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Maturation of suprathreshold auditory nerve activity involves cochlear CGRP–receptor complex formation
In adult animals, the neuropeptide calcitonin gene‐related peptide (CGRP) is contained in cochlear efferent fibers projecting out to the cochlea, and contributes to increased suprathreshold sound‐evoked activity in the adult auditory nerve. Similarly, CGRP applied to the lateral‐line organ (hair cel...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962074/ https://www.ncbi.nlm.nih.gov/pubmed/27440744 http://dx.doi.org/10.14814/phy2.12869 |
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author | Dickerson, Ian M. Bussey‐Gaborski, Rhiannon Holt, Joseph C. Jordan, Paivi M. Luebke, Anne E. |
author_facet | Dickerson, Ian M. Bussey‐Gaborski, Rhiannon Holt, Joseph C. Jordan, Paivi M. Luebke, Anne E. |
author_sort | Dickerson, Ian M. |
collection | PubMed |
description | In adult animals, the neuropeptide calcitonin gene‐related peptide (CGRP) is contained in cochlear efferent fibers projecting out to the cochlea, and contributes to increased suprathreshold sound‐evoked activity in the adult auditory nerve. Similarly, CGRP applied to the lateral‐line organ (hair cell organ) increases afferent nerve activity in adult frogs (post‐metamorphic day 30), yet this increase is developmentally delayed from post‐metamorphic day 4–30. In this study, we discovered that there was also a developmental delay in increased suprathreshold sound‐evoked activity auditory nerve between juvenile and adult mice similar to what had been observed previously in frog. Moreover, juvenile mice with a targeted deletion of the α CGRP gene [CGRP null (−/−)] did not show a similar developmental increase in nerve activity, suggesting CGRP signaling is involved. This developmental delay is not due to a delay in CGRP expression, but instead is due to a delay in receptor formation. We observed that the increase in sound‐evoked nerve activity is correlated with increased formation of cochlear CGRP receptors, which require three complexed proteins (CLR, RAMP1, RCP) to be functional. CGRP receptor formation in the cochlea was incomplete at 1 month of age (juvenile), but complete by 3 months (adult), which corresponded to the onset of suprathreshold enhancement of sound‐evoked activity in wild‐type animals. Taken together, these data support a model for cochlear function that is enhanced by maturation of CGRP receptor complexes. |
format | Online Article Text |
id | pubmed-4962074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49620742016-08-05 Maturation of suprathreshold auditory nerve activity involves cochlear CGRP–receptor complex formation Dickerson, Ian M. Bussey‐Gaborski, Rhiannon Holt, Joseph C. Jordan, Paivi M. Luebke, Anne E. Physiol Rep Original Research In adult animals, the neuropeptide calcitonin gene‐related peptide (CGRP) is contained in cochlear efferent fibers projecting out to the cochlea, and contributes to increased suprathreshold sound‐evoked activity in the adult auditory nerve. Similarly, CGRP applied to the lateral‐line organ (hair cell organ) increases afferent nerve activity in adult frogs (post‐metamorphic day 30), yet this increase is developmentally delayed from post‐metamorphic day 4–30. In this study, we discovered that there was also a developmental delay in increased suprathreshold sound‐evoked activity auditory nerve between juvenile and adult mice similar to what had been observed previously in frog. Moreover, juvenile mice with a targeted deletion of the α CGRP gene [CGRP null (−/−)] did not show a similar developmental increase in nerve activity, suggesting CGRP signaling is involved. This developmental delay is not due to a delay in CGRP expression, but instead is due to a delay in receptor formation. We observed that the increase in sound‐evoked nerve activity is correlated with increased formation of cochlear CGRP receptors, which require three complexed proteins (CLR, RAMP1, RCP) to be functional. CGRP receptor formation in the cochlea was incomplete at 1 month of age (juvenile), but complete by 3 months (adult), which corresponded to the onset of suprathreshold enhancement of sound‐evoked activity in wild‐type animals. Taken together, these data support a model for cochlear function that is enhanced by maturation of CGRP receptor complexes. John Wiley and Sons Inc. 2016-07-20 /pmc/articles/PMC4962074/ /pubmed/27440744 http://dx.doi.org/10.14814/phy2.12869 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Dickerson, Ian M. Bussey‐Gaborski, Rhiannon Holt, Joseph C. Jordan, Paivi M. Luebke, Anne E. Maturation of suprathreshold auditory nerve activity involves cochlear CGRP–receptor complex formation |
title | Maturation of suprathreshold auditory nerve activity involves cochlear CGRP–receptor complex formation |
title_full | Maturation of suprathreshold auditory nerve activity involves cochlear CGRP–receptor complex formation |
title_fullStr | Maturation of suprathreshold auditory nerve activity involves cochlear CGRP–receptor complex formation |
title_full_unstemmed | Maturation of suprathreshold auditory nerve activity involves cochlear CGRP–receptor complex formation |
title_short | Maturation of suprathreshold auditory nerve activity involves cochlear CGRP–receptor complex formation |
title_sort | maturation of suprathreshold auditory nerve activity involves cochlear cgrp–receptor complex formation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962074/ https://www.ncbi.nlm.nih.gov/pubmed/27440744 http://dx.doi.org/10.14814/phy2.12869 |
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