Fernández Álvaro F, López-Otín Carlos
J Clin Invest. 2015 Jan;125(1):33-41. doi: 10.1172/JCI73940. Epub 2015 Jan 2.
Autophagy is a well-conserved catabolic process essential for cellular homeostasis. First described in yeast as an adaptive response to starvation, this pathway is also present in higher eukaryotes, where it is triggered by stress signals such as damaged organelles or pathogen infection. Autophagy is characterized at the cellular level by the engulfment of portions of the cytoplasm in double-membrane structures called autophagosomes. Autophagosomes fuse with lysosomes, resulting in degradation of the inner autophagosomal membrane and luminal content. This process is coordinated by complex molecular systems, including the ATG8 ubiquitin-like conjugation system and the ATG4 cysteine proteases, which are implicated in the formation, elongation, and fusion of these autophagic vesicles. In this Review, we focus on the diverse functional roles of the autophagins, a protease family formed by the four mammalian orthologs of yeast Atg4. We also address the dysfunctional expression of these proteases in several pathologic conditions such as cancer and inflammation and discuss potential therapies based on their modulation.
自噬是一种高度保守的分解代谢过程,对细胞内稳态至关重要。该途径最初在酵母中被描述为对饥饿的适应性反应,在高等真核生物中也存在,在高等真核生物中它由诸如受损细胞器或病原体感染等应激信号触发。自噬在细胞水平上的特征是细胞质的部分被称为自噬体的双膜结构所吞噬。自噬体与溶酶体融合,导致自噬体内膜和腔内内容物降解。这个过程由复杂的分子系统协调,包括ATG8泛素样缀合系统和ATG4半胱氨酸蛋白酶,它们与这些自噬小泡的形成、延长和融合有关。在本综述中,我们重点关注自噬素的多种功能作用,自噬素是由酵母Atg4的四种哺乳动物直系同源物形成的蛋白酶家族。我们还讨论了这些蛋白酶在癌症和炎症等几种病理状况下的功能失调表达,并基于它们的调节作用探讨了潜在的治疗方法。