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Neuronal merlin influences ERBB2 receptor expression on Schwann cells through neuregulin 1 type III signalling
Axonal surface proteins encompass a group of heterogeneous molecules, which exert a variety of different functions in the highly interdependent relationship between axons and Schwann cells. We recently revealed that the tumour suppressor protein merlin, mutated in the hereditary tumour syndrome neur...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914471/ https://www.ncbi.nlm.nih.gov/pubmed/24309211 http://dx.doi.org/10.1093/brain/awt327 |
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author | Schulz, Alexander Kyselyova, Anna Baader, Stephan L. Jung, Marie Juliane Zoch, Ansgar Mautner, Victor-Felix Hagel, Christian Morrison, Helen |
author_facet | Schulz, Alexander Kyselyova, Anna Baader, Stephan L. Jung, Marie Juliane Zoch, Ansgar Mautner, Victor-Felix Hagel, Christian Morrison, Helen |
author_sort | Schulz, Alexander |
collection | PubMed |
description | Axonal surface proteins encompass a group of heterogeneous molecules, which exert a variety of different functions in the highly interdependent relationship between axons and Schwann cells. We recently revealed that the tumour suppressor protein merlin, mutated in the hereditary tumour syndrome neurofibromatosis type 2, impacts significantly on axon structure maintenance in the peripheral nervous system. We now report on a role of neuronal merlin in the regulation of the axonal surface protein neuregulin 1 important for modulating Schwann cell differentiation and myelination. Specifically, neuregulin 1 type III expression is reduced in sciatic nerve tissue of neuron-specific knockout animals as well as in biopsies from seven patients with neurofibromatosis type 2. In vitro experiments performed on both the P19 neuronal cell line and primary dorsal root ganglion cells demonstrate the influence of merlin on neuregulin 1 type III expression. Moreover, expression of ERBB2, a Schwann cell receptor for neuregulin 1 ligands is increased in nerve tissue of both neuron-specific merlin knockout animals and patients with neurofibromatosis type 2, demonstrating for the first time that axonal merlin indirectly regulates Schwann cell behaviour. Collectively, we have identified that neuronally expressed merlin can influence Schwann cell activity in a cell-extrinsic manner. |
format | Online Article Text |
id | pubmed-3914471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39144712014-02-05 Neuronal merlin influences ERBB2 receptor expression on Schwann cells through neuregulin 1 type III signalling Schulz, Alexander Kyselyova, Anna Baader, Stephan L. Jung, Marie Juliane Zoch, Ansgar Mautner, Victor-Felix Hagel, Christian Morrison, Helen Brain Original Articles Axonal surface proteins encompass a group of heterogeneous molecules, which exert a variety of different functions in the highly interdependent relationship between axons and Schwann cells. We recently revealed that the tumour suppressor protein merlin, mutated in the hereditary tumour syndrome neurofibromatosis type 2, impacts significantly on axon structure maintenance in the peripheral nervous system. We now report on a role of neuronal merlin in the regulation of the axonal surface protein neuregulin 1 important for modulating Schwann cell differentiation and myelination. Specifically, neuregulin 1 type III expression is reduced in sciatic nerve tissue of neuron-specific knockout animals as well as in biopsies from seven patients with neurofibromatosis type 2. In vitro experiments performed on both the P19 neuronal cell line and primary dorsal root ganglion cells demonstrate the influence of merlin on neuregulin 1 type III expression. Moreover, expression of ERBB2, a Schwann cell receptor for neuregulin 1 ligands is increased in nerve tissue of both neuron-specific merlin knockout animals and patients with neurofibromatosis type 2, demonstrating for the first time that axonal merlin indirectly regulates Schwann cell behaviour. Collectively, we have identified that neuronally expressed merlin can influence Schwann cell activity in a cell-extrinsic manner. Oxford University Press 2014-02 2013-12-05 /pmc/articles/PMC3914471/ /pubmed/24309211 http://dx.doi.org/10.1093/brain/awt327 Text en © The Author (2013). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Schulz, Alexander Kyselyova, Anna Baader, Stephan L. Jung, Marie Juliane Zoch, Ansgar Mautner, Victor-Felix Hagel, Christian Morrison, Helen Neuronal merlin influences ERBB2 receptor expression on Schwann cells through neuregulin 1 type III signalling |
title | Neuronal merlin influences ERBB2 receptor expression on Schwann cells through neuregulin 1 type III signalling |
title_full | Neuronal merlin influences ERBB2 receptor expression on Schwann cells through neuregulin 1 type III signalling |
title_fullStr | Neuronal merlin influences ERBB2 receptor expression on Schwann cells through neuregulin 1 type III signalling |
title_full_unstemmed | Neuronal merlin influences ERBB2 receptor expression on Schwann cells through neuregulin 1 type III signalling |
title_short | Neuronal merlin influences ERBB2 receptor expression on Schwann cells through neuregulin 1 type III signalling |
title_sort | neuronal merlin influences erbb2 receptor expression on schwann cells through neuregulin 1 type iii signalling |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914471/ https://www.ncbi.nlm.nih.gov/pubmed/24309211 http://dx.doi.org/10.1093/brain/awt327 |
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