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组织蛋白酶D的抑制可防止自由基诱导的大鼠心肌细胞凋亡。

Inhibition of cathepsin D prevents free-radical-induced apoptosis in rat cardiomyocytes.

作者信息

Ollinger K

机构信息

Faculty of Health Sciences, Link]oping University, Link]oping, S-581 85, Sweden.

出版信息

Arch Biochem Biophys. 2000 Jan 15;373(2):346-51. doi: 10.1006/abbi.1999.1567.

Abstract

Apoptosis was inhibited in rat cardiomyocytes pretreated with the aspartic protease inhibitor pepstatin A and subsequently exposed to naphthazarin (5,8-dihydroxy-1,4-naphthoquinone). Cathepsin D was released from lysosomes to the cytosol upon exposure to naphthazarin, and the enzyme activity decreased simultaneously. Later, cathepsin D reappeared in granules of increased size, and enzyme activity was restored. Activation of caspase-3-like proteases was detected, and the number of cells showing apoptotic morphology increased with time. Pepstatin A pretreatment did not prevent release of cathepsin D from lysosomes but did significantly inhibit subsequent naphthazarin-induced caspase activation and apoptotic morphology. This suggests that cathepsin D exerts its apoptosis-stimulating effect upstream of caspase-3-like activation.

摘要

在用天冬氨酸蛋白酶抑制剂胃蛋白酶抑素A预处理大鼠心肌细胞,随后使其暴露于萘茜(5,8 - 二羟基 - 1,4 - 萘醌)的情况下,细胞凋亡受到抑制。暴露于萘茜后,组织蛋白酶D从溶酶体释放到细胞质中,同时酶活性下降。随后,组织蛋白酶D重新出现在尺寸增大的颗粒中,酶活性得以恢复。检测到半胱天冬酶 - 3样蛋白酶的激活,并且呈现凋亡形态的细胞数量随时间增加。胃蛋白酶抑素A预处理并未阻止组织蛋白酶D从溶酶体的释放,但确实显著抑制了随后萘茜诱导的半胱天冬酶激活和凋亡形态。这表明组织蛋白酶D在半胱天冬酶 - 3样激活的上游发挥其促凋亡作用。

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