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作 者:刘紫玲[1,2] 游晓星[1] 彭志平[2] 张慧丽[2] 高顺利[3] 曾焱华[1] 余敏君[1] 朱翠明[1]
机构地区:[1]南华大学医学微生物学与免疫学教研室,湖南衡阳421001 [2]包头市中心医院检验科,内蒙古包头014000 [3]南华大学附属第一医院,湖南衡阳421001
出 处:《细胞与分子免疫学杂志》2013年第1期10-13,共4页Chinese Journal of Cellular and Molecular Immunology
基 金:国家自然科学基金(81072418)
摘 要:目的研究肺炎支原体(Mp)荚膜多糖(CPS)与树突状细胞(DC)特异性细胞间黏附分子-3-结合非整合素分子(DC-SIGN,CD209)的相互作用及其对未成熟DC(iDC)分泌IL-10和IL-12的影响。方法提取并纯化Mp的CPS和脂质相关膜蛋白(LAMPs),用间接免疫荧光检测CPS与DC-SIGN受体的作用;ELISA法检测CPS和LAMPs作用后iDC所分泌的IL-10,IL-12水平。结果间接免疫荧光可见Mp CPS可结合到DC表面,且DC-SIGN的特异性封闭抗体可阻断CPS与DC的结合;ELISA检测发现CPS与LAMPs共孵育可促进DC分泌IL-10(P<0.05),而IL-12的表达水平刺激前后无统计学的差异。结论 Mp的CPS可识别并结合DC的DC-SIGN受体,并促进未成熟DC分泌IL-10。Objective To explore the interaction of Mycop/asma pneumoniae ( M. pneumoniae) capsular polysaccharide (CPS) with dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (DC-SIGN) and its influence on the secretions of IL-10 and IL-12. Methods M. pneurnoniae CPS and lipid-associated membrane proteins (LAMPs) were extracted and purified, and the specific binding of CPS and DC-SIGN was detected using indirect immunofluorescence stai- ning. The expressions of IL-10 and IL-12 was tested by ELISA in immature DC after treated by CPS or/and LAMPs. Results Indirect immunofluorescence staining showed CPS could recognized and bind specifically to the DC, which could be blocked by the DC-SIGN-specific blocking antibody. ELISA revealed that the production of immunosuppressive cytokine IL-10 increased when immature DC were stimulated by CPS, and the effect was more obvious with the presence of LAMPs( P 〈 0. 05). But the production of IL-12 did not change significantly after stimulation of CPS or/and LAMPs. Conclusion The CPS of M. pneumoniae can recognize and bind to the DC-SIGN specifically and promote the immature DC to secret IL-10.
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