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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.
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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.
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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

Autophagy modulation as a potential therapeutic target for diverse diseases

TL;DR: An overview of the mechanisms and regulation of autophagy, the role of this pathway in disease and strategies for therapeutic modulation is provided.
Journal ArticleDOI

Regulation of an ATG7-beclin 1 Program of Autophagic Cell Death by Caspase-8

TL;DR: A new molecular pathway in which activation of the receptor-interacting protein (a serine-threonine kinase) and Jun amino-terminal kinase induced cell death with the morphology of autophagy is defined.
Journal ArticleDOI

ULK1 induces autophagy by phosphorylating Beclin-1 and activating VPS34 lipid kinase

TL;DR: A molecular mechanism linking ULK to the pro-autophagic lipid kinase VPS34 is described, whereby the activated ULK1 phosphorylates Beclin-1 on Ser 14, thereby enhancing the activity of the ATG14L-containing V PS34 complexes.
Journal ArticleDOI

Tor-Mediated Induction of Autophagy via an Apg1 Protein Kinase Complex

TL;DR: It is shown that the protein kinase activity of Apg1 is enhanced by starvation or rapamycin treatment, and it is found that Apg13, which binds to and activates ApG1, is hyperphosphorylated in a Tor-dependent manner, reducing its affinity to Apg 1.
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