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首页> 外文期刊>American Journal of Physiology >Recent progress in research on molecular mechanisms of autophagy in the heart
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Recent progress in research on molecular mechanisms of autophagy in the heart

机译:心脏自噬分子机制研究进展

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Dysregulation of autophagy, an evolutionarily conserved process for degradation of long-lived proteins and organ-elles, has been implicated in the pathogenesis of human disease. Recent research has uncovered pathways that control autophagy in the heart and molecular mechanisms by which alterations in this process affect cardiac structure and function. Although initially thought to be a nonselective degradation process, autophagy, as it has become increasingly clear, can exhibit specificity in the degradation of molecules and organelles, such as mitochondria. Furthermore, it has been shown that autophagy is involved in a wide variety of previously unrecognized cellular functions, such as cell death and metabolism. A growing body of evidence suggests that deviation from appropriate levels of autophagy causes cellular dysfunction and death, which in turn leads to heart disease. Here, we review recent advances in understanding the role of autophagy in heart disease, highlight unsolved issues, and discuss the therapeutic potential of modulating autophagy in heart disease.
机译:自噬的失调,一种进化的长期蛋白和器官壳的降解过程的进化保护过程,这一切都与人类疾病的发病机制有关。最近的研究已经发现了控制心脏和分子机制中的自噬的途径,通过该过程中的改变影响心脏结构和功能。虽然最初被认为是非选择性的降解过程,但由于它越来越清楚的,患有自噬,可以表现出分子和细胞器的降解的特异性,例如线粒体。此外,已经表明自噬涉及各种先前未被识别的细胞功能,例如细胞死亡和新陈代谢。越来越多的证据表明,偏离适当水平的自噬导致细胞功能障碍和死亡,这反过来导致心脏病。在这里,我们审查最近在理解心脏病中的作用,突出未解决的问题,并讨论在心脏病中调节自噬的治疗潜力。

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