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小胶质细胞的自噬和噬菌作用导致发育中小胶质细胞的寿命缩短。

Microglia cannibalism and efferocytosis leads to shorter lifespans of developmental microglia.

作者信息

Gordon Hannah, Schafer Zachary, Smith Cody J

机构信息

Department of Biological Sciences, at the University of Notre Dame, Notre Dame, IN.

The Center for Stem Cells and Regenerative Medicine at the University of Notre Dame, Notre Dame, IN.

出版信息

bioRxiv. 2024 Aug 29:2023.03.15.532426. doi: 10.1101/2023.03.15.532426.

Abstract

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.

摘要

细胞的过度生成以及随后碎片的产生是神经发育的普遍规律。在此,我们展示了发育中神经系统的另一个特征,即导致神经碎片产生的特征——这是由胚胎小胶质细胞的牺牲性本质所推动的,这些小胶质细胞在清除其他神经碎片后会不可逆地转变为具有吞噬作用。小胶质细胞被描述为长寿细胞,它们在胚胎大脑中定植并持续存在至成年期。利用转基因斑马鱼来研究大脑构建过程中的小胶质细胞碎片,我们发现,与其他在发育阶段扩张后死亡的神经细胞类型不同,当斑马鱼大脑中的小胶质细胞在扩张时,坏死性凋亡依赖的小胶质细胞碎片很普遍。小胶质细胞的延时成像显示,这种碎片会被其他小胶质细胞吞噬。为了研究促进小胶质细胞死亡和吞噬的特征,我们使用延时成像和命运图谱策略来追踪单个发育中小胶质细胞的寿命。这些方法揭示,斑马鱼中的大多数发育中小胶质细胞一旦具有吞噬作用最终就会死亡,包括那些具有吞噬同类细胞行为的小胶质细胞,而不是胚胎小胶质细胞是能够完全消化其吞噬碎片的长寿细胞。这些结果产生了一个悖论——我们通过增加神经碎片和操纵吞噬作用来进行验证——即胚胎中的大多数小胶质细胞一旦具有吞噬作用,它们就会死亡、产生碎片,然后被其他小胶质细胞吞噬,从而导致更多注定要死亡的具有吞噬作用的小胶质细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a105/11423254/5a80e2dbe59a/nihpp-2023.03.15.532426v2-f0001.jpg

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