Cargando…

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,...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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
_version_ 1785021272971804672
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
work_keys_str_mv AT zhangyuanyuan topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT bizantiariege topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT hardenscottw topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT chenjin topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT bendowskikohlton topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT hooverdonaldb topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT gozaldavid topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT shivkumarkalyanam topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT healmaci topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT tappansusan topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis
AT chengzixijack topographicalmappingofcatecholaminergicaxoninnervationintheflatmountsofthemouseatriaaquantitativeanalysis