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小胶质细胞噬菌作用和吞噬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.

机构信息

Department of Biological Sciences at the University of Notre Dame, Notre Dame, Indiana, United States of America.

The Center for Stem Cells and Regenerative Medicine at the University of Notre Dame, Notre Dame, Indiana, United States of America.

出版信息

PLoS Biol. 2024 Oct 30;22(10):e3002819. doi: 10.1371/journal.pbio.3002819. eCollection 2024 Oct.

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

细胞的过度产生和随后的碎片产生是神经发育的普遍原则。在这里,我们展示了发育中神经系统的另一个特征,即胚胎小胶质细胞的牺牲性质导致神经碎片产生,这些小胶质细胞在清除其他神经碎片后不可逆地成为吞噬细胞。小胶质细胞被描述为寿命长,它们在胚胎大脑中定植并持续到成年。利用转基因斑马鱼研究大脑发育过程中的小胶质细胞碎片,我们发现与其他在扩张后在发育阶段死亡的神经细胞类型不同,在斑马鱼大脑中小胶质细胞扩张时,依赖于坏死性凋亡的小胶质细胞碎片是普遍存在的。对小胶质细胞的延时成像表明,这些碎片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作用的特征,我们使用延时成像和命运映射策略来跟踪个体发育中小胶质细胞的寿命。这些方法表明,胚胎小胶质细胞并不是长寿细胞,它们能完全消化其吞噬的碎片,相反,一旦斑马鱼中小胶质细胞中的大多数成为吞噬细胞,它们最终就会死亡,包括那些具有吞噬作用的细胞。这些结果建立了一个悖论——我们通过增加神经碎片和操纵吞噬作用来验证这个悖论——一旦胚胎中的大多数小胶质细胞成为吞噬细胞,它们就会死亡,产生碎片,然后被其他小胶质细胞吞噬,从而产生更多注定要死亡的吞噬性小胶质细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f73/11524473/b99b80f12dd7/pbio.3002819.g001.jpg

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