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Distribution of α7 Nicotinic Acetylcholine Receptor Subunit mRNA in the Developing Mouse

Homomeric α7 nicotinic acetylcholine receptors (nAChRs) are abundantly expressed in the central and peripheral nervous system (CNS and PNS, respectively), and spinal cord. In addition, expression and functional responses have been reported in non-neuronal tissue. In the nervous system, α7 nAChR subu...

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Autores principales: Broide, Ron S., Winzer-Serhan, Ursula H., Chen, Yling, Leslie, Frances M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691102/
https://www.ncbi.nlm.nih.gov/pubmed/31447654
http://dx.doi.org/10.3389/fnana.2019.00076
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author Broide, Ron S.
Winzer-Serhan, Ursula H.
Chen, Yling
Leslie, Frances M.
author_facet Broide, Ron S.
Winzer-Serhan, Ursula H.
Chen, Yling
Leslie, Frances M.
author_sort Broide, Ron S.
collection PubMed
description Homomeric α7 nicotinic acetylcholine receptors (nAChRs) are abundantly expressed in the central and peripheral nervous system (CNS and PNS, respectively), and spinal cord. In addition, expression and functional responses have been reported in non-neuronal tissue. In the nervous system, α7 nAChR subunit expression appears early during embryonic development and is often transiently upregulated, but little is known about their prenatal expression outside of the nervous system. For understanding potential short-term and long-term effects of gestational nicotine exposure, it is important to know the temporal and spatial expression of α7 nAChRs throughout the body. To that end, we studied the expression of α7 nAChR subunit mRNA using highly sensitive isotopic in situ hybridization in embryonic and neonatal whole-body mouse sections starting at gestational day 13. The results revealed expression of α7 mRNA as early as embryonic day 13 in the PNS, including dorsal root ganglia, parasympathetic and sympathetic ganglia, with the strongest expression in the superior cervical ganglion, and low to moderate levels were detected in brain and spinal cord, respectively, which rapidly increased in intensity with embryonic age. In addition, robust α7 mRNA expression was detected in the adrenal medulla, and low to moderate expression in selected peripheral tissues during embryonic development, potentially related to cells derived from the neural crest. Little or no mRNA expression was detected in thymus or spleen, sites of immune cell maturation. The results suggest that prenatal nicotine exposure could potentially affect the nervous system with limited effects in non-neural tissues.
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spelling pubmed-66911022019-08-23 Distribution of α7 Nicotinic Acetylcholine Receptor Subunit mRNA in the Developing Mouse Broide, Ron S. Winzer-Serhan, Ursula H. Chen, Yling Leslie, Frances M. Front Neuroanat Neuroanatomy Homomeric α7 nicotinic acetylcholine receptors (nAChRs) are abundantly expressed in the central and peripheral nervous system (CNS and PNS, respectively), and spinal cord. In addition, expression and functional responses have been reported in non-neuronal tissue. In the nervous system, α7 nAChR subunit expression appears early during embryonic development and is often transiently upregulated, but little is known about their prenatal expression outside of the nervous system. For understanding potential short-term and long-term effects of gestational nicotine exposure, it is important to know the temporal and spatial expression of α7 nAChRs throughout the body. To that end, we studied the expression of α7 nAChR subunit mRNA using highly sensitive isotopic in situ hybridization in embryonic and neonatal whole-body mouse sections starting at gestational day 13. The results revealed expression of α7 mRNA as early as embryonic day 13 in the PNS, including dorsal root ganglia, parasympathetic and sympathetic ganglia, with the strongest expression in the superior cervical ganglion, and low to moderate levels were detected in brain and spinal cord, respectively, which rapidly increased in intensity with embryonic age. In addition, robust α7 mRNA expression was detected in the adrenal medulla, and low to moderate expression in selected peripheral tissues during embryonic development, potentially related to cells derived from the neural crest. Little or no mRNA expression was detected in thymus or spleen, sites of immune cell maturation. The results suggest that prenatal nicotine exposure could potentially affect the nervous system with limited effects in non-neural tissues. Frontiers Media S.A. 2019-08-06 /pmc/articles/PMC6691102/ /pubmed/31447654 http://dx.doi.org/10.3389/fnana.2019.00076 Text en Copyright © 2019 Broide, Winzer-Serhan, Chen and Leslie. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroanatomy
Broide, Ron S.
Winzer-Serhan, Ursula H.
Chen, Yling
Leslie, Frances M.
Distribution of α7 Nicotinic Acetylcholine Receptor Subunit mRNA in the Developing Mouse
title Distribution of α7 Nicotinic Acetylcholine Receptor Subunit mRNA in the Developing Mouse
title_full Distribution of α7 Nicotinic Acetylcholine Receptor Subunit mRNA in the Developing Mouse
title_fullStr Distribution of α7 Nicotinic Acetylcholine Receptor Subunit mRNA in the Developing Mouse
title_full_unstemmed Distribution of α7 Nicotinic Acetylcholine Receptor Subunit mRNA in the Developing Mouse
title_short Distribution of α7 Nicotinic Acetylcholine Receptor Subunit mRNA in the Developing Mouse
title_sort distribution of α7 nicotinic acetylcholine receptor subunit mrna in the developing mouse
topic Neuroanatomy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691102/
https://www.ncbi.nlm.nih.gov/pubmed/31447654
http://dx.doi.org/10.3389/fnana.2019.00076
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