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[特发性血小板减少性紫癜患者外周血T淋巴细胞中Fas-FasL和半胱天冬酶-3信号转导通路与细胞凋亡]

[Fas-FasL and caspase-3 signal transduction pathway and apoptosis of peripheral T lymphocytes in ITP patients].

作者信息

Zhong Yong-Gen, Feng Wei-Ying, Luo Hong-Qiang, Fu Jia-Ping, Jin Jie

机构信息

Department of Hematology, Shaoxing People's Hospital, Shaoxing 312000, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2008 May;29(5):329-32.

PMID:18844072
Abstract

OBJECTIVE

To explore the relationship between Fas-FasL-mediated signal transduction pathway and apoptosis of T lymphocyte subset in ITP patients.

METHODS

The expression rates of membrane Fas, FasL and intracellular activated caspase-3 in peripheral T lymphocyte subset were determined by flow cytometry. T cell subsets with caspase-3 protein expression were detected by Western blot.

RESULTS

As compared with that in healthy control group [(29.4 +/- 8.2)%], the expression rate of membrane Fas on CD4+ T cells was significantly increased in ITP patients [(42.1 +/- 9.5)%] (P < 0.05), however, that on CD8+ T cells was only slightly increased [(9.3 +/- 6.0)% vs (13.4 +/- 5.8)%] with no statistical significance (P > 0.05). The expression rate of FasL on T cell subset in ITP patients was significantly increased (P < 0.05), and that of intracellular activated caspase-3 in T cell subset in ITP patients was notably higher than that in healthy control group (P < 0.05). Western blot analysis showed that the expression of pro-caspase-3 and cleaved-caspase-3 in CD4+ T cells in patients with ITP after treatment were significantly reduced compared with those before treatment (P < 0.05).

CONCLUSION

Apoptosis of T lymphocyte subset in ITP patients is accelerated. It is possible that Fas-FasL signal transduction pathway plays an important role in the induction of the apoptosis. The degree of apoptosis of T lymphocytes closely correlates with the disease's activity in ITP patients. Hormone therapy may interfere with Fas-FasL signal transduction pathway of apoptosis.

摘要

目的

探讨特发性血小板减少性紫癜(ITP)患者中Fas-FasL介导的信号转导通路与T淋巴细胞亚群凋亡之间的关系。

方法

采用流式细胞术检测外周血T淋巴细胞亚群中膜Fas、FasL及细胞内活化的半胱天冬酶-3的表达率。用蛋白质印迹法检测有半胱天冬酶-3蛋白表达的T细胞亚群。

结果

与健康对照组[(29.4±8.2)%]相比,ITP患者CD4⁺T细胞上膜Fas的表达率显著升高[(42.1±9.5)%](P<0.05),而CD8⁺T细胞上膜Fas的表达率仅略有升高[(9.3±6.0)%对(13.4±5.8)%],无统计学意义(P>0.05)。ITP患者T细胞亚群上FasL的表达率显著升高(P<0.05),且ITP患者T细胞亚群中细胞内活化的半胱天冬酶-3的表达率明显高于健康对照组(P<0.05)。蛋白质印迹分析显示,ITP患者治疗后CD4⁺T细胞中前半胱天冬酶-3和裂解的半胱天冬酶-3的表达与治疗前相比显著降低(P<0.05)。

结论

ITP患者T淋巴细胞亚群凋亡加速。Fas-FasL信号转导通路可能在诱导凋亡中起重要作用。ITP患者T淋巴细胞凋亡程度与疾病活动度密切相关。激素治疗可能干扰凋亡的Fas-FasL信号转导通路。

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