溶酶体和微管在心脏蛋白降解中的作用。

K Wildenthal, J S Crie, J M Ord, J R Wakeland
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引用次数: 3

摘要

心脏蛋白水解的机制和调控因素尚不完全清楚。干扰溶酶体功能的药物(如氯喹、白细胞介素、甲基腺嘌呤)可使蛋白质降解的总速率降低25-30%。然而,在相同的心脏中,肌凝蛋白的分解率保持不变。用秋水仙碱分解微管的同时,总蛋白和肌球蛋白的降解率降低15%。在同样的心脏中,包括线粒体细胞色素在内的“细胞器”蛋白的降解减少了30%以上。因此,似乎不同种类的心脏蛋白的降解可以通过不同的过程来完成和调节。溶酶体在整体蛋白水解中很重要,但似乎不参与肌凝蛋白分解的调节。微管也参与蛋白质水解过程,似乎对线粒体和其他细胞器的蛋白质分解特别重要。
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The role of lysosomes and microtubules in cardiac protein degradation.

The mechanisms and regulatory factors involved in cardiac proteolysis are incompletely understood. Agents that interfere with lysosomal function (e.g., chloroquine, leupeptin, methyladenine) cause a 25-30% reduction in the overall rate of protein degradation. In the same hearts, however, the rate of myosin breakdown remains unchanged. Disaggregation of micro-tubules with colchicine is accompanied by a 15% reduction in the rate of degradation of total protein and of myosin. In the same hearts, the degradation of "organellar" protein, including mitochondrial cytochromes, is reduced by over 30%. Thus, it appears that the degradation of different classes of cardiac proteins may be accomplished and regulated by different processes. Lysosomes are important in overall proteolysis, but appear not to be involved in the regulation of myosin breakdown. Microtubules are also involved in the proteolytic process, and appear to be especially important for the breakdown of proteins from mitochondria and perhaps other organelles.

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