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Glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles
Our aim in the present study was to determine whether a glutamatergic modulatory system involving synaptic-like vesicles (SLVs) is present in the lanceolate ending of the mouse and rat hair follicle and, if so, to assess its similarity to that of the rat muscle spindle annulospiral ending we have de...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Science Inc
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678041/ https://www.ncbi.nlm.nih.gov/pubmed/23440964 http://dx.doi.org/10.1113/jphysiol.2012.243659 |
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author | Banks, Robert W Cahusac, Peter M B Graca, Anna Kain, Nakul Shenton, Fiona Singh, Paramjeet Njå, Arild Simon, Anna Watson, Sonia Slater, Clarke R Bewick, Guy S |
author_facet | Banks, Robert W Cahusac, Peter M B Graca, Anna Kain, Nakul Shenton, Fiona Singh, Paramjeet Njå, Arild Simon, Anna Watson, Sonia Slater, Clarke R Bewick, Guy S |
author_sort | Banks, Robert W |
collection | PubMed |
description | Our aim in the present study was to determine whether a glutamatergic modulatory system involving synaptic-like vesicles (SLVs) is present in the lanceolate ending of the mouse and rat hair follicle and, if so, to assess its similarity to that of the rat muscle spindle annulospiral ending we have described previously. Both types of endings are formed by the peripheral sensory terminals of primary mechanosensory dorsal root ganglion cells, so the presence of such a system in the lanceolate ending would provide support for our hypothesis that it is a general property of fundamental importance to the regulation of the responsiveness of the broad class of primary mechanosensory endings. We show not only that an SLV-based system is present in lanceolate endings, but also that there are clear parallels between its operation in the two types of mechanosensory endings. In particular, we demonstrate that, as in the muscle spindle: (i) FM1-43 labels the sensory terminals of the lanceolate ending, rather than the closely associated accessory (glial) cells; (ii) the dye enters and leaves the terminals primarily by SLV recycling; (iii) the dye does not block the electrical response to mechanical stimulation, in contrast to its effect on the hair cell and dorsal root ganglion cells in culture; (iv) SLV recycling is Ca(2+) sensitive; and (v) the sensory terminals are enriched in glutamate. Thus, in the lanceolate sensory ending SLV recycling is itself regulated, at least in part, by glutamate acting through a phospholipase D-coupled metabotropic glutamate receptor. |
format | Online Article Text |
id | pubmed-3678041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Science Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-36780412013-08-05 Glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles Banks, Robert W Cahusac, Peter M B Graca, Anna Kain, Nakul Shenton, Fiona Singh, Paramjeet Njå, Arild Simon, Anna Watson, Sonia Slater, Clarke R Bewick, Guy S J Physiol Neuroscience: Cellular/Molecular Our aim in the present study was to determine whether a glutamatergic modulatory system involving synaptic-like vesicles (SLVs) is present in the lanceolate ending of the mouse and rat hair follicle and, if so, to assess its similarity to that of the rat muscle spindle annulospiral ending we have described previously. Both types of endings are formed by the peripheral sensory terminals of primary mechanosensory dorsal root ganglion cells, so the presence of such a system in the lanceolate ending would provide support for our hypothesis that it is a general property of fundamental importance to the regulation of the responsiveness of the broad class of primary mechanosensory endings. We show not only that an SLV-based system is present in lanceolate endings, but also that there are clear parallels between its operation in the two types of mechanosensory endings. In particular, we demonstrate that, as in the muscle spindle: (i) FM1-43 labels the sensory terminals of the lanceolate ending, rather than the closely associated accessory (glial) cells; (ii) the dye enters and leaves the terminals primarily by SLV recycling; (iii) the dye does not block the electrical response to mechanical stimulation, in contrast to its effect on the hair cell and dorsal root ganglion cells in culture; (iv) SLV recycling is Ca(2+) sensitive; and (v) the sensory terminals are enriched in glutamate. Thus, in the lanceolate sensory ending SLV recycling is itself regulated, at least in part, by glutamate acting through a phospholipase D-coupled metabotropic glutamate receptor. Blackwell Science Inc 2013-05-15 2013-02-25 /pmc/articles/PMC3678041/ /pubmed/23440964 http://dx.doi.org/10.1113/jphysiol.2012.243659 Text en © 2013 The Authors. The Journal of Physiology © 2013 The Physiological Society |
spellingShingle | Neuroscience: Cellular/Molecular Banks, Robert W Cahusac, Peter M B Graca, Anna Kain, Nakul Shenton, Fiona Singh, Paramjeet Njå, Arild Simon, Anna Watson, Sonia Slater, Clarke R Bewick, Guy S Glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles |
title | Glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles |
title_full | Glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles |
title_fullStr | Glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles |
title_full_unstemmed | Glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles |
title_short | Glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles |
title_sort | glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles |
topic | Neuroscience: Cellular/Molecular |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678041/ https://www.ncbi.nlm.nih.gov/pubmed/23440964 http://dx.doi.org/10.1113/jphysiol.2012.243659 |
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