Baron P, Constantin G, Meda L, Scarpini E, Scarlato G, Trinchieri G, Monastra G, Rossi F, Cassatella M A
Institute of Neurology, Dino Ferrari Center, University of Milan, IRCCS Ospedale Maggiore Policlinico, Italy.
Neurosci Lett. 1998 Aug 21;252(3):151-4. doi: 10.1016/s0304-3940(98)00497-2.
In human cultured monocytes we examined the ability of myelin basic protein (MBP) to induce the production of proinflammatory cytokines potentially involved in inflammatory demyelination. Northern blots and specific immunoassays demonstrated that monocytes incubated with optimal doses of MBP showed increased mRNA expression and release of tumor necrosis factor (TNF-alpha), interleukin-1beta (IL-1beta), interleukin-6 (IL-6), interleukin-8 (IL-8) but not of interleukin-12/p40 (IL-12/p40). We also showed that cytokine production by MBP-stimulated monocytes was abrogated by incubation with Dexamethasone. These data suggest that interaction of mononuclear phagocytes with MBP may participate in the regulatory process of cytokine production during inflammatory demyelination and support the beneficial role of corticosteroids therapy in aberrant immune responses to the myelin sheath.
在人类培养的单核细胞中,我们检测了髓鞘碱性蛋白(MBP)诱导可能参与炎性脱髓鞘的促炎细胞因子产生的能力。Northern印迹和特异性免疫分析表明,用最佳剂量的MBP孵育的单核细胞显示肿瘤坏死因子(TNF-α)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)的mRNA表达和释放增加,但白细胞介素-12/p40(IL-12/p40)未增加。我们还表明,用MBP刺激的单核细胞产生的细胞因子在与地塞米松孵育后被消除。这些数据表明,单核吞噬细胞与MBP的相互作用可能参与炎性脱髓鞘过程中细胞因子产生的调节过程,并支持皮质类固醇疗法在对髓鞘异常免疫反应中的有益作用。