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The functional and pathologic relevance of autophagy proteases.自噬蛋白酶的功能及病理相关性。
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本文引用的文献

1
Exosomes and autophagy: coordinated mechanisms for the maintenance of cellular fitness.外泌体和自噬:维持细胞健康的协调机制。
Front Immunol. 2014 Aug 20;5:403. doi: 10.3389/fimmu.2014.00403. eCollection 2014.
2
Autophagy and human disease: emerging themes.自噬与人类疾病:新出现的主题。
Curr Opin Genet Dev. 2014 Jun;26:16-23. doi: 10.1016/j.gde.2014.04.003. Epub 2014 Jun 5.
3
The mitochondrial deubiquitinase USP30 opposes parkin-mediated mitophagy.线粒体去泛素化酶 USP30 拮抗 parkin 介导的线粒体自噬。
Nature. 2014 Jun 19;510(7505):370-5. doi: 10.1038/nature13418. Epub 2014 Jun 4.
4
The deubiquitinase USP15 antagonizes Parkin-mediated mitochondrial ubiquitination and mitophagy.去泛素化酶USP15拮抗Parkin介导的线粒体泛素化和线粒体自噬。
Hum Mol Genet. 2014 Oct 1;23(19):5227-42. doi: 10.1093/hmg/ddu244. Epub 2014 May 22.
5
ARHI (DIRAS3) induces autophagy in ovarian cancer cells by downregulating the epidermal growth factor receptor, inhibiting PI3K and Ras/MAP signaling and activating the FOXo3a-mediated induction of Rab7.ARHI(DIRAS3)通过下调表皮生长因子受体、抑制PI3K和Ras/MAP信号传导以及激活FOXo3a介导的Rab7诱导,从而在卵巢癌细胞中诱导自噬。
Cell Death Differ. 2014 Aug;21(8):1275-89. doi: 10.1038/cdd.2014.48. Epub 2014 Apr 25.
6
The core autophagy protein ATG4B is a potential biomarker and therapeutic target in CML stem/progenitor cells.核心自噬蛋白 ATG4B 是 CML 干细胞/祖细胞中的一个潜在生物标志物和治疗靶点。
Blood. 2014 Jun 5;123(23):3622-34. doi: 10.1182/blood-2013-07-516807. Epub 2014 Apr 22.
7
Development of fluorescent substrates and assays for the key autophagy-related cysteine protease enzyme, ATG4B.关键自噬相关半胱氨酸蛋白酶ATG4B荧光底物及检测方法的开发。
Assay Drug Dev Technol. 2014 Apr;12(3):176-89. doi: 10.1089/adt.2013.561.
8
Atomistic autophagy: the structures of cellular self-digestion.原子自噬:细胞自我消化的结构。
Cell. 2014 Apr 10;157(2):300-311. doi: 10.1016/j.cell.2014.01.070.
9
To be or not to be? How selective autophagy and cell death govern cell fate.生还是死?选择性自噬和细胞死亡如何控制细胞命运。
Cell. 2014 Mar 27;157(1):65-75. doi: 10.1016/j.cell.2014.02.049.
10
Neutral lipid stores and lipase PNPLA5 contribute to autophagosome biogenesis.中性脂质储存和脂肪酶 PNPLA5 有助于自噬体的生物发生。
Curr Biol. 2014 Mar 17;24(6):609-20. doi: 10.1016/j.cub.2014.02.008. Epub 2014 Mar 6.

自噬蛋白酶的功能及病理相关性。

The functional and pathologic relevance of autophagy proteases.

作者信息

Fernández Álvaro F, López-Otín Carlos

出版信息

J Clin Invest. 2015 Jan;125(1):33-41. doi: 10.1172/JCI73940. Epub 2015 Jan 2.

DOI:10.1172/JCI73940
PMID:25654548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4382236/
Abstract

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.

摘要

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。