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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

Targeting autophagy in cancer

TL;DR: A way forward is suggested for the effective targeting of autophagy by understanding the context-dependent roles of autophile and by capitalizing on modern approaches to clinical trial design.
Journal ArticleDOI

Cargo recognition and degradation by selective autophagy

TL;DR: Different types of selective autophagy are discussed, emphasizing the role of ligand receptors and scaffold proteins in providing cargo specificity, and unanswered questions in the field are highlighted.
Journal ArticleDOI

Targeting autophagy in cancer

TL;DR: Fundamental advances in the biology of autophagy are presented, approaches to targeting Autophagy, the preclinical rationale and clinical experience with hydroxychloroquine in cancer clinical trials, the potential role ofAutophagy in tumor immunity, and recent developments in next‐generation autophagic inhibitors that have clinical potential are presented.
Journal ArticleDOI

Autophagy and Tumor Metabolism

TL;DR: The diverse metabolic fuel sources that can be produced by autophagy provide tumors with metabolic plasticity and can allow them to thrive in what can be an austere microenvironment, and understanding how autophile can fuel cellular metabolism will enable more effective combinatorial therapeutic strategies.
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Cellular adaptation to hypoxia through hypoxia inducible factors and beyond.

TL;DR: Understanding these processes could shed light on pathologies associated with hypoxia, including cardiovascular diseases and cancer, and disease mechanisms, such as inflammation and wound repair.
References
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Journal ArticleDOI

Two MAPK-signaling pathways are required for mitophagy in Saccharomyces cerevisiae

TL;DR: The MAP kinase Slt2 is required for both mitophagy and pexophagy, whereas the MAP kinases Hog1 and Hog1 acts specifically inMitophagy.
Journal ArticleDOI

Two-Site Recognition of Phosphatidylinositol 3-Phosphate by PROPPINs in Autophagy

TL;DR: The crystal structure of the yeast PROPPIN Hsv2 is reported, which consists of a seven-bladed β-propeller and, unexpectedly, contains two pseudo-equivalent PI(3)P binding sites on blades 5 and 6, which provide a structural and mechanistic framework for one of the conserved central molecular recognition events in autophagy.
Journal ArticleDOI

Chemical genetic analysis of Apg1 reveals a non-kinase role in the induction of autophagy.

TL;DR: It is found that Apg1 kinase activity is required only for Cvt trafficking of aminopeptidase I but not for import via autophagy, and the data support a novel role for ApG1 in nucleation of autophagosomes that is distinct from its catalytic kinases activity and imply a qualitative difference in the mechanism of autophile formation.
Journal ArticleDOI

Aminopeptidase I is targeted to the vacuole by a nonclassical vesicular mechanism.

TL;DR: Immunogold EM confirms that prAPI is localized in cytosolic and in subvacuolar vesicles in a mutant strain defective in autophagic body degradation, and data suggest that cytosols containing prAPI fuse with the vacuole to release a membrane-bounded intermediate compartment that is subsequently broken down, allowing API maturation.
Journal ArticleDOI

Crystal structure and biochemical analyses reveal Beclin 1 as a novel membrane binding protein

TL;DR: The crystal structure of the evolutionarily conserved domain (ECD) of Beclin 1 at 1.6 Å resolution is reported, which exhibits a previously unreported fold and defines a novel class of membrane-binding domain, with a strong preference for lipid membrane enriched with cardiolipin.
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