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作 者:马倩茹[1] 张烽[1] 周桓[1] 於葛华[1] 张学光 顾宗江[2]
机构地区:[1]苏州大学医学院免疫学教研室,215007 [2]江苏省临床免疫学重点实验室
出 处:《中华微生物学和免疫学杂志》2006年第10期867-870,共4页Chinese Journal of Microbiology and Immunology
摘 要:目的探讨4-1BB(CD137)激发型单克隆抗体2A对小鼠骨髓来源的树突状细胞(DC)表面TLR4表达的调节。方法用不同剂量2A、LPS以及2A与LPS联合,或用LPS预刺激后再加入2A,以流式细胞术检测这些处理因素作用下DC表面TLR4表达情况。结果LPS可下调DC TLR4的表达,下调作用可维持24h,而2A可使DC TLR4的表达上调,上调作用可维持12h,并可拮抗LPS对TLR4的下调作用。用LPS预处理DC后再加入2A,也可拮抗LPS的下调作用。结论4-1BB信号可以上调DC表面TLR4的表达。Objective To study regulatory effect of agonist 4-1BB (CD137) monoclonal antibody 2A on TLR4 expression in murine dendritic cells (DC). Methods Flow cytometry was used to investigate the TLR4 expression on DC in following conditions: different doses of 2A, LPS, 2A combined with LPS, or addition of 2A after prestimulation of DC by LPS. Results LPS could down-regulate TLR4 expression on DC, and the down-regulatory effect of LPS was maintained for 24 h. On the contrary, 2A could up-regulate TLR4 expression on DC, and this effect was maintained for 12 h. Moreover, 2A inhibited the down-regulatory effect of LPS on TLR4 expression. When DC were stimulated by 2A after LPS prestimulation , 2A still up-regulated TLR 4 expression on DC. Conclusion 4-1BB signal can up-regulate the expression of TLR4 on dendritic cells.
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