卵巢癌细胞与巨噬细胞共培养对B7-H1表达的影响及机制  

The Effects of Ovarian Cancer Cells Co-cultured with Macrophages on the Expression of B7-H1 and Its Mechanisms

作　　者：熊海玉[1] 马婷婷[1] 王秦[1] 董晋豫[1] 梁勤东[1] 李紫微[1] 张维理[1] 涂植光[1] 

机构地区：[1]重庆医科大学检验医学院,临床检验诊断学教育部重点实验室,重庆400016

出　　处：《中国细胞生物学学报》2013年第12期1760-1764,共5页Chinese Journal of Cell Biology

基　　金：国家自然科学基金面上项目(批准号:81172016)资助的课题~~

摘　　要：为了探讨卵巢癌细胞与巨噬细胞共培养后对B7-H1表达的影响及其可能机制,利用佛波酯(PMA)诱导THP-1或外周血单核细胞分化为巨噬细胞后,与人卵巢癌细胞株SKOV3体外非接触共培养24 h,qRT-PCR、Western blot以及流式细胞术分别检测SKOV3与巨噬细胞B7-H1的表达;进一步利用NF-κB、JAK2/STAT3、p38 MAPK信号通路的抑制剂作用于共培养体系,检测B7-H1表达的变化,以探讨其机制。结果显示,共培养24 h后,SKOV3及巨噬细胞B7-H1 mRNA和蛋白的表达较非共培养组均显著升高(P<0.05),而阻断NF-κB、JAK2/STAT3、p38 MAPK信号通路后,B7-H1的上调均明显被抑制(P<0.05)。SKOV3与巨噬细胞共培养后B7-H1的表达升高(P<0.05),其机制可能涉及到NF-κB、JAK2/STAT3、p38 MAPK信号通路的激活。To investigate the effects of ovarian cancer cells co-cultured with macrophages on the expression of B7-H1 and its possible mechanisms, phorbol 12-myristate 13-acetate （PMA） treated THP-1 cells or human monocytes were co-cultured with human ovarian cancer cell line SKOV3 for 24 h in vitro without direct contact, the expression of B7-H1 in SKOV3 cells and macrophages was detected by qRT-PCR, Western blot and flow cytometry, respectively; In addition, the expression of B7-H1 was also determined after treating the coculture system with inhibitors of NF-κB, JAK2/STAT3 or p38 MAPK signal pathways. These results suggested that the expression of BT-H1 was significantly elevated at both mRNA and protein levels in SKOV3 and macrophages after coculture for 24 h （P〈0.05）. However, the upregulation of B7-H1 expression was inhibited by blocking NF-κB, JAK2/STAT3 or p38 MAPK signal pathways （P〈0.05）. SKOV3 cells co-cultured with macrophages promoted the expression of B7-H1 （P〈0.05）, which was possible involved in the activation of NF-nB, JAK2/STAT3, p38 MAPK signal pathways.

关 键 词：卵巢癌 B7-H1 肿瘤相关巨噬细胞 

分 类 号：R737.31[医药卫生—肿瘤]