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Sensory modality-specific homeostatic plasticity in the developing optic tectum
We describe a novel form of homeostatic synaptic plasticity in multisensory neurons in the optic tectum of Xenopus laevis tadpoles. Individual tectal neurons are known to receive converging inputs from multiple sensory modalities. We show that long-term alterations in either visual or mechanosensory...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415229/ https://www.ncbi.nlm.nih.gov/pubmed/21441922 http://dx.doi.org/10.1038/nn.2772 |
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author | Deeg, Katherine E. Aizenman, Carlos D. |
author_facet | Deeg, Katherine E. Aizenman, Carlos D. |
author_sort | Deeg, Katherine E. |
collection | PubMed |
description | We describe a novel form of homeostatic synaptic plasticity in multisensory neurons in the optic tectum of Xenopus laevis tadpoles. Individual tectal neurons are known to receive converging inputs from multiple sensory modalities. We show that long-term alterations in either visual or mechanosensory activity in vivo result in homeostatic changes specific to each sensory modality. In contrast to typical forms of homeostatic synaptic plasticity, such as synaptic scaling, we show that this type of plasticity occurs in a pathway-specific manner more reminiscent of Hebbian-type plasticity. |
format | Online Article Text |
id | pubmed-3415229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
record_format | MEDLINE/PubMed |
spelling | pubmed-34152292012-08-09 Sensory modality-specific homeostatic plasticity in the developing optic tectum Deeg, Katherine E. Aizenman, Carlos D. Nat Neurosci Article We describe a novel form of homeostatic synaptic plasticity in multisensory neurons in the optic tectum of Xenopus laevis tadpoles. Individual tectal neurons are known to receive converging inputs from multiple sensory modalities. We show that long-term alterations in either visual or mechanosensory activity in vivo result in homeostatic changes specific to each sensory modality. In contrast to typical forms of homeostatic synaptic plasticity, such as synaptic scaling, we show that this type of plasticity occurs in a pathway-specific manner more reminiscent of Hebbian-type plasticity. 2011-03-27 2011-05 /pmc/articles/PMC3415229/ /pubmed/21441922 http://dx.doi.org/10.1038/nn.2772 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Deeg, Katherine E. Aizenman, Carlos D. Sensory modality-specific homeostatic plasticity in the developing optic tectum |
title | Sensory modality-specific homeostatic plasticity in the developing optic tectum |
title_full | Sensory modality-specific homeostatic plasticity in the developing optic tectum |
title_fullStr | Sensory modality-specific homeostatic plasticity in the developing optic tectum |
title_full_unstemmed | Sensory modality-specific homeostatic plasticity in the developing optic tectum |
title_short | Sensory modality-specific homeostatic plasticity in the developing optic tectum |
title_sort | sensory modality-specific homeostatic plasticity in the developing optic tectum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415229/ https://www.ncbi.nlm.nih.gov/pubmed/21441922 http://dx.doi.org/10.1038/nn.2772 |
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