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本文引用的文献

1
Glia actively sculpt sensory neurons by controlled phagocytosis to tune animal behavior.胶质细胞通过控制吞噬作用积极塑造感觉神经元,以调节动物行为。
Elife. 2021 Mar 24;10:e63532. doi: 10.7554/eLife.63532.
2
Microglia Inhibition Delays Retinal Degeneration Due to MerTK Phagocytosis Receptor Deficiency.小胶质细胞抑制因 MerTK 吞噬受体缺陷导致的视网膜变性。
Front Immunol. 2020 Jul 16;11:1463. doi: 10.3389/fimmu.2020.01463. eCollection 2020.
3
Local externalization of phosphatidylserine mediates developmental synaptic pruning by microglia.磷脂酰丝氨酸的局部外化介导小胶质细胞的发育性突触修剪。
EMBO J. 2020 Aug 17;39(16):e105380. doi: 10.15252/embj.2020105380. Epub 2020 Jul 13.
4
Microglia phagocytose myelin sheaths to modify developmental myelination.小胶质细胞吞噬髓鞘以修饰发育中的髓鞘形成。
Nat Neurosci. 2020 Sep;23(9):1055-1066. doi: 10.1038/s41593-020-0654-2. Epub 2020 Jul 6.
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Microglial Remodeling of the Extracellular Matrix Promotes Synapse Plasticity.小胶质细胞重塑细胞外基质促进突触可塑性。
Cell. 2020 Jul 23;182(2):388-403.e15. doi: 10.1016/j.cell.2020.05.050. Epub 2020 Jul 1.
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A splicing isoform of GPR56 mediates microglial synaptic refinement via phosphatidylserine binding.GPR56 的剪接异构体通过结合磷脂酰丝氨酸来调节小胶质细胞的突触修剪。
EMBO J. 2020 Aug 17;39(16):e104136. doi: 10.15252/embj.2019104136. Epub 2020 May 25.
7
IL-33-PU.1 Transcriptome Reprogramming Drives Functional State Transition and Clearance Activity of Microglia in Alzheimer's Disease.白细胞介素-33-PU.1转录组重编程驱动阿尔茨海默病中小胶质细胞的功能状态转变和清除活性
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Perisynaptic Schwann cells phagocytose nerve terminal debris in a mouse model of Guillain-Barré syndrome.施万细胞吞噬神经末梢碎片在格林-巴利综合征的小鼠模型中。
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9
The cell biology of the retinal pigment epithelium.视网膜色素上皮细胞生物学
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被神经胶质细胞吞噬:种间发育、功能和损伤中的神经胶质细胞修剪。

Engulfed by Glia: Glial Pruning in Development, Function, and Injury across Species.

机构信息

Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109.

Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, Washington 98195.

出版信息

J Neurosci. 2021 Feb 3;41(5):823-833. doi: 10.1523/JNEUROSCI.1660-20.2020. Epub 2021 Jan 19.

DOI:10.1523/JNEUROSCI.1660-20.2020
PMID:33468571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7880271/
Abstract

Phagocytic activity of glial cells is essential for proper nervous system sculpting, maintenance of circuitry, and long-term brain health. Glial engulfment of apoptotic cells and superfluous connections ensures that neuronal connections are appropriately refined, while clearance of damaged projections and neurotoxic proteins in the mature brain protects against inflammatory insults. Comparative work across species and cell types in recent years highlights the striking conservation of pathways that govern glial engulfment. Many signaling cascades used during developmental pruning are re-employed in the mature brain to "fine tune" synaptic architecture and even clear neuronal debris following traumatic events. Moreover, the neuron-glia signaling events required to trigger and perform phagocytic responses are impressively conserved between invertebrates and vertebrates. This review offers a compare-and-contrast portrayal of recent findings that underscore the value of investigating glial engulfment mechanisms in a wide range of species and contexts.

摘要

胶质细胞的吞噬活性对于神经系统的正常发育、回路的维持和大脑的长期健康至关重要。胶质细胞吞噬凋亡细胞和多余的连接,确保神经元连接得到适当的细化,同时清除成熟大脑中受损的突起和神经毒性蛋白,以防止炎症损伤。近年来,对不同物种和细胞类型的比较研究强调了控制胶质细胞吞噬的途径惊人的保守性。许多在发育修剪过程中使用的信号级联反应在成熟的大脑中被重新利用,以“微调”突触结构,甚至在创伤性事件后清除神经元碎片。此外,触发和执行吞噬反应所需的神经元-胶质细胞信号事件在无脊椎动物和脊椎动物之间惊人地保守。这篇综述提供了一个比较和对比的描述,突出了在广泛的物种和背景下研究胶质细胞吞噬机制的价值。