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A paradox promoted by microglia cannibalism shortens the lifespan of developmental microglia

The overproduction of cells and subsequent production of debris is a universal principle of neurodevelopment. Here we show an additional feature of the developing nervous system that causes neural debris – promoted by the sacrificial nature of embryonic microglia that irreversibly become phagocytic...

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Detalles Bibliográficos
Autores principales: Gordon, Hannah, Schafer, Zachary T., Smith, Cody J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055159/
https://www.ncbi.nlm.nih.gov/pubmed/36993267
http://dx.doi.org/10.1101/2023.03.15.532426
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author Gordon, Hannah
Schafer, Zachary T.
Smith, Cody J.
author_facet Gordon, Hannah
Schafer, Zachary T.
Smith, Cody J.
author_sort Gordon, Hannah
collection PubMed
description The overproduction of cells and subsequent production of debris is a universal principle of neurodevelopment. Here we show an additional feature of the developing nervous system that causes neural debris – promoted by the sacrificial nature of embryonic microglia that irreversibly become phagocytic after clearing other neural debris. Described as long-lived, microglia colonize the embryonic brain and persist into adulthood. Using transgenic zebrafish to investigate the microglia debris during brain construction, we identified that unlike other neural cell-types that die in developmental stages after they have expanded, necroptotic-dependent microglial debris is prevalent when microglia are expanding in the zebrafish brain. Time-lapse imaging of microglia demonstrates that this debris is cannibalized by other microglia. To investigate features that promote microglia death and cannibalism, we used time-lapse imaging and fate-mapping strategies to track the lifespan of individual developmental microglia. These approaches revealed that instead of embryonic microglia being long-lived cells that completely digest their phagocytic debris, once most developmental microglia in zebrafish become phagocytic they eventually die, including ones that are cannibalistic. These results establish a paradox -- which we tested by increasing neural debris and manipulating phagocytosis -- that once most microglia in the embryo become phagocytic, they die, create debris and then are cannibalized by other microglia, resulting in more phagocytic microglia that are destined to die.
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spelling pubmed-100551592023-03-30 A paradox promoted by microglia cannibalism shortens the lifespan of developmental microglia Gordon, Hannah Schafer, Zachary T. Smith, Cody J. bioRxiv Article The overproduction of cells and subsequent production of debris is a universal principle of neurodevelopment. Here we show an additional feature of the developing nervous system that causes neural debris – promoted by the sacrificial nature of embryonic microglia that irreversibly become phagocytic after clearing other neural debris. Described as long-lived, microglia colonize the embryonic brain and persist into adulthood. Using transgenic zebrafish to investigate the microglia debris during brain construction, we identified that unlike other neural cell-types that die in developmental stages after they have expanded, necroptotic-dependent microglial debris is prevalent when microglia are expanding in the zebrafish brain. Time-lapse imaging of microglia demonstrates that this debris is cannibalized by other microglia. To investigate features that promote microglia death and cannibalism, we used time-lapse imaging and fate-mapping strategies to track the lifespan of individual developmental microglia. These approaches revealed that instead of embryonic microglia being long-lived cells that completely digest their phagocytic debris, once most developmental microglia in zebrafish become phagocytic they eventually die, including ones that are cannibalistic. These results establish a paradox -- which we tested by increasing neural debris and manipulating phagocytosis -- that once most microglia in the embryo become phagocytic, they die, create debris and then are cannibalized by other microglia, resulting in more phagocytic microglia that are destined to die. Cold Spring Harbor Laboratory 2023-03-16 /pmc/articles/PMC10055159/ /pubmed/36993267 http://dx.doi.org/10.1101/2023.03.15.532426 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Gordon, Hannah
Schafer, Zachary T.
Smith, Cody J.
A paradox promoted by microglia cannibalism shortens the lifespan of developmental microglia
title A paradox promoted by microglia cannibalism shortens the lifespan of developmental microglia
title_full A paradox promoted by microglia cannibalism shortens the lifespan of developmental microglia
title_fullStr A paradox promoted by microglia cannibalism shortens the lifespan of developmental microglia
title_full_unstemmed A paradox promoted by microglia cannibalism shortens the lifespan of developmental microglia
title_short A paradox promoted by microglia cannibalism shortens the lifespan of developmental microglia
title_sort paradox promoted by microglia cannibalism shortens the lifespan of developmental microglia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055159/
https://www.ncbi.nlm.nih.gov/pubmed/36993267
http://dx.doi.org/10.1101/2023.03.15.532426
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