5. T cell immunity and neuroplasticity.

Zhi Huang, Grace K Ha, John M Petitto
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Abstract

The proneuronal effects of T cells that impact the brain occur from both T cells trafficking into the brain, and from signals in the periphery (e.g., cytokine release and regulation). Recent data indicates that neuroimmunological changes in the brain can modify intrinsic brain processes that are involved in regulating neuroplasticity (e.g., T-cell/microglial interactions, neurotrophins, neurogenesis). We describe: 1) work from our lab and others showing that injury-induced loss of neuronal phenotype and reversal of motor neuron atrophy are associated with normal T cell immunity, and; 2) research indicating that these and other neuroimmunological processes may be generalizable to mechanisms of neuroplasticity involved in cognitive and emotional behavior. These findings are discussed in relation to our lab's working hypothesis, that T cell immunosenesence may contribute to alterations in brain neuroplasticity related to aging. Greater understanding of the role of adaptive T cell immunity on neuroplasticity could have important clinical implications for developing novel treatment strategies for neurodegenerative diseases (e.g., Alzheimer's) and brain injury (e.g., stroke, trauma).

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5. T细胞免疫和神经可塑性。
T细胞影响大脑的前神经元效应既来自于T细胞进入大脑,也来自于外周的信号(例如,细胞因子的释放和调节)。最近的数据表明,大脑中的神经免疫学变化可以改变参与调节神经可塑性的内在大脑过程(例如,t细胞/小胶质细胞相互作用,神经营养物质,神经发生)。我们描述:1)我们的实验室和其他人的研究表明,损伤引起的神经元表型丧失和运动神经元萎缩的逆转与正常的T细胞免疫有关;2)研究表明,这些和其他神经免疫过程可以推广到涉及认知和情绪行为的神经可塑性机制。这些发现与我们实验室的工作假设有关,即T细胞免疫衰老可能有助于与衰老相关的脑神经可塑性的改变。更好地了解适应性T细胞免疫对神经可塑性的作用,可能对开发神经退行性疾病(如阿尔茨海默氏症)和脑损伤(如中风、创伤)的新治疗策略具有重要的临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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5. T cell immunity and neuroplasticity.
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