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作 者:李大主[1] 周游[1] 吴伟[1] 曾秋棠[1] 李裕舒[1] 王祥[1] 冯义柏[1] 曹林生[1]
机构地区:[1]华中科技大学同济医学院协和医院心内科,湖北武汉430022
出 处:《中国病理生理杂志》2006年第6期1079-1082,共4页Chinese Journal of Pathophysiology
基 金:湖北省卫生厅科研项目(No.NX200511)
摘 要:目的:探讨负载热休克蛋白60(HSP60)的致耐受性树突状细胞(DC)接种对ApoE-/-小鼠动脉粥样硬化斑块的影响。方法:制备ApoE-/-小鼠骨髓DC,分别用HSP60或HSP60加雷帕霉素(rap)处理获得DCHSP60和rap-DCHSP60,体外检测各组DC功能。分别用CFSE染色的DCHSP60和rap-DCHSP60及PBS经静脉接种高脂饲养ApoE-/-小鼠3次,末次接种后8周观察各组斑块面积,CD4+T细胞和DC在斑块中浸润情况及脾细胞对HSP60的反应。结果:体外HSP60负载DC CD86表达显著高于未负载DC,而致耐受DC CD86表达显著低于未负载DC。接种小鼠后,DCHSP60组斑块中炎性细胞浸润明显多于PBS组,DCHSP60组斑块面积大于PBS组;而rap-DCHSP60组炎性细胞浸润明显减少,斑块面积显著小于PBS组;HSP60刺激脾细胞后,DCHSP60组IFN-γ分泌增加,而rap-DCHSP6组IL-10分泌增加,反应呈抗原特异性。结论:负载HSP60的耐受性DC接种可抑制HSP60特异性免疫反应,抑制动脉粥样斑块中的炎症反应和斑块的进展。AIM: To evaluate whether tolerogenic dendritic cells (DC) loaded with heat shock protein 60 (HSP60) inhibit the progression of aortic atherosclerofic plaque in hypercholesterolemic apolipoprotein E (Apo- E) - null mice. METHODS: Bone marrow derived DC of the mice were loaded with HSP60 and co- cultured with rapamycin to generate tolerogenlc DC. The tolerogenic DC, DC loaded only HSP60 and PBS were injected into the ApoE - null mice at 8 weeks of age for three times at a one - week interval, 8 weeks after the last injection, aorta were harvested for HE staining and anti - CD4 + T cell immunostaining. Responses of plcenic cells to HSP60 were also evaluated. RESULTS: Compared with DC, DCHSP60 expressed higher levels of CD86, and stimulated T lymphocytes to proliferation significantly, while the tolerogenic DC expressed lower levels of CD86, and inhibited T lymphocytes to proliferation. After immunization with different injection, the numbers of CD4^+ T cells in plaque were increased significantly in DCHSP60 group vs in PBS group ( P 〈 0.01 ). On the other hand, they were reduced significantly in rap- DCHSP60 group vs in PBS group ( P 〈 0.01). Plaque axeas in the tolerogenic DC group were smaller than that in the PBS group ( P 〈 0.01). Stimulated by HSP60, plcenic cells in tolerogenic DC group secreted more IL- 10, while in DCHSP60 group more IFN- T secretion was observed. CONCLUSION: HSP60 specific tolerogenic DC immunization attenuated the progression of plaque, indicating a new immune therapy for atherosclerosis.
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