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没食子酸诱导骨肉瘤 MG-63 细胞中线粒体和半胱氨酸天冬氨酸蛋白酶依赖性细胞凋亡。

Corosolic acid triggers mitochondria and caspase-dependent apoptotic cell death in osteosarcoma MG-63 cells.

机构信息

Department of Orthopedics, Shanghai Tenth People's Hospital, Shanghai, 200072, China.

出版信息

Phytother Res. 2011 Sep;25(9):1354-61. doi: 10.1002/ptr.3422. Epub 2011 Feb 21.

Abstract

The response of osteosarcoma MG-63 cells to corosolic acid treatment has been investigated. The results showed that corosolic acid significantly inhibited cell viability in both a dose and a time dependent manner. It was found that corosolic acid increased the Bax/Bcl-2 ratio by up-regulating Bax expression, disrupted mitochondrial membrane potential and triggered the release of cytochrome c from mitochondria into the cytoplasm. Corosolic acid treatment triggered the activation of caspase-8, 9 and 3. The apoptosis was obviously inhibited by pretreatment with a general caspase inhibitor, z-VAD-FMK. Moreover, pretreatment of CsA, a cyclophilin D ligand that inhibits mitochondria potential uncoupling, prevented the activation of caspase-9 and caspase-3, but not caspase-8, and the apoptosis of MG-63 cells, triggered by corosolic acid. All these results indicated that corosolic acid-induced apoptosis was associated with the activation of caspases via a mitochondrial pathway.

摘要

已经研究了熊果酸处理对骨肉瘤 MG-63 细胞的反应。结果表明,熊果酸以剂量和时间依赖的方式显著抑制细胞活力。发现熊果酸通过上调 Bax 表达增加 Bax/Bcl-2 比值,破坏线粒体膜电位并触发细胞色素 c 从线粒体释放到细胞质中。熊果酸处理触发了 caspase-8、9 和 3 的激活。用通用半胱天冬酶抑制剂 z-VAD-FMK 预处理可明显抑制细胞凋亡。此外,预先用环孢菌素 A(一种抑制线粒体解偶联的亲环蛋白 D 配体)处理可防止 caspase-9 和 caspase-3 的激活,但不能防止 caspase-8 的激活,并且可防止熊果酸诱导的 MG-63 细胞凋亡。所有这些结果表明,熊果酸诱导的细胞凋亡与通过线粒体途径激活半胱天冬酶有关。

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