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核外层 lamin B 的局部翻译促进了轴突的维持。

Local translation of extranuclear lamin B promotes axon maintenance.

机构信息

Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.

出版信息

Cell. 2012 Feb 17;148(4):752-64. doi: 10.1016/j.cell.2011.11.064.

Abstract

Local protein synthesis plays a key role in regulating stimulus-induced responses in dendrites and axons. Recent genome-wide studies have revealed that thousands of different transcripts reside in these distal neuronal compartments, but identifying those with functionally significant roles presents a challenge. We performed an unbiased screen to look for stimulus-induced, protein synthesis-dependent changes in the proteome of Xenopus retinal ganglion cell (RGC) axons. The intermediate filament protein lamin B2 (LB2), normally associated with the nuclear membrane, was identified as an unexpected major target. Axonal ribosome immunoprecipitation confirmed translation of lb2 mRNA in vivo. Inhibition of lb2 mRNA translation in axons in vivo does not affect guidance but causes axonal degeneration. Axonal LB2 associates with mitochondria, and LB2-deficient axons exhibit mitochondrial dysfunction and defects in axonal transport. Our results thus suggest that axonally synthesized lamin B plays a crucial role in axon maintenance by promoting mitochondrial function.

摘要

局部蛋白质合成在调节树突和轴突中的刺激诱导反应中起着关键作用。最近的全基因组研究表明,数千种不同的转录本存在于这些远端神经元隔室中,但确定具有功能重要性的转录本是一项挑战。我们进行了一项无偏筛选,以寻找爪蟾视网膜神经节细胞 (RGC) 轴突中刺激诱导的、依赖蛋白质合成的蛋白质组变化。中间丝蛋白 lamin B2 (LB2) 通常与核膜相关,被鉴定为一个意想不到的主要靶标。轴突核糖体免疫沉淀证实了 lb2 mRNA 在体内的翻译。体内抑制 axon 中的 lb2 mRNA 翻译不会影响导向,但会导致轴突退化。轴突 LB2 与线粒体结合,LB2 缺陷的轴突表现出线粒体功能障碍和轴突运输缺陷。因此,我们的研究结果表明,在体内合成的 lamin B 作为一种关键蛋白,通过促进线粒体功能,在维持轴突方面发挥着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fa2/3314965/d17e30c689c5/fx1.jpg

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