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Regional Regulation of Purkinje Cell Dendritic Spines by Integrins and Eph/Ephrins
Climbing fibres and parallel fibres compete for dendritic space on Purkinje cells in the cerebellum. Normally, climbing fibres populate the proximal dendrites, where they suppress the multiple small spines typical of parallel fibres, leading to their replacement by the few large spines that contact...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982633/ https://www.ncbi.nlm.nih.gov/pubmed/27518800 http://dx.doi.org/10.1371/journal.pone.0158558 |
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author | Heintz, Tristan G. Eva, Richard Fawcett, James W. |
author_facet | Heintz, Tristan G. Eva, Richard Fawcett, James W. |
author_sort | Heintz, Tristan G. |
collection | PubMed |
description | Climbing fibres and parallel fibres compete for dendritic space on Purkinje cells in the cerebellum. Normally, climbing fibres populate the proximal dendrites, where they suppress the multiple small spines typical of parallel fibres, leading to their replacement by the few large spines that contact climbing fibres. Previous work has shown that ephrins acting via EphA4 are a signal for this change in spine type and density. We have used an in vitro culture model in which to investigate the ephrin effect on Purkinje cell dendritic spines and the role of integrins in these changes. We found that integrins α3, α5 and β4 are present in many of the dendritic spines of cultured Purkinje cells. pFAK, the main downstream signalling molecule from integrins, has a similar distribution, although the intenstity of pFAK staining and the percentage of pFAK+ spines was consistently higher in the proximal dendrites. Activating integrins with Mg2+ led to an increase in the intensity of pFAK staining and an increase in the proportion of pFAK+ spines in both the proximal and distal dendrites, but no change in spine length, density or morphology. Blocking integrin binding with an RGD-containing peptide led to a reduction in spine length, with more stubby spines on both proximal and distal dendrites. Treatment of the cultures with ephrinA3-Fc chimera suppressed dendritic spines specifically on the proximal dendrites and there was also a decrease of pFAK in spines on this domain. This effect was blocked by simultaneous activation of integrins with Mn2+. We conclude that Eph/ephrin signaling regulates proximal dendritic spines in Purkinje cells by inactivating integrin downstream signalling. |
format | Online Article Text |
id | pubmed-4982633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49826332016-08-29 Regional Regulation of Purkinje Cell Dendritic Spines by Integrins and Eph/Ephrins Heintz, Tristan G. Eva, Richard Fawcett, James W. PLoS One Research Article Climbing fibres and parallel fibres compete for dendritic space on Purkinje cells in the cerebellum. Normally, climbing fibres populate the proximal dendrites, where they suppress the multiple small spines typical of parallel fibres, leading to their replacement by the few large spines that contact climbing fibres. Previous work has shown that ephrins acting via EphA4 are a signal for this change in spine type and density. We have used an in vitro culture model in which to investigate the ephrin effect on Purkinje cell dendritic spines and the role of integrins in these changes. We found that integrins α3, α5 and β4 are present in many of the dendritic spines of cultured Purkinje cells. pFAK, the main downstream signalling molecule from integrins, has a similar distribution, although the intenstity of pFAK staining and the percentage of pFAK+ spines was consistently higher in the proximal dendrites. Activating integrins with Mg2+ led to an increase in the intensity of pFAK staining and an increase in the proportion of pFAK+ spines in both the proximal and distal dendrites, but no change in spine length, density or morphology. Blocking integrin binding with an RGD-containing peptide led to a reduction in spine length, with more stubby spines on both proximal and distal dendrites. Treatment of the cultures with ephrinA3-Fc chimera suppressed dendritic spines specifically on the proximal dendrites and there was also a decrease of pFAK in spines on this domain. This effect was blocked by simultaneous activation of integrins with Mn2+. We conclude that Eph/ephrin signaling regulates proximal dendritic spines in Purkinje cells by inactivating integrin downstream signalling. Public Library of Science 2016-08-12 /pmc/articles/PMC4982633/ /pubmed/27518800 http://dx.doi.org/10.1371/journal.pone.0158558 Text en © 2016 Heintz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Heintz, Tristan G. Eva, Richard Fawcett, James W. Regional Regulation of Purkinje Cell Dendritic Spines by Integrins and Eph/Ephrins |
title | Regional Regulation of Purkinje Cell Dendritic Spines by Integrins and Eph/Ephrins |
title_full | Regional Regulation of Purkinje Cell Dendritic Spines by Integrins and Eph/Ephrins |
title_fullStr | Regional Regulation of Purkinje Cell Dendritic Spines by Integrins and Eph/Ephrins |
title_full_unstemmed | Regional Regulation of Purkinje Cell Dendritic Spines by Integrins and Eph/Ephrins |
title_short | Regional Regulation of Purkinje Cell Dendritic Spines by Integrins and Eph/Ephrins |
title_sort | regional regulation of purkinje cell dendritic spines by integrins and eph/ephrins |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982633/ https://www.ncbi.nlm.nih.gov/pubmed/27518800 http://dx.doi.org/10.1371/journal.pone.0158558 |
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