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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.
Journal ArticleDOI

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

Atg27 is required for autophagy-dependent cycling of Atg9.

TL;DR: A second transmembrane protein Atg27 is required for Atg9 cycling and shuttles between the pre-autophagosomal structure, mitochondria, and the Golgi complex, which support a hypothesis that multiple membrane sources supply the lipids needed for autophagosome formation.
Journal ArticleDOI

Structural and functional characterization of the two phosphoinositide binding sites of PROPPINs, a β-propeller protein family

TL;DR: This work presents the 3.0-Å crystal structure of Kluyveromyces lactis Hsv2, which shares significant sequence homologies with its three Saccharomyces cerevisiae homologs Atg18, Atg21, and Hsv1, and proposes a model for phosphoinositide binding of PROPPINs.
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Endothelial nitric-oxide synthase antisense (NOS3AS) gene encodes an autophagy-related protein (APG9-like2) highly expressed in trophoblast.

TL;DR: These results, taken together with those of phylogenetic and sequence analyses, suggest that both APG9L1 and APG 9L2 are functionally orthologous to the yATG9 in autophagosome formation.
Journal ArticleDOI

Structural basis of Atg8 activation by a homodimeric E1, Atg7.

TL;DR: The structural and biochemical data demonstrate that Atg8 is initially recognized by the C-terminal tail of ECTD and is then transferred to an AD, where the At g8 C terminus is attacked by the catalytic cysteine to form a thioester bond.
Journal ArticleDOI

Analysis of the membrane structures involved in autophagy in yeast by freeze-replica method.

TL;DR: The autophagic body originated from the inner membrane of the Autophagosome, and its membrane reflects an intrinsic feature of autophagosomal membrane, as well as other intracellular organelles.
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