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Topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis
The sympathetic nervous system is crucial for controlling multiple cardiac functions. However, a comprehensive, detailed neuroanatomical map of the sympathetic innervation of the heart is unavailable. Here, we used a combination of state-of-the-art techniques, including flat-mount tissue processing,...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082215/ https://www.ncbi.nlm.nih.gov/pubmed/37029119 http://dx.doi.org/10.1038/s41598-023-27727-9 |
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author | Zhang, Yuanyuan Bizanti, Ariege Harden, Scott W. Chen, Jin Bendowski, Kohlton Hoover, Donald B. Gozal, David Shivkumar, Kalyanam Heal, Maci Tappan, Susan Cheng, Zixi Jack |
author_facet | Zhang, Yuanyuan Bizanti, Ariege Harden, Scott W. Chen, Jin Bendowski, Kohlton Hoover, Donald B. Gozal, David Shivkumar, Kalyanam Heal, Maci Tappan, Susan Cheng, Zixi Jack |
author_sort | Zhang, Yuanyuan |
collection | PubMed |
description | The sympathetic nervous system is crucial for controlling multiple cardiac functions. However, a comprehensive, detailed neuroanatomical map of the sympathetic innervation of the heart is unavailable. Here, we used a combination of state-of-the-art techniques, including flat-mount tissue processing, immunohistochemistry for tyrosine hydroxylase (TH, a sympathetic marker), confocal microscopy and Neurolucida 360 software to trace, digitize, and quantitatively map the topographical distribution of the sympathetic postganglionic innervation in whole atria of C57Bl/6 J mice. We found that (1) 4–5 major extrinsic TH-IR nerve bundles entered the atria at the superior vena cava, right atrium (RA), left precaval vein and the root of the pulmonary veins (PVs) in the left atrium (LA). Although these bundles projected to different areas of the atria, their projection fields partially overlapped. (2) TH-IR axon and terminal density varied considerably between different sites of the atria with the greatest density of innervation near the sinoatrial node region (P < 0.05, n = 6). (3) TH-IR axons also innervated blood vessels and adipocytes. (4) Many principal neurons in intrinsic cardiac ganglia and small intensely fluorescent cells were also strongly TH-IR. Our work provides a comprehensive topographical map of the catecholaminergic efferent axon morphology, innervation, and distribution in the whole atria at single cell/axon/varicosity scale that may be used in future studies to create a cardiac sympathetic-brain atlas. |
format | Online Article Text |
id | pubmed-10082215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100822152023-04-09 Topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis Zhang, Yuanyuan Bizanti, Ariege Harden, Scott W. Chen, Jin Bendowski, Kohlton Hoover, Donald B. Gozal, David Shivkumar, Kalyanam Heal, Maci Tappan, Susan Cheng, Zixi Jack Sci Rep Article The sympathetic nervous system is crucial for controlling multiple cardiac functions. However, a comprehensive, detailed neuroanatomical map of the sympathetic innervation of the heart is unavailable. Here, we used a combination of state-of-the-art techniques, including flat-mount tissue processing, immunohistochemistry for tyrosine hydroxylase (TH, a sympathetic marker), confocal microscopy and Neurolucida 360 software to trace, digitize, and quantitatively map the topographical distribution of the sympathetic postganglionic innervation in whole atria of C57Bl/6 J mice. We found that (1) 4–5 major extrinsic TH-IR nerve bundles entered the atria at the superior vena cava, right atrium (RA), left precaval vein and the root of the pulmonary veins (PVs) in the left atrium (LA). Although these bundles projected to different areas of the atria, their projection fields partially overlapped. (2) TH-IR axon and terminal density varied considerably between different sites of the atria with the greatest density of innervation near the sinoatrial node region (P < 0.05, n = 6). (3) TH-IR axons also innervated blood vessels and adipocytes. (4) Many principal neurons in intrinsic cardiac ganglia and small intensely fluorescent cells were also strongly TH-IR. Our work provides a comprehensive topographical map of the catecholaminergic efferent axon morphology, innervation, and distribution in the whole atria at single cell/axon/varicosity scale that may be used in future studies to create a cardiac sympathetic-brain atlas. Nature Publishing Group UK 2023-04-07 /pmc/articles/PMC10082215/ /pubmed/37029119 http://dx.doi.org/10.1038/s41598-023-27727-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhang, Yuanyuan Bizanti, Ariege Harden, Scott W. Chen, Jin Bendowski, Kohlton Hoover, Donald B. Gozal, David Shivkumar, Kalyanam Heal, Maci Tappan, Susan Cheng, Zixi Jack Topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis |
title | Topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis |
title_full | Topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis |
title_fullStr | Topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis |
title_full_unstemmed | Topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis |
title_short | Topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis |
title_sort | topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082215/ https://www.ncbi.nlm.nih.gov/pubmed/37029119 http://dx.doi.org/10.1038/s41598-023-27727-9 |
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