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Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus
When a neurotrophin binds at the presynapse, it sends survival signals all the way to the nucleus on signaling endosomes. These endosomes fuel their own journey with on-board glycolysis—but how is that journey initiated and maintained? Using microfluidic devices and mice, we find that the calcium re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730605/ https://www.ncbi.nlm.nih.gov/pubmed/34985962 http://dx.doi.org/10.1126/sciadv.abj8812 |
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author | Scaramuzzino, Chiara Cuoc, Emeline C. Pla, Patrick Humbert, Sandrine Saudou, Frédéric |
author_facet | Scaramuzzino, Chiara Cuoc, Emeline C. Pla, Patrick Humbert, Sandrine Saudou, Frédéric |
author_sort | Scaramuzzino, Chiara |
collection | PubMed |
description | When a neurotrophin binds at the presynapse, it sends survival signals all the way to the nucleus on signaling endosomes. These endosomes fuel their own journey with on-board glycolysis—but how is that journey initiated and maintained? Using microfluidic devices and mice, we find that the calcium released upon brain-derived neurotrophic factor (BDNF) binding to its receptor, tropomyosin receptor kinase B (TrkB), is sensed by calcineurin on the cytosolic face of the endosome. Calcineurin dephosphorylates huntingtin, the BDNF scaffold, which sets the endosome moving in a retrograde direction. In an in vitro reconstituted microtubule transport system, controlled calcium uncaging prompts purified vesicles to move to the microtubule minus end. We observed similar retrograde waves of TrkA- and epidermal growth factor receptor (EGFR)-bearing endosomes. Signaling endosomes in neurons thus carry not only their own fuel, but their own navigational system. |
format | Online Article Text |
id | pubmed-8730605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-87306052022-01-19 Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus Scaramuzzino, Chiara Cuoc, Emeline C. Pla, Patrick Humbert, Sandrine Saudou, Frédéric Sci Adv Neuroscience When a neurotrophin binds at the presynapse, it sends survival signals all the way to the nucleus on signaling endosomes. These endosomes fuel their own journey with on-board glycolysis—but how is that journey initiated and maintained? Using microfluidic devices and mice, we find that the calcium released upon brain-derived neurotrophic factor (BDNF) binding to its receptor, tropomyosin receptor kinase B (TrkB), is sensed by calcineurin on the cytosolic face of the endosome. Calcineurin dephosphorylates huntingtin, the BDNF scaffold, which sets the endosome moving in a retrograde direction. In an in vitro reconstituted microtubule transport system, controlled calcium uncaging prompts purified vesicles to move to the microtubule minus end. We observed similar retrograde waves of TrkA- and epidermal growth factor receptor (EGFR)-bearing endosomes. Signaling endosomes in neurons thus carry not only their own fuel, but their own navigational system. American Association for the Advancement of Science 2022-01-05 /pmc/articles/PMC8730605/ /pubmed/34985962 http://dx.doi.org/10.1126/sciadv.abj8812 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Neuroscience Scaramuzzino, Chiara Cuoc, Emeline C. Pla, Patrick Humbert, Sandrine Saudou, Frédéric Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus |
title | Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus |
title_full | Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus |
title_fullStr | Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus |
title_full_unstemmed | Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus |
title_short | Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus |
title_sort | calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730605/ https://www.ncbi.nlm.nih.gov/pubmed/34985962 http://dx.doi.org/10.1126/sciadv.abj8812 |
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