Mashayekhi F, Salehi Z
Prof. Farhad Mashayekhi, Department of Cell and Molecular Biology, Faculty of Biological Sciences, Tonekabon Branch, Islamic Azad University, Tonekabon, IR Iran, phone: 0098-9113330017, fax: 0098-131-3233647, e-mail:
Folia Neuropathol. 2016;54(3):259-264. doi: 10.5114/fn.2016.62535.
In the central nervous system (CNS) the main proteins of myelin are proteolipid protein (PLP), myelin basic protein (MBP), myelin oligodendrocyte glycoprotein (MOG) and CNPase. Myelin oligodendrocyte glycoprotein is a minor component of the myelin sheath, but is an important autoantigen linked to the pathogenesis of multiple sclerosis (MS). CNPase is expressed exclusively by oligodendrocytes in the CNS, and the appearance of CNPase seems to be one of the earliest events of oligodendrocyte differentiation and myelination. In this study the effects of vitamin D on total protein concentration, CNPase and MOG expression in the cerebral cortex of the murine model of cuprizone-induced demyelination was investigated. The mice were treated by cuprizone for five weeks in order to induce demyelination. The mice were then divided into 3 groups. The first group was injected intraperitoneally (IP) with vitamin D diluted in olive oil in the amount of 5 µg/kg/daily body weight. The second group (SHAM) was injected IP with olive oil and the third group was left without any injection as the control group (n = 11 for each group). After five weeks the mice were killed and the cerebral cortex was collected and the expression of CNPase and MOG was studied by Western blot. Total protein concentration in the vitamin D injected, SHAM and control groups were 0.918 ± 0.003, 0917 ± 0.004 and 0.916 ± 0.004 g/l, respectively (p > 0.05). However, a significant increase in the MOG and CNPase expression was seen in vitamin D injected group as compared to SHAM and control groups. It is concluded that vitamin D plays a role in the process of remyelination by increasing MOG and CNPase expression in the cortex.
在中枢神经系统(CNS)中,髓磷脂的主要蛋白质是蛋白脂蛋白(PLP)、髓磷脂碱性蛋白(MBP)、髓磷脂少突胶质细胞糖蛋白(MOG)和2',3'-环核苷酸3'-磷酸二酯酶(CNPase)。髓磷脂少突胶质细胞糖蛋白是髓鞘的次要成分,但却是与多发性硬化症(MS)发病机制相关的重要自身抗原。CNPase仅由中枢神经系统中的少突胶质细胞表达,CNPase的出现似乎是少突胶质细胞分化和髓鞘形成的最早事件之一。在本研究中,研究了维生素D对铜离子螯合剂诱导的脱髓鞘小鼠模型大脑皮质中总蛋白浓度、CNPase和MOG表达的影响。用铜离子螯合剂处理小鼠五周以诱导脱髓鞘。然后将小鼠分为3组。第一组腹腔注射(IP)以橄榄油稀释的维生素D,剂量为5μg/(kg·体重·天)。第二组(假手术组)腹腔注射橄榄油,第三组作为对照组不进行任何注射(每组n = 11)。五周后处死小鼠,收集大脑皮质,通过蛋白质免疫印迹法研究CNPase和MOG的表达。维生素D注射组、假手术组和对照组的总蛋白浓度分别为0.918±0.003、0.917±0.004和0.916±0.004g/L(p>0.05)。然而,与假手术组和对照组相比,维生素D注射组中MOG和CNPase的表达显著增加。得出的结论是,维生素D通过增加皮质中MOG和CNPase的表达在髓鞘再生过程中发挥作用。