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Neuron cilia constrain glial regulators to microdomains around distal neurons

Each glia interacts with multiple neurons, but the fundamental logic of whether it interacts with all equally remains unclear. We find that a single sense-organ glia modulates different contacting neurons distinctly. To do so, it partitions regulatory cues into molecular microdomains at specific neu...

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Autores principales: Ray, Sneha, Gurung, Pralaksha, Manning, R. Sean, Kravchuk, Alexandra, Singhvi, Aakanksha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055228/
https://www.ncbi.nlm.nih.gov/pubmed/36993507
http://dx.doi.org/10.1101/2023.03.18.533255
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author Ray, Sneha
Gurung, Pralaksha
Manning, R. Sean
Kravchuk, Alexandra
Singhvi, Aakanksha
author_facet Ray, Sneha
Gurung, Pralaksha
Manning, R. Sean
Kravchuk, Alexandra
Singhvi, Aakanksha
author_sort Ray, Sneha
collection PubMed
description Each glia interacts with multiple neurons, but the fundamental logic of whether it interacts with all equally remains unclear. We find that a single sense-organ glia modulates different contacting neurons distinctly. To do so, it partitions regulatory cues into molecular microdomains at specific neuron contact-sites, at its delimited apical membrane. For one glial cue, K/Cl transporter KCC-3, microdomain-localization occurs through a two-step, neuron-dependent process. First, KCC-3 shuttles to glial apical membranes. Second, some contacting neuron cilia repel it, rendering it microdomain-localized around one distal neuron-ending. KCC-3 localization tracks animal aging, and while apical localization is sufficient for contacting neuron function, microdomain-restriction is required for distal neuron properties. Finally, we find the glia regulates its microdomains largely independently. Together, this uncovers that glia modulate cross-modal sensor processing by compartmentalizing regulatory cues into microdomains. Glia across species contact multiple neurons and localize disease-relevant cues like KCC-3. Thus, analogous compartmentalization may broadly drive how glia regulate information processing across neural circuits.
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spelling pubmed-100552282023-03-30 Neuron cilia constrain glial regulators to microdomains around distal neurons Ray, Sneha Gurung, Pralaksha Manning, R. Sean Kravchuk, Alexandra Singhvi, Aakanksha bioRxiv Article Each glia interacts with multiple neurons, but the fundamental logic of whether it interacts with all equally remains unclear. We find that a single sense-organ glia modulates different contacting neurons distinctly. To do so, it partitions regulatory cues into molecular microdomains at specific neuron contact-sites, at its delimited apical membrane. For one glial cue, K/Cl transporter KCC-3, microdomain-localization occurs through a two-step, neuron-dependent process. First, KCC-3 shuttles to glial apical membranes. Second, some contacting neuron cilia repel it, rendering it microdomain-localized around one distal neuron-ending. KCC-3 localization tracks animal aging, and while apical localization is sufficient for contacting neuron function, microdomain-restriction is required for distal neuron properties. Finally, we find the glia regulates its microdomains largely independently. Together, this uncovers that glia modulate cross-modal sensor processing by compartmentalizing regulatory cues into microdomains. Glia across species contact multiple neurons and localize disease-relevant cues like KCC-3. Thus, analogous compartmentalization may broadly drive how glia regulate information processing across neural circuits. Cold Spring Harbor Laboratory 2023-03-18 /pmc/articles/PMC10055228/ /pubmed/36993507 http://dx.doi.org/10.1101/2023.03.18.533255 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Ray, Sneha
Gurung, Pralaksha
Manning, R. Sean
Kravchuk, Alexandra
Singhvi, Aakanksha
Neuron cilia constrain glial regulators to microdomains around distal neurons
title Neuron cilia constrain glial regulators to microdomains around distal neurons
title_full Neuron cilia constrain glial regulators to microdomains around distal neurons
title_fullStr Neuron cilia constrain glial regulators to microdomains around distal neurons
title_full_unstemmed Neuron cilia constrain glial regulators to microdomains around distal neurons
title_short Neuron cilia constrain glial regulators to microdomains around distal neurons
title_sort neuron cilia constrain glial regulators to microdomains around distal neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055228/
https://www.ncbi.nlm.nih.gov/pubmed/36993507
http://dx.doi.org/10.1101/2023.03.18.533255
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