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Open AccessJournal ArticleDOI

The machinery of macroautophagy

Yuchen Feng, +3 more
- 01 Jan 2014 - 
- Vol. 24, Iss: 1, pp 24-41
TLDR
This review focuses on macroautophagy, briefly describing the discovery of this process in mammalian cells, discussing the current views concerning the donor membrane that forms the phagophore, and characterizing the autophagy machinery including the available structural information.
Abstract
Autophagy is a primarily degradative pathway that takes place in all eukaryotic cells. It is used for recycling cytoplasm to generate macromolecular building blocks and energy under stress conditions, to remove superfluous and damaged organelles to adapt to changing nutrient conditions and to maintain cellular homeostasis. In addition, autophagy plays a critical role in cytoprotection by preventing the accumulation of toxic proteins and through its action in various aspects of immunity including the elimination of invasive microbes and its participation in antigen presentation. The most prevalent form of autophagy is macroautophagy, and during this process, the cell forms a double-membrane sequestering compartment termed the phagophore, which matures into an autophagosome. Following delivery to the vacuole or lysosome, the cargo is degraded and the resulting macromolecules are released back into the cytosol for reuse. The past two decades have resulted in a tremendous increase with regard to the molecular studies of autophagy being carried out in yeast and other eukaryotes. Part of the surge in interest in this topic is due to the connection of autophagy with a wide range of human pathophysiologies including cancer, myopathies, diabetes and neurodegenerative disease. However, there are still many aspects of autophagy that remain unclear, including the process of phagophore formation, the regulatory mechanisms that control its induction and the function of most of the autophagy-related proteins. In this review, we focus on macroautophagy, briefly describing the discovery of this process in mammalian cells, discussing the current views concerning the donor membrane that forms the phagophore, and characterizing the autophagy machinery including the available structural information.

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Journal ArticleDOI

Autophagy: a housekeeper in cardiorenal metabolic health and disease.

TL;DR: A recent surge in autophagy research is highlighted, such as the cellular quality control through the disposal and recycling of cellular components, and the contemporary understanding of molecular mechanisms of autophile in diverse organ or tissues involved in the pathogenesis of CRS is summarized.
Journal ArticleDOI

Comparative analyses of ubiquitin-like ATG8 and cysteine protease ATG4 autophagy genes in the plant lineage and cross-kingdom processing of ATG8 by ATG4.

TL;DR: Results revealed that the yeast Atg4 processes Arabidopsis ATG8 but not human LC3A (HsLC3A) and Broad ATg8 processing by HsATG4B and lack of processing of HsLC 3A by yeast and plant ATG4s suggest that the cross-kingdom ATG7 processing is determined by ATG9 sequence rather than ATG5, further support the evolutionarily conserved maturation of ATG6.
Journal ArticleDOI

Molecular regulation of autophagy and its implications for metabolic diseases.

TL;DR: Autophagy is an evolutionarily conserved cellular program for the turnover of organelles, proteins, and other macromolecules, involving the lysosomal degradation pathway.
Journal ArticleDOI

Degradation of Organelles or Specific Organelle Components via Selective Autophagy in Plant Cells

TL;DR: In plants, selective autophagy has recently been shown to degrade mitochondria, plastids and peroxisomes, or organelle components such as the endoplasmic-reticulum membrane and chloroplast-derived proteins such as Rubisco, placing selective-autophagy as a major factor in cellular steady-state maintenance, both under stress and favorable environmental conditions.
Journal ArticleDOI

Control of Autophagy in Chlamydomonas Is Mediated through Redox-Dependent Inactivation of the ATG4 Protease.

TL;DR: It is proposed that the activity of the ATG4 protease is finely regulated by the intracellular redox state, and it is inhibited under stress conditions to ensure lipidation of ATG8 and thus autophagy progression in C. reinhardtii.
References
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Journal ArticleDOI

AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1

TL;DR: A molecular mechanism for regulation of the mammalian autophagy-initiating kinase Ulk1, a homologue of yeast ATG1, is demonstrated and a signalling mechanism for UlK1 regulation and autophagic induction in response to nutrient signalling is revealed.
Journal ArticleDOI

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

TL;DR: Mutations in the newly identified gene appear to be responsible for the pathogenesis of Autosomal recessive juvenile parkinsonism, and the protein product is named ‘Parkin’.
Journal ArticleDOI

Tissue fractionation studies. 6. Intracellular distribution patterns of enzymes in rat-liver tissue

TL;DR: The results are shown to favour the ferryl ion structure, or an isomer of this structure, for the higher oxidation state, and theHigher oxidation state may provisionally be named ferrylmyoglobin.
Journal ArticleDOI

Autophagy: process and function

TL;DR: In this review, the process of autophagy is summarized, and the role of autophileagy is discussed in a process-based manner.
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