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Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction

Microglia are highly motile glial cells that are proposed to mediate synaptic pruning during neuronal circuit formation. Disruption of signaling between microglia and neurons leads to an excess of immature synaptic connections, thought to be the result of impaired phagocytosis of synapses by microgl...

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Autores principales: Weinhard, Laetitia, di Bartolomei, Giulia, Bolasco, Giulia, Machado, Pedro, Schieber, Nicole L., Neniskyte, Urte, Exiga, Melanie, Vadisiute, Auguste, Raggioli, Angelo, Schertel, Andreas, Schwab, Yannick, Gross, Cornelius T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964317/
https://www.ncbi.nlm.nih.gov/pubmed/29581545
http://dx.doi.org/10.1038/s41467-018-03566-5
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author Weinhard, Laetitia
di Bartolomei, Giulia
Bolasco, Giulia
Machado, Pedro
Schieber, Nicole L.
Neniskyte, Urte
Exiga, Melanie
Vadisiute, Auguste
Raggioli, Angelo
Schertel, Andreas
Schwab, Yannick
Gross, Cornelius T.
author_facet Weinhard, Laetitia
di Bartolomei, Giulia
Bolasco, Giulia
Machado, Pedro
Schieber, Nicole L.
Neniskyte, Urte
Exiga, Melanie
Vadisiute, Auguste
Raggioli, Angelo
Schertel, Andreas
Schwab, Yannick
Gross, Cornelius T.
author_sort Weinhard, Laetitia
collection PubMed
description Microglia are highly motile glial cells that are proposed to mediate synaptic pruning during neuronal circuit formation. Disruption of signaling between microglia and neurons leads to an excess of immature synaptic connections, thought to be the result of impaired phagocytosis of synapses by microglia. However, until now the direct phagocytosis of synapses by microglia has not been reported and fundamental questions remain about the precise synaptic structures and phagocytic mechanisms involved. Here we used light sheet fluorescence microscopy to follow microglia–synapse interactions in developing organotypic hippocampal cultures, complemented by a 3D ultrastructural characterization using correlative light and electron microscopy (CLEM). Our findings define a set of dynamic microglia–synapse interactions, including the selective partial phagocytosis, or trogocytosis (trogo-: nibble), of presynaptic structures and the induction of postsynaptic spine head filopodia by microglia. These findings allow us to propose a mechanism for the facilitatory role of microglia in synaptic circuit remodeling and maturation.
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spelling pubmed-59643172018-05-24 Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction Weinhard, Laetitia di Bartolomei, Giulia Bolasco, Giulia Machado, Pedro Schieber, Nicole L. Neniskyte, Urte Exiga, Melanie Vadisiute, Auguste Raggioli, Angelo Schertel, Andreas Schwab, Yannick Gross, Cornelius T. Nat Commun Article Microglia are highly motile glial cells that are proposed to mediate synaptic pruning during neuronal circuit formation. Disruption of signaling between microglia and neurons leads to an excess of immature synaptic connections, thought to be the result of impaired phagocytosis of synapses by microglia. However, until now the direct phagocytosis of synapses by microglia has not been reported and fundamental questions remain about the precise synaptic structures and phagocytic mechanisms involved. Here we used light sheet fluorescence microscopy to follow microglia–synapse interactions in developing organotypic hippocampal cultures, complemented by a 3D ultrastructural characterization using correlative light and electron microscopy (CLEM). Our findings define a set of dynamic microglia–synapse interactions, including the selective partial phagocytosis, or trogocytosis (trogo-: nibble), of presynaptic structures and the induction of postsynaptic spine head filopodia by microglia. These findings allow us to propose a mechanism for the facilitatory role of microglia in synaptic circuit remodeling and maturation. Nature Publishing Group UK 2018-03-26 /pmc/articles/PMC5964317/ /pubmed/29581545 http://dx.doi.org/10.1038/s41467-018-03566-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Weinhard, Laetitia
di Bartolomei, Giulia
Bolasco, Giulia
Machado, Pedro
Schieber, Nicole L.
Neniskyte, Urte
Exiga, Melanie
Vadisiute, Auguste
Raggioli, Angelo
Schertel, Andreas
Schwab, Yannick
Gross, Cornelius T.
Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
title Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
title_full Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
title_fullStr Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
title_full_unstemmed Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
title_short Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
title_sort microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964317/
https://www.ncbi.nlm.nih.gov/pubmed/29581545
http://dx.doi.org/10.1038/s41467-018-03566-5
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