引用本文:蓝瑞隆,张 娜,陈瑞庆.MCT1和LDHB在荷乳腺癌小鼠髓系抑制性细胞中的表达及意义[J].大连医科大学学报,2017,39(6):532-535.
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MCT1和LDHB在荷乳腺癌小鼠髓系抑制性细胞中的表达及意义
蓝瑞隆1,2, 张 娜3, 陈瑞庆1,2
1.福建医科大学附属第一医院 中心实验室,福建 福州 350005;2.福建省个体化主动免疫治疗重点实验室,福建 福州 350005;3.福建省血液病研究所 福建省血液病学重点实验室 福建医科大学附属协和医院,福建 福州 350001
摘要:
目的比较正常小鼠和荷乳腺癌小鼠骨髓中髓系抑制性细胞(MDSCs)的含量,探讨其产生免疫抑制功能的可能机制。方法建立荷乳腺癌小鼠模型,利用BD FACSAria Ⅲ流式分选仪分选正常小鼠组和荷乳腺癌小鼠组骨髓中的MDSCs(CD11b+ Gr-1+),比较其含量;q-PCR法检测两组MDSCs中MCT1及LDHB的mRNA水平。结果荷乳腺癌小鼠骨髓中MDSCs的比例为(48.92±3.13)%高于正常小鼠(25.13±1.95)%,差异有统计学意义(P<0.001);荷乳腺癌小鼠MDSCs中MCT1的mRNA相对表达量(0.010±0.005)为正常小鼠(0.003±0.001)的3.33倍,差异有统计学意义(P<0.05);荷乳腺癌小鼠MDSCs中LDHB的mRNA相对表达量(0.008±0.002)为正常小鼠(0.004±0.001)的2.00倍,差异极显著(P<0.01)。结论MDSCs在荷乳腺癌小鼠骨髓中的比例显著高于正常小鼠,其能量代谢关键分子MCT1、LDHB的表达也显著高于正常小鼠。MDSCs的能量代谢特点可能正是其发挥免疫抑制功能的重要基础。
关键词:  MDSC  MCT1  LDHB  能量代谢  免疫抑制
DOI:10.11724/jdmu.2017.06.03
分类号:R73
基金项目:基金项目:福建省卫计委青年课题(2016-1-60);2016年福建医科大学启航基金(2016QH042)
Expression and significance of MCT1 and LDHB in MDSCs  from bone marrow of breast cancer bearing mice
LAN Ruilong1,2, ZHANG Na3, CHEN Ruiqing1,2
1.Central Laboratory of the First Affiliated Hospital of Fujian Medical University,Fuzhou 350005,China;2.Fujian Key Laboratory of Individualized Active Immunotherapy,Fuzhou 350005,China;3.Fujian Insitute of Hematology, Fujian Provincial Key Laboratory on Hematology, Fujian Medical University Union Hospital,Fuzhou 350001,China
Abstract:
Objective To test the MDSCs ratios in bone marrow from normal and breast cancer bearing mice, and compare the mRNA levels of the key energy metabolism molecules-MCT1/LDHB and explore the possible mechanism of immunosuppression in MDSCs. Methods MDSCs (CD11b+ Gr-1+) in bone marrow was sorted by BD FACSAriaⅢ. MCT1/LDHB mRNA levels were detected with q-PCR. Results The MDSCs ratio (19.77±4.77)% in breast cancer bearing mice was much higher than that (0.84±0.18)% in normal group (P<0.001).Both MCT1 and LDHB mRNA of MDSCs in tumor bearing group were significantly higher than that in normal group (P<0.05 and P<0.01, respectively). Conclusions The energy metabolism could play an role in the immunosuppression of MDSCs.
Key words:  MDSC  MCT1  LDHB  energy metabolism  immunosuppression