Neuroscience Graduate Program, University of Michigan, Ann Arbor, MI, United States; Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA, United States.
Curr Opin Neurobiol. 2013 Oct;23(5):806-11. doi: 10.1016/j.conb.2013.02.003. Epub 2013 Feb 26.
The reciprocal interactions between sleep and immune function are well-studied. Insufficient sleep induces innate immune responses as evidenced by increased expression of pro-inflammatory mediators in the brain and periphery. Conversely, immune challenges upregulate immunomodulator expression, which alters central nervous system-mediated processes and behaviors, including sleep. Recent studies indicate that glial cells, namely microglia and astrocytes, are active contributors to sleep and immune system interactions. Evidence suggests glial regulation of these interactions is mediated, in part, by adenosine and adenosine 5'-triphosphate actions at purinergic type 1 and type 2 receptors. Furthermore, microglia and astrocytes may modulate declines in sleep-wake behavior and immunity observed in aging.
睡眠与免疫功能之间的相互作用已经得到了充分的研究。睡眠不足会引起先天免疫反应,这表现在大脑和外周组织中促炎介质的表达增加。相反,免疫挑战会上调免疫调节剂的表达,从而改变中枢神经系统介导的过程和行为,包括睡眠。最近的研究表明,神经胶质细胞,即小胶质细胞和星形胶质细胞,是睡眠和免疫系统相互作用的积极贡献者。有证据表明,这些相互作用的神经胶质调节部分是由嘌呤能 1 型和 2 型受体的腺苷和腺苷 5'-三磷酸作用介导的。此外,小胶质细胞和星形胶质细胞可能调节衰老过程中观察到的睡眠-觉醒行为和免疫功能下降。