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醚磷脂ET-18-OCH3诱导人丝裂原激活的外周血T淋巴细胞凋亡:Fas受体/配体系统的参与

Induction of apoptosis in human mitogen-activated peripheral blood T-lymphocytes by the ether phospholipid ET-18-OCH3: involvement of the Fas receptor/ligand system.

作者信息

Cabaner C, Gajate C, Macho A, Muñoz E, Modolell M, Mollinedo F

机构信息

Centro de Investigación del Cáncer, Instituto de Biología Molecular y Celular del Cáncer, CSIC-Universidad de Salamanca, Spain.

出版信息

Br J Pharmacol. 1999 Jun;127(4):813-25. doi: 10.1038/sj.bjp.0702606.

Abstract
  1. Activated T-cells constitute a target for treatment of autoimmune diseases. We have found that the antitumour ether phospholipid 1-O-octadecyl-2-O-methyl-rac-glycero-3-phosphocholine (ET-18-OCH3; edelfosine) induced dose- and time-dependent apoptosis in human mitogen-activated peripheral blood T-lymphocytes, but not in resting T-cells. T-lymphocytes were stimulated with phytohemagglutinin and interleukin-2 or with concanavalin A. Apoptosis was assessed by DNA fragmentation through cell cycle and TUNEL analyses, as well as through visualization of internucleosomal DNA fragmentation in agarose gels. 2. The ET-18-OCH3-mediated apoptotic response in activated T-lymphocytes was less intense than in human leukaemic T cell lines, such as Jurkat cells and Peer cells; namely about 25% apoptosis in activated T-cells versus about 46-61% apoptosis in T leukaemic cells after 24 h treatment with 10 microM ET-18-OCH3. 3. The ET-18-OCH3 thioether analogue BM 41.440 (ilmofosine) showed a similar apoptotic capacity to that found with ET-18-OCH3 in activated T-cells, whereas the phospholipid analogue hexadecylphosphocholine (miltefosine) failed to promote this response. 4. The uptake of [3H]-ET-18-OCH3 was much larger in activated T-cells than in resting lymphocytes. 5. Using a cytofluorimetric approach we have found that ET-18-OCH3 induced disruption of the mitochondrial transmembrane potential and production of reactive oxygen species in activated T-cells, but not in resting lymphocytes. 6. ET-18-OCH3 induced an increase in Fas (APO-1/CD95) ligand mRNA expression in activated T-cells, and incubation with a blocking anti-Fas (APO-1/CD95) antibody partially inhibited the ET-18-OCH3-induced apoptosis of activated T-lymphocytes. 7. These results demonstrate that mitogen-activated T-cells, unlike resting lymphocytes, are able to take up significant amounts of ET-18-OCH3, and are susceptible to undergo apoptosis by the ether lipid via, in part, the Fas (APO-1/CD95) receptor/ligand system. This ET-18-OCH3 apoptotic action can be of importance in the therapeutic action of this ether lipid in certain autoimmune diseases.
摘要
  1. 活化的T细胞是自身免疫性疾病治疗的一个靶点。我们发现抗肿瘤醚磷脂1-O-十八烷基-2-O-甲基-rac-甘油-3-磷酸胆碱(ET-18-OCH3;依地福新)可在人丝裂原激活的外周血T淋巴细胞中诱导剂量和时间依赖性的细胞凋亡,但对静息T细胞无此作用。用植物血凝素和白细胞介素-2或伴刀豆球蛋白A刺激T淋巴细胞。通过细胞周期和TUNEL分析检测DNA片段化,以及通过在琼脂糖凝胶中观察核小体间DNA片段化来评估细胞凋亡。2. ET-18-OCH3介导的活化T淋巴细胞凋亡反应不如人白血病T细胞系(如Jurkat细胞和Peer细胞)强烈;即在10μM ET-18-OCH3处理24小时后,活化T细胞中的凋亡率约为25%,而白血病T细胞中的凋亡率约为46%-61%。3. ET-18-OCH3硫醚类似物BM 41.440( ilmofosine)在活化T细胞中显示出与ET-18-OCH3相似的凋亡能力,而磷脂类似物十六烷基磷酸胆碱(米托蒽醌)未能促进这种反应。4. 活化T细胞对[3H]-ET-18-OCH3的摄取量比静息淋巴细胞大得多。5. 使用细胞荧光分析方法,我们发现ET-18-OCH3可诱导活化T细胞中线粒体跨膜电位的破坏和活性氧的产生,但对静息淋巴细胞无此作用。6. ET-18-OCH3可诱导活化T细胞中Fas(APO-1/CD95)配体mRNA表达增加,用阻断性抗Fas(APO-1/CD95)抗体孵育可部分抑制ET-18-OCH3诱导的活化T淋巴细胞凋亡。7. 这些结果表明,与静息淋巴细胞不同,丝裂原激活的T细胞能够摄取大量的ET-18-OCH3,并且部分通过Fas(APO-1/CD95)受体/配体系统易受醚脂诱导的细胞凋亡影响。这种ET-18-OCH3的凋亡作用在该醚脂对某些自身免疫性疾病的治疗作用中可能具有重要意义。

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