle><addtitle>Front Neuroanat</addtitle><date>2023-11-06</date><risdate>2023</risdate><volume>17</volume><spage>1296779</spage><pages>1296779-</pages><issn>1662-5129</issn><eissn>1662-5129</eissn><abstract>The corpus callosum is the largest axonal tract in the human brain, connecting the left and right cortical hemipheres. 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subjects | Brain brain development callosotomy Cell death Cerebral hemispheres commissurotomy Corpus callosum Epilepsy Etiology interhemispheric communication Interhemispheric transfer Neural networks Neurodevelopmental disorders neurodevelopmental plasticity Neurons Neuroplasticity Neuropsychology split brain |
title | Brain plasticity following corpus callosum agenesis or loss: a review of the Probst bundles |
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