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溶酶体在心脏肌原纤维和非肌原纤维蛋白降解中的作用。

The role of lysosomes in the degradation of myofibrillar and non-myofibrillar proteins in heart.

作者信息

Wildenthal K, Wakeland J R

出版信息

Prog Clin Biol Res. 1985;180:511-20.

PMID:3898115
Abstract

Lysosomes are presumed to be involved in protein degradation in heart, but their exact role is poorly understood. Several interventions that are known to alter cardiac proteolysis (e.g., insulin) also produce lysosomal changes that might account for the observed changes in protein degradation; but many other interventions appear not to do so. Agents that interfere with lysosomal function (e.g., sucrose, chloroquine, methyladenine, leupeptin) cause a 25% reduction in the rate of degradation of total protein in fetal mouse hearts in organ culture; however, in the same hearts the rate of degradation of myosin and other myofibrillar proteins remains unchanged. Thus, it appears that lysosomes are involved in cardiac proteolysis, but may not play a rate-limiting or regulatory role in many circumstances. The regulation of proteolysis by insulin appears to involve non-lysosomal pathways in addition to any lysosomal alterations it may cause. Furthermore, the initial cleavage of myofibrillar proteins appears no to be dependent on normal lysosomal function.

摘要

溶酶体被认为参与心脏中的蛋白质降解,但其确切作用尚不清楚。已知几种能改变心脏蛋白水解的干预措施(如胰岛素)也会引起溶酶体变化,这可能解释了观察到的蛋白质降解变化;但许多其他干预措施似乎并非如此。干扰溶酶体功能的物质(如蔗糖、氯喹、甲基腺嘌呤、亮抑酶肽)会使器官培养的胎鼠心脏中总蛋白降解速率降低25%;然而,在同一心脏中,肌球蛋白和其他肌原纤维蛋白的降解速率保持不变。因此,看来溶酶体参与心脏蛋白水解,但在许多情况下可能不发挥限速或调节作用。胰岛素对蛋白水解的调节似乎除了可能引起的任何溶酶体改变外,还涉及非溶酶体途径。此外,肌原纤维蛋白的初始切割似乎不依赖于正常的溶酶体功能。

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