Department of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH, 03824, USA.
Department of Chemistry, University of Alaska Anchorage, Anchorage, AK, 99508, USA.
Neuromolecular Med. 2021 Mar;23(1):25-46. doi: 10.1007/s12017-021-08646-2. Epub 2021 Feb 5.
Neuro-inflammation accompanies numerous neurological disorders and conditions where it can be associated with a progressive neurodegenerative pathology. In a similar manner, alterations in sphingolipid metabolism often accompany or are causative features in degenerative neurological conditions. These include dementias, motor disorders, autoimmune conditions, inherited metabolic disorders, viral infection, traumatic brain and spinal cord injury, psychiatric conditions, and more. Sphingolipids are major regulators of cellular fate and function in addition to being important structural components of membranes. Their metabolism and signaling pathways can also be regulated by inflammatory mediators. Therefore, as certain sphingolipids exert distinct and opposing cellular roles, alterations in their metabolism can have major consequences. Recently, regulation of bioactive sphingolipids by neuro-inflammatory mediators has been shown to activate a neuronal NADPH oxidase 2 (NOX2) that can provoke damaging oxidation. Therefore, the sphingolipid-regulated neuronal NOX2 serves as a mechanistic link between neuro-inflammation and neurodegeneration. Moreover, therapeutics directed at sphingolipid metabolism or the sphingolipid-regulated NOX2 have the potential to alleviate neurodegeneration arising out of neuro-inflammation.
神经炎症伴随着许多神经紊乱和疾病,它可能与进行性神经退行性病理有关。同样,鞘脂代谢的改变通常伴随着神经退行性疾病,或者是其致病特征。这些疾病包括痴呆、运动障碍、自身免疫性疾病、遗传性代谢紊乱、病毒感染、颅脑和脊髓损伤、精神疾病等。鞘脂不仅是膜的重要结构成分,还是细胞命运和功能的主要调节剂。它们的代谢和信号通路也可以被炎症介质调节。因此,由于某些鞘脂发挥着独特且相反的细胞作用,其代谢的改变可能会产生重大影响。最近,神经炎症介质对生物活性鞘脂的调节已被证明可以激活神经元 NADPH 氧化酶 2(NOX2),从而引发破坏性氧化。因此,鞘脂调节的神经元 NOX2 是神经炎症和神经退行性变之间的机制联系。此外,针对鞘脂代谢或鞘脂调节的 NOX2 的治疗方法有可能缓解神经炎症引起的神经退行性变。