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Ultrastructural mapping of salivary gland innervation in the tick Ixodes ricinus

The salivary gland of hard ticks is a highly innervated tissue where multiple intertwined axonal projections enter each individual acini. In the present study, we investigated the ultrastructural architecture of axonal projections within granular salivary gland type II and III acini of Ixodes ricinu...

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Autores principales: Vancová, Marie, Bílý, Tomáš, Nebesářová, Jana, Grubhoffer, Libor, Bonnet, Sarah, Park, Yoonseong, Šimo, Ladislav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497691/
https://www.ncbi.nlm.nih.gov/pubmed/31048723
http://dx.doi.org/10.1038/s41598-019-43284-6
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author Vancová, Marie
Bílý, Tomáš
Nebesářová, Jana
Grubhoffer, Libor
Bonnet, Sarah
Park, Yoonseong
Šimo, Ladislav
author_facet Vancová, Marie
Bílý, Tomáš
Nebesářová, Jana
Grubhoffer, Libor
Bonnet, Sarah
Park, Yoonseong
Šimo, Ladislav
author_sort Vancová, Marie
collection PubMed
description The salivary gland of hard ticks is a highly innervated tissue where multiple intertwined axonal projections enter each individual acini. In the present study, we investigated the ultrastructural architecture of axonal projections within granular salivary gland type II and III acini of Ixodes ricinus female. Using immunogold labeling, we specifically examined the associations of SIFamide neuropeptide, SIFamide receptor (SIFa_R), neuropeptide pigment dispersing factor (PDF), and the invertebrate-specific D1-like dopamine receptor (InvD1L), with acinar cells. In both acini types, SIFamide-positive axons were found to be in direct contact with either basal epithelial cells or a single adlumenal myoepithelial cell in close proximity to the either the acinar duct or its valve, respectively. Accordingly, SIFa_R staining correlated with SIFamide-positive axons in both basal epithelial and myoepithelial cells. Immunoreactivity for both InvD1L and PDF (type II acini exclusively) revealed positive axons radiating along the acinar lumen. These axons were primarily enclosed by the adlumenal myoepithelial cell plasma membrane and interstitial projections of ablumenal epithelial cells. Our study has revealed the detailed ultrastructure of I. ricinus salivary glands, and provides a solid baseline for a comprehensive understanding of the cell-axon interactions and their functions in this essential tick organ.
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spelling pubmed-64976912019-05-17 Ultrastructural mapping of salivary gland innervation in the tick Ixodes ricinus Vancová, Marie Bílý, Tomáš Nebesářová, Jana Grubhoffer, Libor Bonnet, Sarah Park, Yoonseong Šimo, Ladislav Sci Rep Article The salivary gland of hard ticks is a highly innervated tissue where multiple intertwined axonal projections enter each individual acini. In the present study, we investigated the ultrastructural architecture of axonal projections within granular salivary gland type II and III acini of Ixodes ricinus female. Using immunogold labeling, we specifically examined the associations of SIFamide neuropeptide, SIFamide receptor (SIFa_R), neuropeptide pigment dispersing factor (PDF), and the invertebrate-specific D1-like dopamine receptor (InvD1L), with acinar cells. In both acini types, SIFamide-positive axons were found to be in direct contact with either basal epithelial cells or a single adlumenal myoepithelial cell in close proximity to the either the acinar duct or its valve, respectively. Accordingly, SIFa_R staining correlated with SIFamide-positive axons in both basal epithelial and myoepithelial cells. Immunoreactivity for both InvD1L and PDF (type II acini exclusively) revealed positive axons radiating along the acinar lumen. These axons were primarily enclosed by the adlumenal myoepithelial cell plasma membrane and interstitial projections of ablumenal epithelial cells. Our study has revealed the detailed ultrastructure of I. ricinus salivary glands, and provides a solid baseline for a comprehensive understanding of the cell-axon interactions and their functions in this essential tick organ. Nature Publishing Group UK 2019-05-02 /pmc/articles/PMC6497691/ /pubmed/31048723 http://dx.doi.org/10.1038/s41598-019-43284-6 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Vancová, Marie
Bílý, Tomáš
Nebesářová, Jana
Grubhoffer, Libor
Bonnet, Sarah
Park, Yoonseong
Šimo, Ladislav
Ultrastructural mapping of salivary gland innervation in the tick Ixodes ricinus
title Ultrastructural mapping of salivary gland innervation in the tick Ixodes ricinus
title_full Ultrastructural mapping of salivary gland innervation in the tick Ixodes ricinus
title_fullStr Ultrastructural mapping of salivary gland innervation in the tick Ixodes ricinus
title_full_unstemmed Ultrastructural mapping of salivary gland innervation in the tick Ixodes ricinus
title_short Ultrastructural mapping of salivary gland innervation in the tick Ixodes ricinus
title_sort ultrastructural mapping of salivary gland innervation in the tick ixodes ricinus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497691/
https://www.ncbi.nlm.nih.gov/pubmed/31048723
http://dx.doi.org/10.1038/s41598-019-43284-6
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