4-1BB Protects Dendritic Cells from Prostate Cancer-Induced Apoptosis

被引:6
作者
Kuang Youlin [1 ]
Zhang Jianwei [2 ]
Gou Xin [3 ]
Zhang Li [4 ]
Weng Xiaodong [4 ]
Liu Xiuheng [4 ]
Zhu Hengchen [4 ]
Chen Zhiyuan [4 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Urol, Chongqing 400016, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Urol, Zhengzhou, Peoples R China
[3] Chongqing Med Univ, Affiliated Hosp 1, Dept Urol, Chongqing 400016, Peoples R China
[4] Wuhan Univ, Renmin Hosp, Dept Urol, Wuhan 430072, Peoples R China
关键词
Dendritic cells; Co-stimulatory molecules; 4-1BB; Prostate cancer; EXPRESSION; IMMUNOTHERAPY; SURVIVAL; TUMORS; CD137;
D O I
10.1007/s12253-012-9566-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It has been shown that human prostate cancer (PCa) cells induced apoptotic death of the most potent antigen-presenting cells, dendritic cells (DCs), which are responsible for the induction of specific antitumor immune responses. Here, we investigated the function of 4-1BB on protecting DCs from prostate cancer-induced apoptosis with an agonistic mAb to 4-1BB. RM-1 cells and DCs were co-incubated for 48 h and DC apoptosis was assessed by Annexin Vassay. TNF-alpha and IL-12 production were assessed by enzyme-linked immunosorbent assay (ELISA) and Bcl-2 and Bcl-xL on DCs were analyzed by Western blot. We have shown that co-incubation of RM-1 cells with DCs is accompanied by an increased level of DCs apoptosis. Triggering 4-1BB on DCs resulted in increased resistance of DCs to RM-1 cells-induced apoptosis, which was owing to the up-regulated expression of Bcl-2 and Bcl-xL, and increased secretion of TNF-alpha and IL-12. These results demonstrate that triggering 4-1BB on DCs could increased resistance of DCs to PCa-induced apoptosis.
引用
收藏
页码:177 / 181
页数:5
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