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Immunofluorescence characterization of innervation and nerve-immune cell interactions in mouse lymph nodes

The peripheral nervous system communicates specifically with the immune system via local interactions. These interactions include the “hardwiring” of sympathetic/ parasympathetic (efferent) and sensory nerves (afferent) to primary (e.g., thymus and bone marrow) and secondary (e.g., lymph node, splee...

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Autores principales: Hu, Dailun, Nicholls, Philip K., Claus, Melissa, Wu, Yongkang, Shi, Zhongli, Greene, Wayne K., Ma, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802453/
https://www.ncbi.nlm.nih.gov/pubmed/31631646
http://dx.doi.org/10.4081/ejh.2019.3059
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author Hu, Dailun
Nicholls, Philip K.
Claus, Melissa
Wu, Yongkang
Shi, Zhongli
Greene, Wayne K.
Ma, Bin
author_facet Hu, Dailun
Nicholls, Philip K.
Claus, Melissa
Wu, Yongkang
Shi, Zhongli
Greene, Wayne K.
Ma, Bin
author_sort Hu, Dailun
collection PubMed
description The peripheral nervous system communicates specifically with the immune system via local interactions. These interactions include the “hardwiring” of sympathetic/ parasympathetic (efferent) and sensory nerves (afferent) to primary (e.g., thymus and bone marrow) and secondary (e.g., lymph node, spleen, and gut-associated lymphoid tissue) lymphoid tissue/organs. To gain a better understanding of this bidirectional interaction/crosstalk between the two systems, we have investigated the distribution of nerve fibres and PNS-immune cell associations in situ in the mouse lymph node by using immunofluorescent staining and confocal microscopy/ three-dimensional reconstruction. Our results demonstrate: i) the presence of extensive nerve fibres in all compartments (including B cell follicles) in the mouse lymph node; ii) close contacts/ associations of nerve fibres with blood vessels (including high endothelial venules) and lymphatic vessels/sinuses; iii) close contacts/associations of nerve fibres with various subsets of dendritic cells (e.g., B220(+)CD11c(+), CD4(+)CD11c(+), CD8a(+) CD11c(+), and Mac1(+)CD11c(+)), Mac1(+) macrophages, and B/T lymphocytes. Our novel findings concerning the innervation and nerve-immune cell interactions inside the mouse lymph node should greatly facilitate our understanding of the effects that the peripheral nervous system has on cellular- and humoral-mediated immune responses or vice versa in health and disease.
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spelling pubmed-68024532019-11-07 Immunofluorescence characterization of innervation and nerve-immune cell interactions in mouse lymph nodes Hu, Dailun Nicholls, Philip K. Claus, Melissa Wu, Yongkang Shi, Zhongli Greene, Wayne K. Ma, Bin Eur J Histochem Original Paper The peripheral nervous system communicates specifically with the immune system via local interactions. These interactions include the “hardwiring” of sympathetic/ parasympathetic (efferent) and sensory nerves (afferent) to primary (e.g., thymus and bone marrow) and secondary (e.g., lymph node, spleen, and gut-associated lymphoid tissue) lymphoid tissue/organs. To gain a better understanding of this bidirectional interaction/crosstalk between the two systems, we have investigated the distribution of nerve fibres and PNS-immune cell associations in situ in the mouse lymph node by using immunofluorescent staining and confocal microscopy/ three-dimensional reconstruction. Our results demonstrate: i) the presence of extensive nerve fibres in all compartments (including B cell follicles) in the mouse lymph node; ii) close contacts/ associations of nerve fibres with blood vessels (including high endothelial venules) and lymphatic vessels/sinuses; iii) close contacts/associations of nerve fibres with various subsets of dendritic cells (e.g., B220(+)CD11c(+), CD4(+)CD11c(+), CD8a(+) CD11c(+), and Mac1(+)CD11c(+)), Mac1(+) macrophages, and B/T lymphocytes. Our novel findings concerning the innervation and nerve-immune cell interactions inside the mouse lymph node should greatly facilitate our understanding of the effects that the peripheral nervous system has on cellular- and humoral-mediated immune responses or vice versa in health and disease. PAGEPress Publications, Pavia, Italy 2019-10-18 /pmc/articles/PMC6802453/ /pubmed/31631646 http://dx.doi.org/10.4081/ejh.2019.3059 Text en ©Copyright: the Author(s), 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Hu, Dailun
Nicholls, Philip K.
Claus, Melissa
Wu, Yongkang
Shi, Zhongli
Greene, Wayne K.
Ma, Bin
Immunofluorescence characterization of innervation and nerve-immune cell interactions in mouse lymph nodes
title Immunofluorescence characterization of innervation and nerve-immune cell interactions in mouse lymph nodes
title_full Immunofluorescence characterization of innervation and nerve-immune cell interactions in mouse lymph nodes
title_fullStr Immunofluorescence characterization of innervation and nerve-immune cell interactions in mouse lymph nodes
title_full_unstemmed Immunofluorescence characterization of innervation and nerve-immune cell interactions in mouse lymph nodes
title_short Immunofluorescence characterization of innervation and nerve-immune cell interactions in mouse lymph nodes
title_sort immunofluorescence characterization of innervation and nerve-immune cell interactions in mouse lymph nodes
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802453/
https://www.ncbi.nlm.nih.gov/pubmed/31631646
http://dx.doi.org/10.4081/ejh.2019.3059
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