摘要
本研究采用双色免疫荧光染色技术,用流式细胞计观察了经E花环法分离的正常人外周血T细胞和经补体介导的细胞毒方法用OKT8单克隆抗体分离的人外周血CD4+细胞在佛波酯(PMA,一种PKC激酶活化剂)活化早期细胞表型的变化情况。我们已经研究了PMA对人胎儿胸腺细胞表型变化的影响,发现PMA可明显下调胸腺DP亚群CD4、CD8和CD3分子表达。但能明显促进CD25和HLA-Ⅰ类抗原表达。本文旨在通过研究PMA对人外周血T细胞和CD4+亚群表型变化的影响,探讨PMA对发育成熟的外周血T细胞是否发挥同样的调节作用。并且通过观察外周血T细胞和CD4+亚群对PMA的反应性,探讨T细胞在对抗原发生应答而活化时,T细胞亚群之间是否存在某种影响细胞表型变化的相互作用。我们发现PMA同样可下调外周血T细胞CD3CD4和CD8分子的表达,并促进CD25分子表达。PMA对外周血T细胞的作用与胎儿胸腺细胞相比在作用时间上有明显不同。表明处于不同发育阶段的T细胞对pMA表现不同的反应性。另外,外周血总T细胞和CD4+亚群细胞也对PMA表现不同反应性,提示T细胞在PMA作用下发生表型改变时,细胞亚群之间可能存在某种影响细胞表型变化的相互作用?
With double fluorescent-staining and
flowcytometry. we studied the phenotype variation of T cells purifiedfrom PBL with rosette
method and CD4 positive subset purified from rosette T cells with corn plement mediated
cy-totoxicity to delete CD8+ T cells. The purified T cells were cultured with PMA for different
times(0.5,3 ,6 and 12hours);We found that PMA could induce down-modulation of both CD4 and
CD8 expression on mature T cells inPBL.Compared with that of human fetal thymocytes
stimulated with PM A. however,there was obvious difference. The results suggest that T cells on
different differentiation stages may have different responses to PMA. On theother hand,we
found that the phenotypic variation between T cells and CD 4 positive subset cells in PBL had
differ-ent responses to PMA. That means the variation of T cell phenotype may be affected by
interaction of T cell sub-sets as well as be affected by PM A.It may be a very important
modulation existing in T cells activation.We also found that CPZ (Chlorpromazine )which is a
Ca++inhibitor,H7[1-(5-isoquinoline sulfonyl)-2-methylpiperrazine dihydrochloride] which is a
PKC inhibitor ,and EGT A could obviously inhibit downmodulation ofthe expression of CD3,CD4,
CD8 and CD25 by PMA.These results indicate that the flux of Ca++in T cells mayplay an
important action on differentiation and activation of T cell duing early activation。
出处
《中华微生物学和免疫学杂志》
CAS
CSCD
北大核心
1994年第3期176-179,共4页
Chinese Journal of Microbiology and Immunology
关键词
T细胞
表型分化
PMA
Tlympbocyte
Phenotypic Differentiation
PMA