Microglia cannibalism and efferocytosis leads to shorter lifespans of developmental microglia
- bioRxiv. 2024 Aug 29:2023.03.15.532426. doi: 10.1101/2023.03.15.532426.
- 1. Department of Biological Sciences, at the University of Notre Dame, Notre Dame, IN.
- 2. The Center for Stem Cells and Regenerative Medicine at the University of Notre Dame, Notre Dame, IN.
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, necroptosis-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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Research Areas: Cancer