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首页> 外文期刊>Cytometry: The Journal of the Society for Analytical Cytology >IMPROVED FOUR-COLOR FLOW CYTOMETRY METHOD USING FLUO-3 AND TRIPLE IMMUNOFLUORESCENCE FOR ANALYSIS OF INTRACELLULAR CALCIUM ION ([CA2+]I) FLUXES AMONG MOUSE LYMPH NODE B- AND T-LYMPHOCYTE SUBSETS
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IMPROVED FOUR-COLOR FLOW CYTOMETRY METHOD USING FLUO-3 AND TRIPLE IMMUNOFLUORESCENCE FOR ANALYSIS OF INTRACELLULAR CALCIUM ION ([CA2+]I) FLUXES AMONG MOUSE LYMPH NODE B- AND T-LYMPHOCYTE SUBSETS

机译:改进的四色流式细胞仪,使用FLUO-3和三重免疫荧光法分析小鼠淋巴结B和T淋巴细胞亚群中的细胞内钙离子([CA2 +] I)通量

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摘要

A visible-light, dual-laser, now cytometric method was developed for the simultaneous analysis of intracellular ionized calcium concentration ([Ca2+](i)) and three cell-surface markers (CD4, CD8, and Thy-1.2 antigens) by using the calcium probe fluo-3 and using R-phycoerythrin (PE), peridinin chlorophyll-alpha protein (PerCP), and allophycocyanin (APC) conjugated monoclonal antibodies (MoAbs), This improved method was used in the analysis of [Ca2+](i) mobilization upon in vitro stimulation with mitogenic lectins [phytohaemagglutinin (PHA) or concanavalin A (ConA)], anti-CD3 MoAbs, or A23187 calcium ionophore in the heterogeneous lymph node cell populations from healthy C57BL/Ka mice, The present results show that the calcium responses were heterogeneous and dependent on the cellular immunophenotype, not only on lectins or anti-CD3 MoAbs stimulation, but also on the receptor-independent A23187 ionophore stimulation, An in situ fluo-3 calibration method (using A23187 and metabolic poisons in Ca2+/EGTA buffers with known free calcium concentrations) indicated a resting [Ca2+](i) in lymphocytes of 103 +/- 23 nM (mean +/- S.D.) but with significant differences between the [Ca2+](i) in B cells and in all of the T-cell subsets (CD4+Thy-1(+), CD4(+)Thy-1(-), and CD8(+) T cells), Both the B cells and the T-cell subsets showed an increase of fluo-3 fluorescence upon in vitro stimulation with ConA or PHA, but the calcium mobilization following lectin stimulation was time delayed in all T-cell subsets, Only the T cells, including the CD4(+)Thy-1(-) subset, responded to anti-CD3 MoAbs. The percentage of responding cells upon stimulation with ConA was higher in T cells than in B cells, By contrast, PHA gave a higher response in B cells. After stimulation with different mitogens, [Ca2+](i) increased in both CD4(+) and CD8(+) T-cell subsets, However, the percentage of responding cells was far higher in the CD4(+)Thy-1(+) subset than in the CD4(+)Thy-1(-) or the CD8+ T-cell subsets, The stimulation with A23187 ionophore induced a higher calcium response in B cells than in T cells, Interestingly, it also induced greater Ca2+ mobilization in CD4(+) than in CD8+ T cells, These results demonstrate the potential use of fluo-3 simultaneously with three fluorescein (FITC)-compatible fluorochromes, This technique may be useful for investigating the role of the CD4(+)Thy-1(-) T cells, a rare subset that is abnormally expanded in a murine acquired immunodeficiency syndrome (murine AIDS). (C) 1996 Wiley-Liss, Inc. [References: 54]
机译:开发了一种可见光,双激光,现在细胞计数法,用于同时分析细胞内离子钙浓度([Ca2 +](i))和三种细胞表面标志物(CD4,CD8和Thy-1.2抗原)钙探针fluo-3,并使用R-藻红蛋白(PE),peridinin叶绿素-α蛋白(PerCP)和别藻蓝蛋白(APC)缀合的单克隆抗体(MoAbs),该改进的方法用于分析[Ca2 +](i )在健康C57BL / Ka小鼠的异种淋巴结细胞群体中用有丝分裂凝集素[植物血凝素(PHA)或伴刀豆球蛋白A(ConA)],抗CD3 MoAb或A23187钙离子载体体外刺激时动员,目前的结果表明,钙反应是异质的,不仅依赖于凝集素或抗CD3 MoAbs刺激,还依赖于细胞免疫表型,还依赖于非受体依赖的A23187离子载体刺激,一种原位荧光3校准方法(使用A23187和代谢毒物)已知游离钙浓度的Ca2 + / EGTA缓冲液中的s表示在103 +/- 23 nM(平均值+/- SD)的淋巴细胞中有静止的[Ca2 +](i),但在[Ca2 +](i)之间有显着差异B细胞和所有T细胞亚群(CD4 + Thy-1(+),CD4(+)Thy-1(-)和CD8(+)T细胞)中,B细胞和T细胞亚群显示在ConA或PHA体外刺激后fluo-3荧光增加,但在所有T细胞亚群中凝集素刺激后的钙动员时间延迟,只有T细胞,包括CD4(+)Thy-1( -)亚群,对抗CD3 MoAb产生反应。 T细胞中ConA刺激后应答细胞的百分比高于B细胞。相比之下,PHA在B细胞中给出了更高的应答。在用不同的促分裂原刺激后,[Ca2 +](i)在CD4(+)和CD8(+)T细胞亚群中均增加,但是,响应细胞的百分比在CD4(+)Thy-1(+ )子集比CD4(+)Thy-1(-)或CD8 + T细胞子集更明显,A23187离子载体的刺激在B细胞中引起的钙反应高于T细胞,有趣的是,它还诱导了更大的Ca2 +动员。 CD4(+)比CD8 + T细胞中的这些,这些结果证明了fluo-3与三种与荧光素(FITC)兼容的荧光染料同时使用的潜力。该技术可能对研究CD4(+)Thy-1( -)T细胞,一种罕见的亚群,在小鼠获得性免疫缺陷综合症(鼠类艾滋病)中异常扩增。 (C)1996 Wiley-Liss,Inc. [参考:54]

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