Department of Neurology, Multiple Sclerosis Research Center, Nashville, TN 37212, USA.
J Neuroimmunol. 2010 Dec 15;229(1-2):146-56. doi: 10.1016/j.jneuroim.2010.07.023. Epub 2010 Aug 19.
There are currently four known isoforms of nitric oxide synthase (NOS). Of these, neuronal NOS (nNOS) is known to be present exclusively in neurons, endothelial NOS (eNOS) in vascular endothelium, while the inducible form of NOS (iNOS) is known to be activated in oligodendrocytes, astrocytes and microglia. The fourth isoform, mitochondrial NOS (mtNOS), represents a post-translational modification of nNOS. Using western blotting and real time-PCR, we show induction and activation of nNOS following culture of oligodendrocyte progenitor cells (OPC) with lipopolysaccharide (LPS). Activation of nNOS results in accumulation of peroxynitrite and tyrosine nitration of proteins in oligodendrocytes resulting in reduced cell viability. Injection of LPS in vivo into the corpus callosum of rats leads to the development of extensive demyelination of the white matter tracts. Immunostaining of regions close to the injection site shows the presence of nNOS, but not iNOS, in oligodendrocytes. Neither iNOS nor nNOS was seen in astrocytes in areas of demyelination. These studies suggest that activation of nNOS in oligodendrocytes leads to oligodendrocyte injury resulting in demyelination.
目前已知有四种一氧化氮合酶(NOS)同工型。其中,神经元型 NOS(nNOS)仅存在于神经元中,内皮型 NOS(eNOS)存在于血管内皮中,而诱导型 NOS(iNOS)则存在于少突胶质细胞、星形胶质细胞和小胶质细胞中。第四种同工型,线粒体型 NOS(mtNOS),是 nNOS 的翻译后修饰形式。通过 Western blot 和实时 PCR,我们发现在脂多糖(LPS)培养少突胶质前体细胞(OPC)后,nNOS 被诱导和激活。nNOS 的激活导致过氧亚硝酸盐的积累和蛋白质的酪氨酸硝化,从而导致少突胶质细胞活力降低。体内向大鼠胼胝体注射 LPS 会导致白质束广泛脱髓鞘。在靠近注射部位的区域进行免疫染色显示,在少突胶质细胞中存在 nNOS,但不存在 iNOS。在脱髓鞘区域的星形胶质细胞中也未观察到 iNOS 或 nNOS。这些研究表明,少突胶质细胞中 nNOS 的激活导致少突胶质细胞损伤,从而导致脱髓鞘。