期刊文献+

蛋白激酶Cθ在γδT细胞表达L-选择素中的调控作用

Effect of protein kinase CO on the regulation of L-selectin expression of human γδT cells
原文传递
导出
摘要 目的探讨蛋白激酶Cθ(PKCθ)信号转导途径在γδT细胞表达L-选择素(CD62L)中的调控作用。方法用结核分枝杆菌抗原(Mtb-Ag)刺激人外周血单个核细胞(PBMC)并培养6~8d,获得富含γδT细胞的结核分枝杆菌活化T细胞(MtbAT),作为γδT细胞来源,分别加佛波醇酯(PMA)、PMA+离子霉素(IMN)培养3、6、12、24h,或用培养8d的MtbAT细胞分别加入Mtb—Ag、Rottlerin+Mtb-Ag、PMA、Rottlerin+PMA刺激4h,收集细胞用荧光抗体染色后,流式细胞术(FCM)检测CD62L在18T细胞表面的表达。结果体外激活培养6~8d的18T细胞表面CD62L的表达率为75.0%~87.0%。PMA刺激78T细胞3~12h时CD62L表达逐渐下调,表达率为42.3%~25.5%;但在刺激后24h时,又明显回升至53.2%。而PMA+IMN刺激3、6h时,18T细胞CD62L表达也下调,表达率分别为52.1%、39.3%;但在刺激12h和24h时CD62L表达率分别为52.9%和35.3%。在PMA刺激γδT细胞同时加入Rottlerin,则CD62L的表达率(47.9%)明显高于PMA单独刺激组(31.8%);MtbAT用Mtb—Ag再刺激4h后,γδT细胞CD62L的表达率由70.0%降为54.8%,而在Mtb.Ag再刺激时加入Rottlerin,则CD62L表达率增加到63.1%。结论γδT细胞在PMA或Mtb-Ag刺激后CD62L的表达下调可被PKCθ特异性抑制剂部分阻断,表明CD62L在γδT细胞表面的表达可能与PKCθ信号转导途径的调控相关。 Objective To investigate the role of PKCθ signal pathway on regulation of L-selectin (CD62L) expression in human activated γδT cells. Methods Human peripheral blood mononuclear cells (PBMC) were stimulated with Mycobacterium tuberculosis antigen (Mtb-Ag) and cultured for 6-8 d to generate Mtb-Ag activated T cells(MtbAT) as γδT cells enrichment T cell line. The MtbAT were stimulated with PMA or PMA + IMN for 3, 6, 12 and 24 h, respectively, or MtbAT cultured for 8 d were stimulated with Mtb-Ag, or PMA, with or without PKC0 inhibitor Rotflerin for 4 h. After the treated cells stained with fluorescent labeled monoclonal antibodies, the expression of CD62L on "vST cells were measured by flow cytome- try (FCM). Results The expression of CD62L on γδT cells cultured for 6-8 d were 75.0% -87.0%. Decrease of CD62L from the surface of γδT cells by 3 h to 12 h after exposure to PMA (42.3% to 23.5% ), but CD62L expression increased to 53.2% when γδT cells were exposed to PMA for 24 h. The expression of CD62L of γδT cells decreased to 52.1% and 39.3% respectively when γδT cells were exposed to PMA + IMN for 3 h and 6 h. After treated with PMA + IMN for 12 h and 24 h, the expression of CD62L were 52.9% and 35. 3% respectively. The CD62L expression of γδT cells treated with PMA and Rottlerin (47.9%) were higher than that treated with PMA alone (31.8%). After Mtb-Ag restimulated MtbAT for 4 h, the CD62L level of γδT cells decreased from 70.0% to 54.8%, Rottlerin could inhibite Mtb-Ag down regulation CD62L level of γδT cells (63.1%). Conclusion The CD62L expression of γδT cells could be inhibited partly by the inhibitor of PKCθ, it suggested that PKC0 signal pathway may regulate L-selectin (CD62L) expression of activated human γδT cells.
出处 《中华微生物学和免疫学杂志》 CAS CSCD 北大核心 2009年第2期146-150,共5页 Chinese Journal of Microbiology and Immunology
基金 安徽省自然科学基金项目(050430603) 安徽省教育厅自然科学基金项目(KJ20078369ZC) 安徽省高等学校青年教师科研资助计划项目(2007jq1132) 蚌埠医学院科研基金项目(BY0508)
关键词 L-选择素 ΓΔT细胞 蛋白激酶C L-selectin γδT lymphocytes Protein kinase C
  • 相关文献

