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脊髓运动神经元中 Trk 受体的转激活。

Transactivation of Trk receptors in spinal motor neurons.

机构信息

Department of Biological Sciences, Hunter College, City University of New York, New York, NY, USA.

出版信息

Histol Histopathol. 2010 Sep;25(9):1207-13. doi: 10.14670/HH-25.1207.

Abstract

The neurotrophins are a family of trophic factors that have been shown to have neuroprotective effects after traumatic lesions of the nervous system and in animal models of neurodegenerative diseases. They mediate a broad spectrum of biological actions by interacting with tyrosine kinase receptors (Trk). While studies have demonstrated that neurotrophin administration may have beneficial effects, there were difficulties in delivering therapeutic quantities of these factors to spinal motor neurons. We now describe a strategy for applying transactivation of Trk receptors using small molecules, such as adenosine, which can penetrate the blood brain barrier and rescue motor neurons from cell death. Transactivation opens up the possibility of stimulating Trk receptors only in populations of neurons that co-express both Trk and adenosine receptors. We propose in this review to exploit transactivation to improve the survival of motor neurons in a transgenic mouse model of ALS and for other neurodegenerative diseases, such as Alzheimer's and Huntington's disease.

摘要

神经营养因子是一类营养因子,已被证明在神经系统创伤性损伤后和神经退行性疾病的动物模型中具有神经保护作用。它们通过与酪氨酸激酶受体(Trk)相互作用来介导广泛的生物学作用。虽然研究表明神经营养因子的给药可能具有有益的效果,但将这些因子的治疗剂量递送到脊髓运动神经元存在困难。我们现在描述了一种使用小分子(如腺苷)激活 Trk 受体的策略,这些小分子可以穿透血脑屏障并使运动神经元免于死亡。转激活为仅在共同表达 Trk 和腺苷受体的神经元群体中刺激 Trk 受体开辟了可能性。在这篇综述中,我们提出利用转激活来改善 ALS 的转基因小鼠模型以及其他神经退行性疾病(如阿尔茨海默病和亨廷顿病)中运动神经元的存活。

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