首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Role of IL-15 in spinal cord and sciatic nerve after chronic constriction injury: regulation of macrophage and T-cell infiltration.
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Role of IL-15 in spinal cord and sciatic nerve after chronic constriction injury: regulation of macrophage and T-cell infiltration.

机译:IL-15在慢性收缩损伤后在脊髓和坐骨神经中的作用:调节巨噬细胞和T细胞浸润。

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摘要

The release of inflammatory mediators from immune and glial cells either in the peripheral or CNS may have an important role in the development of physiopathological processes such as neuropathic pain. Microglial, then astrocytic activation in the spinal cord, lead to chronic inflammation, alteration of neuronal physiology and neuropathic pain. Standard experimental models of neuropathic pain include an important peripheral inflammatory component, which involves prominent immune cell activation and infiltration. Among potential immunomodulators, the T-cell cytokine interleukin-15 (IL-15) has a key role in regulating immune cell activation and glial reactivity after CNS injury. Here we show, using the model of chronic constriction of the sciatic nerve (CCI), that IL-15 is essential for the development of the early inflammatory events in the spinal cord after a peripheral lesion that generates neuropathic pain. IL-15 expression in the spinal cord was identified in both astroglial and microglial cells andwas present during the initial gliotic and inflammatory (NFkappaB) response to injury. The expression of IL-15 was also identified as a cue for macrophage and T-cell activation and infiltration in the sciatic nerve, as shown by intraneural injection of the cytokine and activity blockage approaches. We conclude that the regulation of IL-15 and hence the initial events following its expression after peripheral nerve injury could have a future therapeutic potential in the reduction of neuroinflammation.
机译:从周围或中枢神经系统的免疫和神经胶质细胞释放炎性介质可能在诸如神经性疼痛的生理病理过程的发展中起重要作用。小胶质细胞,然后脊髓中的星形细胞活化,导致慢性炎症,神经元生理学改变和神经性疼痛。神经性疼痛的标准实验模型包括重要的外周炎症成分,其涉及显着的免疫细胞活化和浸润。在潜在的免疫调节剂中,T细胞细胞因子白介素15(IL-15)在调节中枢神经系统损伤后的免疫细胞活化和神经胶质反应性中起关键作用。在这里,我们使用坐骨神经慢性收缩模型(CCI)显示,IL-15对于周围神经损伤后产生神经性疼痛的脊髓早期炎症事件的发展至关重要。在星形胶质细胞和小胶质细胞中都鉴定出了脊髓中的IL-15表达,并且在对损伤的初始神经胶质和炎性反应(NFkappaB)中存在。 IL-15的表达也被认为是巨噬细胞和T细胞在坐骨神经中活化和浸润的提示,如神经内注射细胞因子和活性阻滞方法所表明的。我们得出的结论是,IL-15的调节及其周围神经损伤后表达后的初始事件在减轻神经炎症方面可能具有未来的治疗潜力。

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