Highly redundant neuropeptide volume co-transmission underlying episodic activation of the GnRH neuron dendron

The necessity and functional significance of neurotransmitter co-transmission remains unclear. The glutamatergic ‘KNDy’ neurons co-express kisspeptin, neurokinin B (NKB), and dynorphin and exhibit a highly stereotyped synchronized behavior that reads out to the gonadotropin-releasing hormone (GnRH)...

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Main Authors: Xinhuai Liu, Shel-Hwa Yeo, H James McQuillan, Michel K Herde, Sabine Hessler, Isaiah Cheong, Robert Porteous, Allan E Herbison
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-01-01
Series:eLife
Subjects:
NKB
Online Access:https://elifesciences.org/articles/62455
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spelling doaj-dd0834127aa343eea0d5fe477907a71f2021-05-05T22:42:08ZengeLife Sciences Publications LtdeLife2050-084X2021-01-011010.7554/eLife.62455Highly redundant neuropeptide volume co-transmission underlying episodic activation of the GnRH neuron dendronXinhuai Liu0Shel-Hwa Yeo1H James McQuillan2Michel K Herde3https://orcid.org/0000-0002-2324-2083Sabine Hessler4https://orcid.org/0000-0002-4177-4825Isaiah Cheong5Robert Porteous6Allan E Herbison7https://orcid.org/0000-0002-9615-3022Centre for Neuroendocrinology and Department of Physiology, University of Otago School of Biomedical Sciences, Dunedin, New ZealandCentre for Neuroendocrinology and Department of Physiology, University of Otago School of Biomedical Sciences, Dunedin, New Zealand; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United KingdomCentre for Neuroendocrinology and Department of Physiology, University of Otago School of Biomedical Sciences, Dunedin, New ZealandCentre for Neuroendocrinology and Department of Physiology, University of Otago School of Biomedical Sciences, Dunedin, New ZealandCentre for Neuroendocrinology and Department of Physiology, University of Otago School of Biomedical Sciences, Dunedin, New ZealandCentre for Neuroendocrinology and Department of Physiology, University of Otago School of Biomedical Sciences, Dunedin, New ZealandCentre for Neuroendocrinology and Department of Physiology, University of Otago School of Biomedical Sciences, Dunedin, New ZealandCentre for Neuroendocrinology and Department of Physiology, University of Otago School of Biomedical Sciences, Dunedin, New Zealand; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United KingdomThe necessity and functional significance of neurotransmitter co-transmission remains unclear. The glutamatergic ‘KNDy’ neurons co-express kisspeptin, neurokinin B (NKB), and dynorphin and exhibit a highly stereotyped synchronized behavior that reads out to the gonadotropin-releasing hormone (GnRH) neuron dendrons to drive episodic hormone secretion. Using expansion microscopy, we show that KNDy neurons make abundant close, non-synaptic appositions with the GnRH neuron dendron. Electrophysiology and confocal GCaMP6 imaging demonstrated that, despite all three neuropeptides being released from KNDy terminals, only kisspeptin was able to activate the GnRH neuron dendron. Mice with a selective deletion of kisspeptin from KNDy neurons failed to exhibit pulsatile hormone secretion but maintained synchronized episodic KNDy neuron behavior that is thought to depend on recurrent NKB and dynorphin transmission. This indicates that KNDy neurons drive episodic hormone secretion through highly redundant neuropeptide co-transmission orchestrated by differential post-synaptic neuropeptide receptor expression at the GnRH neuron dendron and KNDy neuron.https://elifesciences.org/articles/62455kisspeptinGnRHpulse generatorNKBDynorphinGCaMP
collection DOAJ
language English
format Article
sources DOAJ
author Xinhuai Liu
Shel-Hwa Yeo
H James McQuillan
Michel K Herde
Sabine Hessler
Isaiah Cheong
Robert Porteous
Allan E Herbison
spellingShingle Xinhuai Liu
Shel-Hwa Yeo
H James McQuillan
Michel K Herde
Sabine Hessler
Isaiah Cheong
Robert Porteous
Allan E Herbison
Highly redundant neuropeptide volume co-transmission underlying episodic activation of the GnRH neuron dendron
eLife
kisspeptin
GnRH
pulse generator
NKB
Dynorphin
GCaMP
author_facet Xinhuai Liu
Shel-Hwa Yeo
H James McQuillan
Michel K Herde
Sabine Hessler
Isaiah Cheong
Robert Porteous
Allan E Herbison
author_sort Xinhuai Liu
title Highly redundant neuropeptide volume co-transmission underlying episodic activation of the GnRH neuron dendron
title_short Highly redundant neuropeptide volume co-transmission underlying episodic activation of the GnRH neuron dendron
title_full Highly redundant neuropeptide volume co-transmission underlying episodic activation of the GnRH neuron dendron
title_fullStr Highly redundant neuropeptide volume co-transmission underlying episodic activation of the GnRH neuron dendron
title_full_unstemmed Highly redundant neuropeptide volume co-transmission underlying episodic activation of the GnRH neuron dendron
title_sort highly redundant neuropeptide volume co-transmission underlying episodic activation of the gnrh neuron dendron
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2021-01-01
description The necessity and functional significance of neurotransmitter co-transmission remains unclear. The glutamatergic ‘KNDy’ neurons co-express kisspeptin, neurokinin B (NKB), and dynorphin and exhibit a highly stereotyped synchronized behavior that reads out to the gonadotropin-releasing hormone (GnRH) neuron dendrons to drive episodic hormone secretion. Using expansion microscopy, we show that KNDy neurons make abundant close, non-synaptic appositions with the GnRH neuron dendron. Electrophysiology and confocal GCaMP6 imaging demonstrated that, despite all three neuropeptides being released from KNDy terminals, only kisspeptin was able to activate the GnRH neuron dendron. Mice with a selective deletion of kisspeptin from KNDy neurons failed to exhibit pulsatile hormone secretion but maintained synchronized episodic KNDy neuron behavior that is thought to depend on recurrent NKB and dynorphin transmission. This indicates that KNDy neurons drive episodic hormone secretion through highly redundant neuropeptide co-transmission orchestrated by differential post-synaptic neuropeptide receptor expression at the GnRH neuron dendron and KNDy neuron.
topic kisspeptin
GnRH
pulse generator
NKB
Dynorphin
GCaMP
url https://elifesciences.org/articles/62455
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