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吞噬基因促进秀丽隐杆线虫神经元再生:两种不同但互补的观点。

Engulfment Genes Promote Neuronal Regeneration in Caenorhabditis Elegans: Two Divergent But Complementary Views.

机构信息

Department of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607, USA.

Dept. of Biological Science, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Aichi Prefecture, Nagoya, 464-8602, Japan.

出版信息

Bioessays. 2020 Aug;42(8):e1900185. doi: 10.1002/bies.201900185. Epub 2020 Jun 11.

Abstract

Axon regeneration is a conserved process across the animal kingdom. Recent studies using the soil worm Caenorhabditis elegans as a model system revealed that machineries regulating engulfment of dying cells also control axon regeneration and axon debris removal. In this review, the relationships between the engulfment machinery and the biological processes triggered by axon injury and subsequent axon regeneration drawn from divergent views are examined. In one study, it is found that engulfing cells directly promote axon regeneration. In this context, CED-1 (Drosophila Draper/mouse MEGF10), an engulfment protein expressed on the surface of engulfing cells, functions as a receptor for axon debris removal and as an adhesion molecule for axon regeneration. In other studies, it is shown that those engulfment genes, previously known to function within the engulfing cells for cell corpse removal, can have a cell-autonomous "non-engulfing cell" role in axon regeneration. Together, these findings suggest that engulfment genes are repurposed for neuronal regeneration by acting in both engulfing cells and regenerating neurons.

摘要

轴突再生是动物界中普遍存在的过程。最近使用土壤线虫秀丽隐杆线虫作为模型系统的研究表明,调节死亡细胞吞噬的机制也控制着轴突再生和轴突碎片的清除。在这篇综述中,从不同的角度探讨了吞噬机制与轴突损伤和随后的轴突再生所引发的生物学过程之间的关系。在一项研究中,发现吞噬细胞可以直接促进轴突再生。在这种情况下,CED-1(果蝇 Draper/小鼠 MEGF10),一种在吞噬细胞表面表达的吞噬蛋白,作为轴突碎片清除的受体和轴突再生的黏附分子发挥作用。在其他研究中,表明先前已知在吞噬细胞内参与细胞尸体清除的吞噬基因,在轴突再生中具有细胞自主的“非吞噬细胞”作用。总之,这些发现表明,吞噬基因通过在吞噬细胞和再生神经元中发挥作用,被重新用于神经元再生。

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