参考文献15

  • 1Picker LJ, Butcher EC. Physiological and molecular mechanisms of lymphocyte homing. Annu Rev Immunol, 1992, 10: 561-591. 被引量:1
  • 2Smith JA. Neutrophils, host defense, and inflammation: a double-edged sword. J Leukocyte Biol, 1994, 56(6) : 672-686. 被引量:1
  • 3Chao CC, Jensen R, Dailey MO. Mechanisms of L-selectin regulation by activated T cells. J Immunol, 1997, 159 (4) : 1686- 1694. 被引量:1
  • 4Richards H, Longhi MP, Wright K, et al. CD62L (L-selectin) down-regulation does not affect memory T cell distribution but failure to shed compromises anti-viral immunity. J Immunol, 2008, 180( 1 ) : 198-206. 被引量:1
  • 5Lee D, Schultz JB, Knauf PA, et al. Mechanical shedding of L- selectin from the neutrophil surface during rolling on sialyl Lewis x under flow. J Biol Chem, 2007, 282(7) : 4812-4820. 被引量:1
  • 6Gerli R, Gresele P, Bistoni O, et al. Salicylates inhibit T cell adhesion on endothelium under nonstatic conditions: induction of L-selectin shedding by a tyrosine kinase dependent mechanism. J Immunol, 2001, 166(3): 832-840. 被引量:1
  • 7Kaldjian EP, Stodman LM. Regulation of L-selectin mRNA in Jurkat cells. J Immunol, 1995, 154(4) : 4351-4362. 被引量:1
  • 8Karin K, Jens D, Eva CM, et al. The interaction of protein kinase C isozymes α,ι,θ with the cytoplasmic domain of L-selectin is modulated by phosphorylation of the receptor. J Biol Chem, 2004, 279(33): 34472-34480. 被引量:1
  • 9武文娟,沈继龙,李柏青.MtbAg体外激活扩增的人γδT细胞表面L-选择素的动态变化[J].蚌埠医学院学报,2005,30(3):192-194. 被引量:3
  • 10武文娟,李柏青.结核杆菌抗原诱导的人γδT细胞表达L-选择素的调控机制[J].现代免疫学,2006,26(5):413-417. 被引量:1

二级参考文献43

  • 1武文娟,沈继龙,李柏青.MtbAg体外激活扩增的人γδT细胞表面L-选择素的动态变化[J].蚌埠医学院学报,2005,30(3):192-194. 被引量:3
  • 2梅传忠,李柏青.PKC在结核杆菌抗原诱导人γδT细胞凋亡中的作用[J].现代免疫学,2005,25(6):441-444. 被引量:2
  • 3Chao CC, Jensen R, Dailey MO. Mechanisms of L-selectin regulation by activated T cells[J]. J Immunol, 1997,159 (4):1 686~1 694. 被引量:1
  • 4Picker LJ, Martin RJ, Trumble A, et al. Differential expression of lymphocyte homing receptors by human menory/effector T cells in pumonary versus cutaneous immue effector sites [ J ]. E J Immunol, 1994,24 (6): 1 269~1 277. 被引量:1
  • 5Boom WH,Balaji KN, Nayak R, et al. Characterization of a 10- to 14-kilodalton protease-sensitive Mycobacterium tuberculosis H37Ra antigen that stimulates human γδT cells [ J ]. Infect Immun ,1994,62 (12):5 511~5 518. 被引量:1
  • 6van Wely CA, Beverley PC, Brett SJ, et al. Expression of Lselectin on Th1 cells is regulated by IL-12[J]. J Immunol, 1999,163 (3):1 214~1 221. 被引量:1
  • 7Laurent M,Pado TB. T lymphocyte activation intiates the degradation of the CD62L encoding mRNA and increase the transcription of the corresponding gene[J]. Immunol Lett ,2004,94 (1-2) :115~122. 被引量:1
  • 8Borges E, Tietz W, Steegmaier W, et al. P-selectin glyc oprotein ligand-1(PSGL-1)on T helper 1 but not on T helper 2 cells binds to P-selectin and supports migration into inflamed skin[J]. J Exp Med, 1997,185 (3) :573~578. 被引量:1
  • 9Li B Q, Bassoro J, Rossman M D et al. Involvement of the Fas/Fas ligand pathway in activated-induced cell death of the mycobacteria-reactive γδT cells in patients with pulmonary tuberculosis[J].J Immunol,1998;161:1558-1562. 被引量:1
  • 10Zingoni A,Palmieri G,Morrone S et al. CD69-triggered ERK activation and functions are negatively regulated by CD94 /NKG2-A inhibitory receptor[J]. Eur J Immunol,2000;30(2):644-650. 被引量:1

共引文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部