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从口腔癌患者血清中分离出的Fas配体阳性膜性囊泡可诱导活化T淋巴细胞凋亡。

Fas ligand-positive membranous vesicles isolated from sera of patients with oral cancer induce apoptosis of activated T lymphocytes.

作者信息

Kim Jeong Whun, Wieckowski Eva, Taylor Douglas D, Reichert Torsten E, Watkins Simon, Whiteside Theresa L

机构信息

University of Pittsburgh Cancer Institute, Hillman Cancer Center, 5117 Centre Avenue, Pittsburgh, PA 15213, USA.

出版信息

Clin Cancer Res. 2005 Feb 1;11(3):1010-20.

PMID:15709166
Abstract

OBJECTIVE

In patients with oral squamous cell carcinoma, a high proportion of T cells in the tumor undergo apoptosis, which correlates with Fas ligand (FasL) expression on tumor cells. The present study was done to identify mechanisms responsible for apoptosis of T cells seen in the peripheral circulation of these patients.

METHODS

Sera of 27 patients, normal donor sera, and supernatants of cultured normal or tumor cells were fractionated by size exclusion chromatography and ultracentrifugation to isolate microvesicles. The presence of microvesicle-associated FasL was studied by Western blots, blocking with anti-Fas reagents, and immunoelectron microscopy. Biological activities of microvesicles were tested including the ability to induce apoptosis of Jurkat and T-cell blasts. Semiquantitative analysis of FasL in microvesicles was correlated with caspase-3 activity, DNA fragmentation, cytochrome c release, loss of mitochondrial membrane potential, and TCR-zeta chain expression in lymphocytes.

RESULTS

FasL-positive (FasL+) microvesicles were detected in sera of 21 of 27 patients. Microvesicles contained 42 kDa FasL. These microvesicles induced caspase-3 cleavage, cytochrome c release, loss of mitochondrial membrane potential, and reduced TCR-zeta chain expression in target lymphocytes. Biological activity of the FasL+ microvesicles was partially blocked by ZB4 anti-Fas monoclonal antibody. Microvesicle-associated FasL levels correlated with the patients' tumor burden and nodal involvement.

CONCLUSION

Sera of patients with active oral squamous cell carcinoma contain FasL+ microvesicles, which induce the receptor and mitochondrial apoptotic pathways in Jurkat and activated T cells.

摘要

目的

在口腔鳞状细胞癌患者中,肿瘤内高比例的T细胞发生凋亡,这与肿瘤细胞上Fas配体(FasL)的表达相关。本研究旨在确定这些患者外周血循环中T细胞凋亡的机制。

方法

对27例患者的血清、正常供体血清以及培养的正常或肿瘤细胞的上清液进行尺寸排阻色谱和超速离心分离微泡。通过蛋白质免疫印迹、抗Fas试剂阻断和免疫电子显微镜研究微泡相关FasL的存在情况。测试微泡的生物学活性,包括诱导Jurkat细胞和T细胞母细胞凋亡的能力。对微泡中FasL进行半定量分析,并与淋巴细胞中caspase-3活性、DNA片段化、细胞色素c释放、线粒体膜电位丧失和TCR-ζ链表达进行相关性分析。

结果

在27例患者中的21例血清中检测到FasL阳性(FasL+)微泡。微泡含有42 kDa的FasL。这些微泡诱导靶淋巴细胞中caspase-3裂解、细胞色素c释放、线粒体膜电位丧失并降低TCR-ζ链表达。FasL+微泡的生物学活性被ZB4抗Fas单克隆抗体部分阻断。微泡相关FasL水平与患者的肿瘤负荷和淋巴结受累情况相关。

结论

活跃期口腔鳞状细胞癌患者的血清中含有FasL+微泡,其可诱导Jurkat细胞和活化T细胞中的受体和线粒体凋亡途径。

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