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Airway branching has conserved needs for local parasympathetic innervation but not neurotransmission

BACKGROUND: Parasympathetic signaling has been inferred to regulate epithelial branching as well as organ regeneration and tumor development. However, the relative contribution of local nerve contact versus secreted signals remains unclear. Here, we show a conserved (vertebrates to invertebrates) re...

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Autores principales: Bower, Danielle V, Lee, Hyung-Kook, Lansford, Rusty, Zinn, Kai, Warburton, David, Fraser, Scott E, Jesudason, Edwin C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255442/
https://www.ncbi.nlm.nih.gov/pubmed/25385196
http://dx.doi.org/10.1186/s12915-014-0092-2
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author Bower, Danielle V
Lee, Hyung-Kook
Lansford, Rusty
Zinn, Kai
Warburton, David
Fraser, Scott E
Jesudason, Edwin C
author_facet Bower, Danielle V
Lee, Hyung-Kook
Lansford, Rusty
Zinn, Kai
Warburton, David
Fraser, Scott E
Jesudason, Edwin C
author_sort Bower, Danielle V
collection PubMed
description BACKGROUND: Parasympathetic signaling has been inferred to regulate epithelial branching as well as organ regeneration and tumor development. However, the relative contribution of local nerve contact versus secreted signals remains unclear. Here, we show a conserved (vertebrates to invertebrates) requirement for intact local nerves in airway branching, persisting even when cholinergic neurotransmission is blocked. RESULTS: In the vertebrate lung, deleting enhanced green fluorescent protein (eGFP)-labeled intrinsic neurons using a two-photon laser leaves adjacent cells intact, but abolishes branching. Branching is unaffected by similar laser power delivered to the immediately adjacent non-neural mesodermal tissue, by blocking cholinergic receptors or by blocking synaptic transmission with botulinum toxin A. Because adjacent vasculature and epithelial proliferation also contribute to branching in the vertebrate lung, the direct dependence on nerves for airway branching was tested by deleting neurons in Drosophila embryos. A specific deletion of neurons in the Drosophila embryo by driving cell-autonomous RicinA under the pan-neuronal elav enhancer perturbed Drosophila airway development. This system confirmed that even in the absence of a vasculature or epithelial proliferation, airway branching is still disrupted by neural lesioning. CONCLUSIONS: Together, this shows that airway morphogenesis requires local innervation in vertebrates and invertebrates, yet neurotransmission is dispensable. The need for innervation persists in the fly, wherein adjacent vasculature and epithelial proliferation are absent. Our novel, targeted laser ablation technique permitted the local function of parasympathetic innervation to be distinguished from neurotransmission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-014-0092-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-42554422014-12-05 Airway branching has conserved needs for local parasympathetic innervation but not neurotransmission Bower, Danielle V Lee, Hyung-Kook Lansford, Rusty Zinn, Kai Warburton, David Fraser, Scott E Jesudason, Edwin C BMC Biol Research Article BACKGROUND: Parasympathetic signaling has been inferred to regulate epithelial branching as well as organ regeneration and tumor development. However, the relative contribution of local nerve contact versus secreted signals remains unclear. Here, we show a conserved (vertebrates to invertebrates) requirement for intact local nerves in airway branching, persisting even when cholinergic neurotransmission is blocked. RESULTS: In the vertebrate lung, deleting enhanced green fluorescent protein (eGFP)-labeled intrinsic neurons using a two-photon laser leaves adjacent cells intact, but abolishes branching. Branching is unaffected by similar laser power delivered to the immediately adjacent non-neural mesodermal tissue, by blocking cholinergic receptors or by blocking synaptic transmission with botulinum toxin A. Because adjacent vasculature and epithelial proliferation also contribute to branching in the vertebrate lung, the direct dependence on nerves for airway branching was tested by deleting neurons in Drosophila embryos. A specific deletion of neurons in the Drosophila embryo by driving cell-autonomous RicinA under the pan-neuronal elav enhancer perturbed Drosophila airway development. This system confirmed that even in the absence of a vasculature or epithelial proliferation, airway branching is still disrupted by neural lesioning. CONCLUSIONS: Together, this shows that airway morphogenesis requires local innervation in vertebrates and invertebrates, yet neurotransmission is dispensable. The need for innervation persists in the fly, wherein adjacent vasculature and epithelial proliferation are absent. Our novel, targeted laser ablation technique permitted the local function of parasympathetic innervation to be distinguished from neurotransmission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-014-0092-2) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-11 /pmc/articles/PMC4255442/ /pubmed/25385196 http://dx.doi.org/10.1186/s12915-014-0092-2 Text en © Bower et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Bower, Danielle V
Lee, Hyung-Kook
Lansford, Rusty
Zinn, Kai
Warburton, David
Fraser, Scott E
Jesudason, Edwin C
Airway branching has conserved needs for local parasympathetic innervation but not neurotransmission
title Airway branching has conserved needs for local parasympathetic innervation but not neurotransmission
title_full Airway branching has conserved needs for local parasympathetic innervation but not neurotransmission
title_fullStr Airway branching has conserved needs for local parasympathetic innervation but not neurotransmission
title_full_unstemmed Airway branching has conserved needs for local parasympathetic innervation but not neurotransmission
title_short Airway branching has conserved needs for local parasympathetic innervation but not neurotransmission
title_sort airway branching has conserved needs for local parasympathetic innervation but not neurotransmission
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255442/
https://www.ncbi.nlm.nih.gov/pubmed/25385196
http://dx.doi.org/10.1186/s12915-014-0092-2
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