首页|iMDCs干预重症肌无力小鼠模型的初步研究

iMDCs干预重症肌无力小鼠模型的初步研究

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目的:观察输注未成熟树突状细胞(iMDCs)干预重症肌无力小鼠模型(EAMG)的发病及Syk蛋白水平变化。方法:建立小鼠重症肌无力发病模型,采用iMDCs干预实验。健康雄性小鼠50只,随机分为模型组(A)20只、干预组(B)20只和对照组(C)10只。实验从初次免疫起至第90天终止,实验结束后行EAMG临床评估并进行脾脏和淋巴结Syk蛋白表达水平比较。结果:临床评估:A组发病率高于B组;实验终止时两组临床评分分别为1.69±1.12;0.35±0.67(P<0.01);C组小鼠无发病。A组小鼠的脾脏和淋巴结Syk蛋白表达水平较C组小鼠升高(P<0.01),B组较A组相比有所下降(P<0.05),但高于C组(P<0.05)。结论:输注iMDCs能够减轻重症肌无力小鼠临床症状及Syk蛋白表达,提示iMDCs干预能够调节EAMG免疫紊乱。
Objective:To observe the changes of pathogenesis and Syk protein levels on mice of myasthenia gravis model through intravenous injection of iMDCs. Methods:Establish a mouse model of experimental autoimmune myasthenia graves(EAMG), using iMDCs’ intervention. Using 50 healthy male mice, they were randomly divided into model group A of 20 , the intervention group B of 20 and control group C of 10. From the primary immune to 90th day of termination of the experiment, clinical evaluation were undergone, and every group’s Syk protein levels of spleen and lymph nodes were examined and compared. Results: The incidence of clinical assessment:group A was higher than that in group B. At the end of the experiment the clinical score in two groups were 1.69 ± 1.12 and 0.35 ± 0.67 (P<0.01). Group C showed no disease. Syk protein expression levels of spleen and lymph nodes of A elevated compared with C mice (P<0.01), group B decreased compared with group A (P<0.05), but higher than that of group C (P<0.05). Conclusion:Intravenous injection of iMDCs can reduce the clinical symptoms of myasthenia gravis in mice and Syk protein expression, suggesting iMDCs can regulate immune disorders of EAMG.

experimental autoimmune myasthenia graves(EAMG)immature bone marrow dendritic cells(iMDCs)Syk protein

王迎新、卢苗、董翔、陶定波、申敬顺

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大连医科大学附属第一医院神经内科 辽宁 大连 116011

实验性自身免疫性重症肌无力模型 未成熟树突状细胞 Syk蛋白

2013

中国保健营养(中旬刊)
全国卫生产业企业管理协会

中国保健营养(中旬刊)

ISSN:1004-7484
年,卷(期):2013.(9)
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