Unraveling the complexity of chaperone-mediated autophagy in aging: insights into sex-specific and cell-type-specific regulation.

Rongcan Luo
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引用次数: 0

Abstract

Chaperone-mediated autophagy (CMA) is a selective autophagic pathway that targets specific proteins for lysosomal degradation, playing a crucial role in maintaining cellular homeostasis. Recent research has highlighted the involvement of CMA in aging and age-related diseases, yet its regulation remains complex. The study by Khawaja et al. provides novel insights into the sex-specific and cell-type-specific regulation of CMA during aging. This commentary discusses the key findings of this study, their implications for autophagy and aging research, and potential future directions. Understanding these regulatory mechanisms is essential for developing targeted therapies to combat age-related diseases and promote healthy aging.

揭示老化中伴侣介导的自噬的复杂性:对性别特异性和细胞类型特异性调节的见解。
伴侣蛋白介导的自噬(CMA)是一种选择性自噬途径,针对特定蛋白进行溶酶体降解,在维持细胞稳态中起着至关重要的作用。最近的研究强调了CMA在衰老和年龄相关疾病中的作用,但其调控仍然很复杂。Khawaja等人的研究为衰老过程中CMA的性别特异性和细胞类型特异性调控提供了新的见解。本文讨论了本研究的主要发现,它们对自噬和衰老研究的意义,以及潜在的未来方向。了解这些调节机制对于开发靶向治疗以对抗年龄相关疾病和促进健康老龄化至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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