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轴突起始段的内吞作用维持神经元极性。

Endocytosis in the axon initial segment maintains neuronal polarity.

机构信息

Howard Hughes Medical Institute, Department of Biology, Stanford University, Stanford, CA, USA.

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Nature. 2022 Sep;609(7925):128-135. doi: 10.1038/s41586-022-05074-5. Epub 2022 Aug 17.

Abstract

Neurons are highly polarized cells that face the fundamental challenge of compartmentalizing a vast and diverse repertoire of proteins in order to function properly. The axon initial segment (AIS) is a specialized domain that separates a neuron's morphologically, biochemically and functionally distinct axon and dendrite compartments. How the AIS maintains polarity between these compartments is not fully understood. Here we find that in Caenorhabditis elegans, mouse, rat and human neurons, dendritically and axonally polarized transmembrane proteins are recognized by endocytic machinery in the AIS, robustly endocytosed and targeted to late endosomes for degradation. Forcing receptor interaction with the AIS master organizer, ankyrinG, antagonizes receptor endocytosis in the AIS, causes receptor accumulation in the AIS, and leads to polarity deficits with subsequent morphological and behavioural defects. Therefore, endocytic removal of polarized receptors that diffuse into the AIS serves as a membrane-clearance mechanism that is likely to work in conjunction with the known AIS diffusion-barrier mechanism to maintain neuronal polarity on the plasma membrane. Our results reveal a conserved endocytic clearance mechanism in the AIS to maintain neuronal polarity by reinforcing axonal and dendritic compartment membrane boundaries.

摘要

神经元是高度极化的细胞,它们面临着将大量不同的蛋白质进行分隔以正常运作的基本挑战。轴突起始段(AIS)是一个特殊的区域,将神经元在形态、生物化学和功能上明显不同的轴突和树突分隔开来。AIS 如何维持这些隔室之间的极性尚不完全清楚。在这里,我们发现在秀丽隐杆线虫、小鼠、大鼠和人类神经元中,树突和轴突极化的跨膜蛋白被 AIS 中的内吞机制识别,被强烈内吞并靶向晚期内体进行降解。迫使受体与 AIS 的主要组织者,ankyrinG 相互作用,会拮抗 AIS 中的受体内吞作用,导致受体在 AIS 中积累,并导致随后的形态和行为缺陷,出现极性缺陷。因此,进入 AIS 的极化受体的内吞去除作为一种膜清除机制,可能与已知的 AIS 扩散屏障机制一起,共同维持质膜上的神经元极性。我们的研究结果揭示了 AIS 中一种保守的内吞清除机制,通过增强轴突和树突隔室的膜边界来维持神经元极性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b6c/9433327/931074734926/41586_2022_5074_Fig1_HTML.jpg

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