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配体诱导 GPR110 激活促进损伤后的轴突生长。

Ligand-Induced GPR110 Activation Facilitates Axon Growth after Injury.

机构信息

Laboratory of Molecular Signaling, NIAAA, National Institutes of Health, 5625 Fishers Lane Room 3S-02, Rockville, MD 20892, USA.

Division of Pre-Clinical Innovation, NCATS, National Institutes of Health, Rockville, MD 20852, USA.

出版信息

Int J Mol Sci. 2021 Mar 25;22(7):3386. doi: 10.3390/ijms22073386.

Abstract

Recovery from axonal injury is extremely difficult, especially for adult neurons. Here, we demonstrate that the activation of G-protein coupled receptor 110 (GPR110, ADGRF1) is a mechanism to stimulate axon growth after injury. -docosahexaenoylethanolamine (synaptamide), an endogenous ligand of GPR110 that promotes neurite outgrowth and synaptogenesis in developing neurons, and a synthetic GPR110 ligand stimulated neurite growth in axotomized cortical neurons and in retinal explant cultures. Intravitreal injection of GPR110 ligands following optic nerve crush injury promoted axon extension in adult wild-type, but not in knockout, mice. In vitro axotomy or in vivo optic nerve injury rapidly induced the neuronal expression of . Activating the developmental mechanism of neurite outgrowth by specifically targeting GPR110 that is upregulated upon injury may provide a novel strategy for stimulating axon growth after nerve injury in adults.

摘要

轴突损伤的恢复极其困难,尤其是对于成年神经元。在这里,我们证明 G 蛋白偶联受体 110(GPR110,ADGRF1)的激活是损伤后刺激轴突生长的一种机制。-docosahexaenoylethanolamine(synaptamide)是 GPR110 的内源性配体,可促进发育神经元中的神经突生长和突触形成,而合成的 GPR110 配体可刺激轴突切断的皮质神经元和视网膜外植体培养物中的神经突生长。视神经挤压损伤后玻璃体内注射 GPR110 配体可促进成年野生型小鼠,但不能促进 敲除小鼠的轴突延伸。体外轴突切断或体内视神经损伤可迅速诱导神经元表达 。通过特异性靶向 GPR110 激活神经突生长的发育机制,该机制在损伤后上调,可能为成年后神经损伤后的轴突生长提供一种新的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63eb/8037074/9a6d9f92ed0e/ijms-22-03386-g001.jpg

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