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机构地区:[1]中国科学技术大学生命科学学院免疫学研究所,合肥230027
出 处:《中国免疫学杂志》2005年第8期563-566,共4页Chinese Journal of Immunology
基 金:"973"项目(2001CB510000);国家自然基金项目(30230340);国家杰出青年科学基金-海外青年学者合作研究基金(30328022)资助
摘 要:目的:探讨低剂量刀豆蛋白A(ConA)预刺激对后续足剂量ConA诱导的小鼠肝炎的抑制作用。方法:足剂量ConA(15μg/g体重)静脉注射小鼠以诱导ConA肝炎模型。低剂量ConA预刺激组,在诱导ConA肝炎模型前12小时静脉注射低剂量ConA(3μg/g体重);PBS预处理对照组,在诱导ConA肝炎模型前12小时静脉注射PBS。观察两组血清转氨酶(ALT/AST)及肝脏病理变化,同时用流式细胞仪检测肝脏淋巴细胞亚群的比例及绝对数目变化。结果:与PBS预处理相比,低剂量ConA预刺激导致血清转氨酶(ALT/AST)水平显著降低(ALT由3433±788U/L降低到334±68U/L,AST由1358±297U/L降低到167±33U/L),肝脏病理切片显示由ConA引起的肝脏损伤明显减轻,同时伴随着肝脏内CD3+T淋巴细胞比例及绝对数目减少,并且其活化受到明显抑制。结论:低剂量ConA预刺激可以使小鼠抵抗后续的足剂量ConA诱导的肝脏损伤。这种现象与肝脏回流的T淋巴细胞减少及活化程度有关,其细胞与分子机制正在进一步探讨之中。Objective:To investigate the influence of concanavalin A(Con A) pretreagtment on the development of the fulminant murine hepatitis induced by an adequate dose of Con A. Methods: An adequate dose of Con A( 15μg/g. body. wt) was injected intravenously into C57BL/6 mice to provoke severe liver damage,an extensively-used murine hepatitis medel. A low dose of Con A(3μg/g.bedy.wt) was administrated intravenously 12 h before injection with an adequate dose of Con A. Liver injury was evaluated by serum transaminase assay and H&E staining. Hepatic lymphoeytes were analyzed by flow cytometry and the absolute amount of lymphocytes per liver was calculated. Results: Pretreatment with a low dose of Con A significantly inhibited Con A-induced liver injury. Both the percentage and the absolute number of liver CD3^+ T cells in Con A-pretreated mice were lower than those of PBS-pretreated mice. The activation of liver CD3^+ T cells in Con A-pretreated mice was also prominently inhibited. Concluslon:Con A pretreatrnent exerted the negative effect on the development of Con A-induced hepatitis,which may be result from the decreased recruitment of T ceils into the liver. The underlying mechanisms are under investigation.
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