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Nanotube‐like processes facilitate material transfer between photoreceptors

Neuronal communication is typically mediated via synapses and gap junctions. New forms of intercellular communication, including nanotubes (NTs) and extracellular vesicles (EVs), have been described for non‐neuronal cells, but their role in neuronal communication is not known. Recently, transfer of...

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Autores principales: Kalargyrou, Aikaterini A, Basche, Mark, Hare, Aura, West, Emma L, Smith, Alexander J, Ali, Robin R, Pearson, Rachael A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567251/
https://www.ncbi.nlm.nih.gov/pubmed/34494703
http://dx.doi.org/10.15252/embr.202153732
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author Kalargyrou, Aikaterini A
Basche, Mark
Hare, Aura
West, Emma L
Smith, Alexander J
Ali, Robin R
Pearson, Rachael A
author_facet Kalargyrou, Aikaterini A
Basche, Mark
Hare, Aura
West, Emma L
Smith, Alexander J
Ali, Robin R
Pearson, Rachael A
author_sort Kalargyrou, Aikaterini A
collection PubMed
description Neuronal communication is typically mediated via synapses and gap junctions. New forms of intercellular communication, including nanotubes (NTs) and extracellular vesicles (EVs), have been described for non‐neuronal cells, but their role in neuronal communication is not known. Recently, transfer of cytoplasmic material between donor and host neurons (“material transfer”) was shown to occur after photoreceptor transplantation. The cellular mechanism(s) underlying this surprising finding are unknown. Here, using transplantation, primary neuronal cultures and the generation of chimeric retinae, we show for the first time that mammalian photoreceptor neurons can form open‐end NT‐like processes. These processes permit the transfer of cytoplasmic and membrane‐bound molecules in culture and after transplantation and can mediate gain‐of‐function in the acceptor cells. Rarely, organelles were also observed to transfer. Strikingly, use of chimeric retinae revealed that material transfer can occur between photoreceptors in the intact adult retina. Conversely, while photoreceptors are capable of releasing EVs, at least in culture, these are taken up by glia and not by retinal neurons. Our findings provide the first evidence of functional NT‐like processes forming between sensory neurons in culture and in vivo.
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spelling pubmed-85672512021-11-12 Nanotube‐like processes facilitate material transfer between photoreceptors Kalargyrou, Aikaterini A Basche, Mark Hare, Aura West, Emma L Smith, Alexander J Ali, Robin R Pearson, Rachael A EMBO Rep Articles Neuronal communication is typically mediated via synapses and gap junctions. New forms of intercellular communication, including nanotubes (NTs) and extracellular vesicles (EVs), have been described for non‐neuronal cells, but their role in neuronal communication is not known. Recently, transfer of cytoplasmic material between donor and host neurons (“material transfer”) was shown to occur after photoreceptor transplantation. The cellular mechanism(s) underlying this surprising finding are unknown. Here, using transplantation, primary neuronal cultures and the generation of chimeric retinae, we show for the first time that mammalian photoreceptor neurons can form open‐end NT‐like processes. These processes permit the transfer of cytoplasmic and membrane‐bound molecules in culture and after transplantation and can mediate gain‐of‐function in the acceptor cells. Rarely, organelles were also observed to transfer. Strikingly, use of chimeric retinae revealed that material transfer can occur between photoreceptors in the intact adult retina. Conversely, while photoreceptors are capable of releasing EVs, at least in culture, these are taken up by glia and not by retinal neurons. Our findings provide the first evidence of functional NT‐like processes forming between sensory neurons in culture and in vivo. John Wiley and Sons Inc. 2021-09-08 2021-11-04 /pmc/articles/PMC8567251/ /pubmed/34494703 http://dx.doi.org/10.15252/embr.202153732 Text en © 2021 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Kalargyrou, Aikaterini A
Basche, Mark
Hare, Aura
West, Emma L
Smith, Alexander J
Ali, Robin R
Pearson, Rachael A
Nanotube‐like processes facilitate material transfer between photoreceptors
title Nanotube‐like processes facilitate material transfer between photoreceptors
title_full Nanotube‐like processes facilitate material transfer between photoreceptors
title_fullStr Nanotube‐like processes facilitate material transfer between photoreceptors
title_full_unstemmed Nanotube‐like processes facilitate material transfer between photoreceptors
title_short Nanotube‐like processes facilitate material transfer between photoreceptors
title_sort nanotube‐like processes facilitate material transfer between photoreceptors
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567251/
https://www.ncbi.nlm.nih.gov/pubmed/34494703
http://dx.doi.org/10.15252/embr.202153732
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