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Terfenadine induces thymocyte apoptosis via mitochondrial pathway.

机译:特非那定通过线粒体途径诱导胸腺细胞凋亡。

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The treatment of rat thymocytes with 10 microM terfenadine resulted in a significant increase in DNA fragmentation. The DNA fragmentation induced by terfenadine was dependent on its concentration and incubation time. In terfenadine-treated cells, the translocation of phosphatidylserine from the inside of plasma membrane to the outside, an early event of the apoptotic process, and chromatin condensation, the morphological characterization of apoptotic cell death, were observed. Terfenadine stimulated caspase-8, -9 and -3-like activities in an incubation time-dependent manner in thymocytes. The active forms of caspase-3 and -9 were detected in the extract from terfenadine-treated cells by immunoblotting analysis using specific antibodies to caspases, but active caspase-8 was not found in this fraction. Decrease in mitochondrial membrane potential and the release of cytochrome c from mitochondria to cytosol were observed in terfenadine-treated thymocytes. These results suggest that terfenadine induces apoptosis in rat thymocytes via mitochondrial pathway.
机译:用10 microM terfenadine处理大鼠胸腺细胞会导致DNA片段的显着增加。特非那定诱导的DNA片段化取决于其浓度和孵育时间。在特非那定处理的细胞中,观察到磷脂酰丝氨酸从质膜内部向外部的迁移,这是凋亡过程的早期事件,染色质浓缩是凋亡细胞死亡的形态特征。特非那定在胸腺细胞中以时间依赖性的方式刺激了caspase-8,-9和-3-样活性。使用针对胱天蛋白酶的特异性抗体通过免疫印迹分析从特非那定处理过的细胞的提取物中检测到caspase-3和-9的活性形式,但在该级分中未发现有活性的caspase-8。特非那定处理过的胸腺细胞中线粒体膜电位降低,细胞色素c从线粒体释放到细胞质中。这些结果表明特非那定通过线粒体途径诱导大鼠胸腺细胞凋亡。

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