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人初始和记忆CD4^+T细胞信使RNA基因芯片检测结果分析 被引量:3

Analysis of the messenger RNA from human naive and memory CD4^+ T cells by gene chips
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摘要 目的探讨健康成人外周血初始和记忆CD4^+T细胞静息状态下表面分子、趋化因子受体、细胞因子和转录因子mRNA表达的差异。方法抽取健康成年人外周血,分离PBMC,染色后流式分选出CD45RO-的初始和CD45RO+的记忆CD4^+T细胞,裂解细胞,进行mRNA表达谱芯片检测。结果相比初始T细胞,静息状态下记忆CD4^+T细胞表达高水平的表面分子CTLA-4、PD-1、FAS、CD25,趋化因子受体CCR4、CCR6、CXCR3、CXCR5,细胞因子IFN-γ、TNF-α、IL-17和转录因子T-bet、EOMES、STAT4、GATA3和RORγt,并表达低水平的表面分子CD62L、CCR7、ICAM-I、CD40L,细胞因子IL-1β和转录因子NF-κB。结论静息状态下,与初始CD4^+T细胞相比,记忆CD4^+T细胞高表达某些活化分子、细胞因子、转录因子mRNA,可能是记忆CD4^+T细胞发生快速免疫应答的关键因素。 This study was designed to investigate the difference in mRNA expression of surface molecules,chemokine receptors, cytokines and transcription factors between na?ve and memory CD4^+ T cells from peripheral blood of healthy adults. Peripheral blood of healthy adults were collected to isolate PBMCs, and then, CD45 ROnaive and CD45 RO+ memory CD4^+ T cells were sorted from PBMCs by flow cytometry. The sorted cells were lysed and the detection of mRNA expression was performed. Data showed that compared to naive CD4^+ T cells, memory CD4^+ T cells expressed higher levels of surface molecules(CTLA-4, PD-1, FAS, CD25), chemokine receptors(CCR4, CCR6, CXCR3, CXCR5), cytokines(IFN-γ, TNF-α, IL-17) and transcription factors T-bet, EOMES,STAT4, GATA3 as well as RORγt. In addition, memory CD4^+ T cells expressed lower levels of surface molecules(CD62 L, CCR7, ICAM-I, CD40 L), cytokine IL-1β and transcription factor NF-κB. Taken together, the higher expression of mRNA by memory CD4^+ T cells than naive CD4^+ T cells on the activation molecules, cytokines and transcriptional factors in resting status indicate the faster immune response of memory CD4^+ T cells than naive CD4^+ T cells.
作者 康双朋 余思菲 吴琼丽 金水平 樊莉 万顺巧 吴长有 KANG Shuangpeng;YU Sifei;WU Qiongli;JIN Shuiping;FAN Li;WAN Shunqiao;WU Changyou(Guangdong Provincial Key Laboratory of Organ Transplantation&Institute of Immunology,Zhongshan School of Medicine,Sun Yat-sen University,Guangzhou 510080,China)
出处 《免疫学杂志》 CAS CSCD 北大核心 2020年第5期422-425,共4页 Immunological Journal
基金 国家自然科学基金面上项目(31670900,81971556)。
关键词 记忆T细胞 CD4^+T细胞 MRNA Memory T cells CD4^+T cells mRNA
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  • 1吴长有.免疫记忆与疫苗研究开发[J].中国免疫学杂志,2005,21(1):4-7. 被引量:29
  • 2吴长有.初始和记忆T细胞的研究进展[J].现代免疫学,2005,25(5):353-356. 被引量:32
  • 3李丽,吴长有.Th1细胞的分化、多样性、记忆细胞的形成及对疫苗研究的意义[J].中国免疫学杂志,2006,22(7):680-681. 被引量:6
  • 4Biswas PS, Pedicord V, Ploss A, et al. Pathogen-specific CD8 T cell responses are directly inhibited by IL-10. J Immunol, 2007, 179(7): 4520-8.
  • 5Kondrack RM, Harbertson J, Tan JT, et al. Interleukin 7 regulates the survival and generation of memory CD4 cells. J Exp Med, 2003, 198(12): 1797-806.
  • 6Osbome LC, Dhanji S, Snow JW,et al. Impaired CD8 T cell memory and CD4 T cell primary responses in IL-7R α mutant mice. J Exp Med, 2007, 204(3): 619-31.
  • 7Sun JC, Lehar SM, Bevan MJ. Augmented IL-7 signaling during viral infection drives greater expansion of effector T cells but does not enhance memory. J Ilnmunol, 2006, 177 (7): 4458-63.
  • 8Yajima T, Yoshihara K, Nakazato K, et al. IL-15 regulates CD8+T cell contraction during primary infection. J Immunol, 2006, 176(1): 507-15.
  • 9Melchionda F, Fry TJ, Milliron MJ, et al. Adjuvant IL-7 or IL-15 overcomes immunodominance and improves survival of the CD8+ memory cell pool. J Clin Invest, 2005, 115(5): 1177-87.
  • 10Nanjappa SG, Walent JH, Morre M, et al. Effects of IL-7 on memory CD8 T cell homeostasis are influenced by the timing of therapy in mice. J Clin Invest, 2008, 118(3): 1027-39.

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