author_facet Triplett, Jason W.
Pfeiffenberger, Cory
Yamada, Jena
Stafford, Ben K.
Sweeney, Neal T.
Litke, Alan M.
Sher, Alexander
Koulakov, Alexei A.
Feldheim, David A.
Triplett, Jason W.
Pfeiffenberger, Cory
Yamada, Jena
Stafford, Ben K.
Sweeney, Neal T.
Litke, Alan M.
Sher, Alexander
Koulakov, Alexei A.
Feldheim, David A.
author Triplett, Jason W.
Pfeiffenberger, Cory
Yamada, Jena
Stafford, Ben K.
Sweeney, Neal T.
Litke, Alan M.
Sher, Alexander
Koulakov, Alexei A.
Feldheim, David A.
spellingShingle Triplett, Jason W.
Pfeiffenberger, Cory
Yamada, Jena
Stafford, Ben K.
Sweeney, Neal T.
Litke, Alan M.
Sher, Alexander
Koulakov, Alexei A.
Feldheim, David A.
Proceedings of the National Academy of Sciences
Competition is a driving force in topographic mapping
Multidisciplinary
author_sort triplett, jason w.
spelling Triplett, Jason W. Pfeiffenberger, Cory Yamada, Jena Stafford, Ben K. Sweeney, Neal T. Litke, Alan M. Sher, Alexander Koulakov, Alexei A. Feldheim, David A. 0027-8424 1091-6490 Proceedings of the National Academy of Sciences Multidisciplinary http://dx.doi.org/10.1073/pnas.1102834108 <jats:p>Topographic maps are the primary means of relaying spatial information in the brain. Understanding the mechanisms by which they form has been a goal of experimental and theoretical neuroscientists for decades. The projection of the retina to the superior colliculus (SC)/tectum has been an important model used to show that graded molecular cues and patterned retinal activity are required for topographic map formation. Additionally, interaxon competition has been suggested to play a role in topographic map formation; however, this view has been recently challenged. Here we present experimental and computational evidence demonstrating that interaxon competition for target space is necessary to establish topography. To test this hypothesis experimentally, we determined the nature of the retinocollicular projection in Math5 (Atoh7) mutant mice, which have severely reduced numbers of retinal ganglion cell inputs into the SC. We find that in these mice, retinal axons project to the anteromedialj portion of the SC where repulsion from ephrin-A ligands is minimized and where their attraction to the midline is maximized. This observation is consistent with the chemoaffinity model that relies on axon–axon competition as a mapping mechanism. We conclude that chemical labels plus neural activity cannot alone specify the retinocollicular projection; instead axon–axon competition is necessary to create a map. Finally, we present a mathematical model for topographic mapping that incorporates molecular labels, neural activity, and axon competition.</jats:p> Competition is a driving force in topographic mapping Proceedings of the National Academy of Sciences
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title Competition is a driving force in topographic mapping
title_unstemmed Competition is a driving force in topographic mapping
title_full Competition is a driving force in topographic mapping
title_fullStr Competition is a driving force in topographic mapping
title_full_unstemmed Competition is a driving force in topographic mapping
title_short Competition is a driving force in topographic mapping
title_sort competition is a driving force in topographic mapping
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.1102834108
publishDate 2011
physical 19060-19065
description <jats:p>Topographic maps are the primary means of relaying spatial information in the brain. Understanding the mechanisms by which they form has been a goal of experimental and theoretical neuroscientists for decades. The projection of the retina to the superior colliculus (SC)/tectum has been an important model used to show that graded molecular cues and patterned retinal activity are required for topographic map formation. Additionally, interaxon competition has been suggested to play a role in topographic map formation; however, this view has been recently challenged. Here we present experimental and computational evidence demonstrating that interaxon competition for target space is necessary to establish topography. To test this hypothesis experimentally, we determined the nature of the retinocollicular projection in Math5 (Atoh7) mutant mice, which have severely reduced numbers of retinal ganglion cell inputs into the SC. We find that in these mice, retinal axons project to the anteromedialj portion of the SC where repulsion from ephrin-A ligands is minimized and where their attraction to the midline is maximized. This observation is consistent with the chemoaffinity model that relies on axon–axon competition as a mapping mechanism. We conclude that chemical labels plus neural activity cannot alone specify the retinocollicular projection; instead axon–axon competition is necessary to create a map. Finally, we present a mathematical model for topographic mapping that incorporates molecular labels, neural activity, and axon competition.</jats:p>
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author Triplett, Jason W., Pfeiffenberger, Cory, Yamada, Jena, Stafford, Ben K., Sweeney, Neal T., Litke, Alan M., Sher, Alexander, Koulakov, Alexei A., Feldheim, David A.
