Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/100130
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dc.contributor.authorRichards, R.-
dc.contributor.authorRobertson, S.-
dc.contributor.authorO'Keefe, L.-
dc.contributor.authorFornarino, D.-
dc.contributor.authorScott, A.-
dc.contributor.authorLardelli, M.-
dc.contributor.authorBaune, B.-
dc.date.issued2016-
dc.identifier.citationFrontiers in Neuroscience, 2016; 10(MAY):193-1-193-20-
dc.identifier.issn1662-4548-
dc.identifier.issn1662-453X-
dc.identifier.urihttp://hdl.handle.net/2440/100130-
dc.description.abstractNeurodegenerative diseases comprise an array of progressive neurological disorders all characterized by the selective death of neurons in the central nervous system. Although, rare (familial) and common (sporadic) forms can occur for the same disease, it is unclear whether this reflects several distinct pathogenic pathways or the convergence of different causes into a common form of nerve cell death. Remarkably, neurodegenerative diseases are increasingly found to be accompanied by activation of the innate immune surveillance system normally associated with pathogen recognition and response. Innate surveillance is the cell's quality control system for the purpose of detecting such danger signals and responding in an appropriate manner. Innate surveillance is an "intelligent system," in that the manner of response is relevant to the magnitude and duration of the threat. If possible, the threat is dealt with within the cell in which it is detected, by degrading the danger signal(s) and restoring homeostasis. If this is not successful then an inflammatory response is instigated that is aimed at restricting the spread of the threat by elevating degradative pathways, sensitizing neighboring cells, and recruiting specialized cell types to the site. If the danger signal persists, then the ultimate response can include not only the programmed cell death of the original cell, but the contents of this dead cell can also bring about the death of adjacent sensitized cells. These responses are clearly aimed at destroying the ability of the detected pathogen to propagate and spread. Innate surveillance comprises intracellular, extracellular, non-cell autonomous and systemic processes. Recent studies have revealed how multiple steps in these processes involve proteins that, through their mutation, have been linked to many familial forms of neurodegenerative disease. This suggests that individuals harboring these mutations may have an amplified response to innate-mediated damage in neural tissues, and renders innate surveillance mediated cell death a plausible common pathogenic pathway responsible for neurodegenerative diseases, in both familial and sporadic forms. Here we have assembled evidence in favor of the hypothesis that neurodegenerative disease is the cumulative result of chronic activation of the innate surveillance pathway, triggered by endogenous or environmental danger or damage associated molecular patterns in a progressively expanding cascade of inflammation, tissue damage and cell death.-
dc.description.statementofresponsibilityRobert I. Richards, Sarah A. Robertson, Louise V. O’Keefe, Dani Fornarino, Andrew Scott, Michael Lardelli, and Bernhard T. Baune-
dc.language.isoen-
dc.publisherFrontiers Media SA-
dc.rightsCopyright © 2016 Richards, Robertson, O’Keefe, Fornarino, Scott, Lardelli and Baune. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.-
dc.source.urihttp://dx.doi.org/10.3389/fnins.2016.00193-
dc.subjectDementia; innate autoimmunity; inflammation; neurodegeneration; Alzheimer’s, Parkinson’s, Huntington’s-
dc.titleThe enemy within: innate surveillance-mediated cell death, the common mechanism of neurodegenerative disease-
dc.typeJournal article-
dc.identifier.doi10.3389/fnins.2016.00193-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1069348-
pubs.publication-statusPublished-
dc.identifier.orcidRobertson, S. [0000-0002-9967-0084]-
dc.identifier.orcidLardelli, M. [0000-0002-4289-444X]-
dc.identifier.orcidBaune, B. [0000-0001-6548-426X]-
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Molecular and Biomedical Science publications

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