40
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Autophagy in the presynaptic compartment in health and disease

      review-article
      1 , 2 , 3 , , 1 , 2 , 3 ,
      The Journal of Cell Biology
      The Rockefeller University Press

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Vijayan and Verstreken review the process of autophagy in the synapse and the role of autophagy in maintaining neuronal function.

          Abstract

          Synapses are functionally distinct neuronal compartments that are critical for brain function, with synaptic dysfunction being an early pathological feature in aging and disease. Given the large number of proteins needed for synaptic function, the proliferation of defective proteins and the subsequent loss of protein homeostasis may be a leading cause of synaptic dysfunction. Autophagic mechanisms are cellular digestion processes that recycle cellular components and contribute to protein homeostasis. Autophagy is important within the nervous system, but its function in specific compartments such as the synapse has been unclear. Evidence from research on both autophagy and synaptic function suggests that there are links between the two and that synaptic homeostasis during aging requires autophagy to regulate protein homeostasis. Exciting new work on autophagy-modulating proteins that are enriched at the synapse has begun to link autophagy to synapses and synaptic dysfunction in disease. A better understanding of these links will help us harness the potential therapeutic benefits of autophagy in combating age-related disorders of the nervous system.

          Related collections

          Most cited references89

          • Record: found
          • Abstract: found
          • Article: not found

          Loss of the autophagy protein Atg16L1 enhances endotoxin-induced IL-1beta production.

          Systems for protein degradation are essential for tight control of the inflammatory immune response. Autophagy, a bulk degradation system that delivers cytoplasmic constituents into autolysosomes, controls degradation of long-lived proteins, insoluble protein aggregates and invading microbes, and is suggested to be involved in the regulation of inflammation. However, the mechanism underlying the regulation of inflammatory response by autophagy is poorly understood. Here we show that Atg16L1 (autophagy-related 16-like 1), which is implicated in Crohn's disease, regulates endotoxin-induced inflammasome activation in mice. Atg16L1-deficiency disrupts the recruitment of the Atg12-Atg5 conjugate to the isolation membrane, resulting in a loss of microtubule-associated protein 1 light chain 3 (LC3) conjugation to phosphatidylethanolamine. Consequently, both autophagosome formation and degradation of long-lived proteins are severely impaired in Atg16L1-deficient cells. Following stimulation with lipopolysaccharide, a ligand for Toll-like receptor 4 (refs 8, 9), Atg16L1-deficient macrophages produce high amounts of the inflammatory cytokines IL-1beta and IL-18. In lipopolysaccharide-stimulated macrophages, Atg16L1-deficiency causes Toll/IL-1 receptor domain-containing adaptor inducing IFN-beta (TRIF)-dependent activation of caspase-1, leading to increased production of IL-1beta. Mice lacking Atg16L1 in haematopoietic cells are highly susceptible to dextran sulphate sodium-induced acute colitis, which is alleviated by injection of anti-IL-1beta and IL-18 antibodies, indicating the importance of Atg16L1 in the suppression of intestinal inflammation. These results demonstrate that Atg16L1 is an essential component of the autophagic machinery responsible for control of the endotoxin-induced inflammatory immune response.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Neural mechanisms of ageing and cognitive decline.

            During the past century, treatments for the diseases of youth and middle age have helped raise life expectancy significantly. However, cognitive decline has emerged as one of the greatest health threats of old age, with nearly 50% of adults over the age of 85 afflicted with Alzheimer's disease. Developing therapeutic interventions for such conditions demands a greater understanding of the processes underlying normal and pathological brain ageing. Recent advances in the biology of ageing in model organisms, together with molecular and systems-level studies of the brain, are beginning to shed light on these mechanisms and their potential roles in cognitive decline.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Mammalian Autophagy: How Does It Work?

              Autophagy is a conserved intracellular pathway that delivers cytoplasmic contents to lysosomes for degradation via double-membrane autophagosomes. Autophagy substrates include organelles such as mitochondria, aggregate-prone proteins that cause neurodegeneration and various pathogens. Thus, this pathway appears to be relevant to the pathogenesis of diverse diseases, and its modulation may have therapeutic value. Here, we focus on the cell and molecular biology of mammalian autophagy and review the key proteins that regulate the process by discussing their roles and how these may be modulated by posttranslational modifications. We consider the membrane-trafficking events that impact autophagy and the questions relating to the sources of autophagosome membrane(s). Finally, we discuss data from structural studies and some of the insights these have provided.
                Bookmark

                Author and article information

                Journal
                J Cell Biol
                J. Cell Biol
                jcb
                jcb
                The Journal of Cell Biology
                The Rockefeller University Press
                0021-9525
                1540-8140
                03 July 2017
                : 216
                : 7
                : 1895-1906
                Affiliations
                [1 ]Department of Neurosciences, Katholieke University Leuven, 3000 Leuven, Belgium
                [2 ]Leuven Institute for Neurodegenerative Disease, Katholieke University Leuven, 3000 Leuven, Belgium
                [3 ]VIB Center for Brain and Disease Research, 3000 Leuven, Belgium
                Author notes
                Correspondence to Vinoy Vijayan: vinoy.vijayan@ 123456kuleuven.vib.be ;
                Patrik Verstreken: patrik.verstreken@kuleuven.vib.be
                Author information
                http://orcid.org/0000-0002-7730-1405
                http://orcid.org/0000-0002-5073-5393
                Article
                201611113
                10.1083/jcb.201611113
                5496617
                28515275
                4f952cfe-a044-4004-ad9a-aad408770cf3
                © 2017 Vijayan and Verstreken

                This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).

                History
                : 23 December 2016
                : 30 March 2017
                : 25 April 2017
                Funding
                Funded by: KU Leuven, DOI http://dx.doi.org/10.13039/501100004040;
                Funded by: European Research Council, DOI http://dx.doi.org/10.13039/100010663;
                Funded by: Fonds Wetenschappelijk Onderzoek, DOI http://dx.doi.org/10.13039/501100003130;
                Funded by: Federaal Wetenschapsbeleid, DOI http://dx.doi.org/10.13039/501100002749;
                Funded by: VIB, DOI http://dx.doi.org/10.13039/501100004727;
                Categories
                Reviews
                Review
                33
                43

                Cell biology
                Cell biology

                Comments

                Comment on this article