author_facet Triplett, Jason W., Pfeiffenberger, Cory, Yamada, Jena, Stafford, Ben K., Sweeney, Neal T., Litke, Alan M., Sher, Alexander, Koulakov, Alexei A., Feldheim, David A., Triplett, Jason W., Pfeiffenberger, Cory, Yamada, Jena, Stafford, Ben K., Sweeney, Neal T., Litke, Alan M., Sher, Alexander, Koulakov, Alexei A., Feldheim, David A.
author_sort triplett, jason w.
container_issue 47
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container_title Proceedings of the National Academy of Sciences
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description <jats:p>Topographic maps are the primary means of relaying spatial information in the brain. Understanding the mechanisms by which they form has been a goal of experimental and theoretical neuroscientists for decades. The projection of the retina to the superior colliculus (SC)/tectum has been an important model used to show that graded molecular cues and patterned retinal activity are required for topographic map formation. Additionally, interaxon competition has been suggested to play a role in topographic map formation; however, this view has been recently challenged. Here we present experimental and computational evidence demonstrating that interaxon competition for target space is necessary to establish topography. To test this hypothesis experimentally, we determined the nature of the retinocollicular projection in Math5 (Atoh7) mutant mice, which have severely reduced numbers of retinal ganglion cell inputs into the SC. We find that in these mice, retinal axons project to the anteromedialj portion of the SC where repulsion from ephrin-A ligands is minimized and where their attraction to the midline is maximized. This observation is consistent with the chemoaffinity model that relies on axon–axon competition as a mapping mechanism. We conclude that chemical labels plus neural activity cannot alone specify the retinocollicular projection; instead axon–axon competition is necessary to create a map. Finally, we present a mathematical model for topographic mapping that incorporates molecular labels, neural activity, and axon competition.</jats:p>
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spelling Triplett, Jason W. Pfeiffenberger, Cory Yamada, Jena Stafford, Ben K. Sweeney, Neal T. Litke, Alan M. Sher, Alexander Koulakov, Alexei A. Feldheim, David A. 0027-8424 1091-6490 Proceedings of the National Academy of Sciences Multidisciplinary http://dx.doi.org/10.1073/pnas.1102834108 <jats:p>Topographic maps are the primary means of relaying spatial information in the brain. Understanding the mechanisms by which they form has been a goal of experimental and theoretical neuroscientists for decades. The projection of the retina to the superior colliculus (SC)/tectum has been an important model used to show that graded molecular cues and patterned retinal activity are required for topographic map formation. Additionally, interaxon competition has been suggested to play a role in topographic map formation; however, this view has been recently challenged. Here we present experimental and computational evidence demonstrating that interaxon competition for target space is necessary to establish topography. To test this hypothesis experimentally, we determined the nature of the retinocollicular projection in Math5 (Atoh7) mutant mice, which have severely reduced numbers of retinal ganglion cell inputs into the SC. We find that in these mice, retinal axons project to the anteromedialj portion of the SC where repulsion from ephrin-A ligands is minimized and where their attraction to the midline is maximized. This observation is consistent with the chemoaffinity model that relies on axon–axon competition as a mapping mechanism. We conclude that chemical labels plus neural activity cannot alone specify the retinocollicular projection; instead axon–axon competition is necessary to create a map. Finally, we present a mathematical model for topographic mapping that incorporates molecular labels, neural activity, and axon competition.</jats:p> Competition is a driving force in topographic mapping Proceedings of the National Academy of Sciences
spellingShingle Triplett, Jason W., Pfeiffenberger, Cory, Yamada, Jena, Stafford, Ben K., Sweeney, Neal T., Litke, Alan M., Sher, Alexander, Koulakov, Alexei A., Feldheim, David A., Proceedings of the National Academy of Sciences, Competition is a driving force in topographic mapping, Multidisciplinary
title Competition is a driving force in topographic mapping
title_full Competition is a driving force in topographic mapping
title_fullStr Competition is a driving force in topographic mapping
title_full_unstemmed Competition is a driving force in topographic mapping
title_short Competition is a driving force in topographic mapping
title_sort competition is a driving force in topographic mapping
title_unstemmed Competition is a driving force in topographic mapping
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.1102834108