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TrkA信号的光学激活

Optical Activation of TrkA Signaling.

作者信息

Duan Liting, Hope Jen M, Guo Shunling, Ong Qunxiang, François Amaury, Kaplan Luke, Scherrer Grégory, Cui Bianxiao

机构信息

Department of Chemistry , Stanford University , Stanford , California 94305 , United States.

Department of Anesthesiology, Perioperative and Pain Medicine, Department of Molecular and Cellular Physiology, Department of Neurosurgery , Stanford Neurosciences Institute, Stanford University , Palo Alto , California 94304 , United States.

出版信息

ACS Synth Biol. 2018 Jul 20;7(7):1685-1693. doi: 10.1021/acssynbio.8b00126. Epub 2018 Jul 12.

Abstract

Nerve growth factor/tropomyosin receptor kinase A (NGF/TrkA) signaling plays a key role in neuronal development, function, survival, and growth. The pathway is implicated in neurodegenerative disorders including Alzheimer's disease, chronic pain, inflammation, and cancer. NGF binds the extracellular domain of TrkA, leading to the activation of the receptor's intracellular kinase domain. As TrkA signaling is highly dynamic, mechanistic studies would benefit from a tool with high spatial and temporal resolution. Here we present the design and evaluation of four strategies for light-inducible activation of TrkA in the absence of NGF. Our strategies involve the light-sensitive protein Arabidopsis cryptochrome 2 and its binding partner CIB1. We demonstrate successful recapitulation of native NGF/TrkA functions by optical induction of plasma membrane recruitment and homo-interaction of the intracellular domain of TrkA. This approach activates PI3K/AKT and Raf/ERK signaling pathways, promotes neurite growth in PC12 cells, and supports survival of dorsal root ganglion neurons in the absence of NGF. This ability to activate TrkA using light bestows high spatial and temporal resolution for investigating NGF/TrkA signaling.

摘要

神经生长因子/原肌球蛋白受体激酶A(NGF/TrkA)信号传导在神经元发育、功能、存活和生长中起关键作用。该信号通路与包括阿尔茨海默病、慢性疼痛、炎症和癌症在内的神经退行性疾病有关。NGF与TrkA的细胞外结构域结合,导致受体细胞内激酶结构域的激活。由于TrkA信号传导具有高度动态性,因此机制研究将受益于具有高时空分辨率的工具。在此,我们展示了在无NGF情况下对TrkA进行光诱导激活的四种策略的设计和评估。我们的策略涉及光敏感蛋白拟南芥隐花色素2及其结合伴侣CIB1。我们通过光诱导TrkA细胞内结构域的质膜募集和同源相互作用,成功再现了天然NGF/TrkA的功能。这种方法激活了PI3K/AKT和Raf/ERK信号通路,促进了PC12细胞中的神经突生长,并在无NGF的情况下支持背根神经节神经元的存活。利用光激活TrkA的这种能力为研究NGF/TrkA信号传导赋予了高时空分辨率。

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