Systemic inflammation switches the inflammatory cytokine profile in CNS Wallerian degeneration
Axon loss in the CNS is characteristic of many neurodegenerative diseases but the mechanisms of axon degeneration are poorly understood. In particular, we know little of the inflammatory response triggered by CNS axon degeneration with comparison to that provoked by death of the neuronal cell body....
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doaj-7fd638a8361941059f3ac1e2fea5ce212021-03-20T04:55:19ZengElsevierNeurobiology of Disease1095-953X2008-04-013011929Systemic inflammation switches the inflammatory cytokine profile in CNS Wallerian degenerationKarine Palin0Colm Cunningham1Penny Forse2V. Hugh Perry3Nick Platt4CNS Inflammation Group, School of Biological Sciences, University of Southampton, Southampton SO16 7PX, UKCNS Inflammation Group, School of Biological Sciences, University of Southampton, Southampton SO16 7PX, UKCNS Inflammation Group, School of Biological Sciences, University of Southampton, Southampton SO16 7PX, UKCNS Inflammation Group, School of Biological Sciences, University of Southampton, Southampton SO16 7PX, UKCorresponding author. Fax: +44 2380 592711.; CNS Inflammation Group, School of Biological Sciences, University of Southampton, Southampton SO16 7PX, UKAxon loss in the CNS is characteristic of many neurodegenerative diseases but the mechanisms of axon degeneration are poorly understood. In particular, we know little of the inflammatory response triggered by CNS axon degeneration with comparison to that provoked by death of the neuronal cell body. We show that Wallerian degeneration of the mouse optic nerve induces transcription of TGF-β1 and TNF-α, but not pro-inflammatory cytokines IL-1β and IL-6 and microglial activation. This atypical inflammatory response resembles macrophages that have phagocytosed apoptotic cells and prion-infected CNS. Significantly, peripheral endotoxin challenge after injury switched this profile by inducing IL-1β, IL-6 transcripts, other inflammation-associated products and reducing neurofilament immunoreactivity. We propose that microglia are activated by Wallerian degeneration and persist in an atypical but “primed” state and can be switched by systemic inflammation to provoke a classical pro-inflammatory profile with potentially deleterious consequences.http://www.sciencedirect.com/science/article/pii/S0969996107002677AxonNeurodegenerationMicrogliaLipopolysaccharide |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Karine Palin Colm Cunningham Penny Forse V. Hugh Perry Nick Platt |
spellingShingle |
Karine Palin Colm Cunningham Penny Forse V. Hugh Perry Nick Platt Systemic inflammation switches the inflammatory cytokine profile in CNS Wallerian degeneration Neurobiology of Disease Axon Neurodegeneration Microglia Lipopolysaccharide |
author_facet |
Karine Palin Colm Cunningham Penny Forse V. Hugh Perry Nick Platt |
author_sort |
Karine Palin |
title |
Systemic inflammation switches the inflammatory cytokine profile in CNS Wallerian degeneration |
title_short |
Systemic inflammation switches the inflammatory cytokine profile in CNS Wallerian degeneration |
title_full |
Systemic inflammation switches the inflammatory cytokine profile in CNS Wallerian degeneration |
title_fullStr |
Systemic inflammation switches the inflammatory cytokine profile in CNS Wallerian degeneration |
title_full_unstemmed |
Systemic inflammation switches the inflammatory cytokine profile in CNS Wallerian degeneration |
title_sort |
systemic inflammation switches the inflammatory cytokine profile in cns wallerian degeneration |
publisher |
Elsevier |
series |
Neurobiology of Disease |
issn |
1095-953X |
publishDate |
2008-04-01 |
description |
Axon loss in the CNS is characteristic of many neurodegenerative diseases but the mechanisms of axon degeneration are poorly understood. In particular, we know little of the inflammatory response triggered by CNS axon degeneration with comparison to that provoked by death of the neuronal cell body. We show that Wallerian degeneration of the mouse optic nerve induces transcription of TGF-β1 and TNF-α, but not pro-inflammatory cytokines IL-1β and IL-6 and microglial activation. This atypical inflammatory response resembles macrophages that have phagocytosed apoptotic cells and prion-infected CNS. Significantly, peripheral endotoxin challenge after injury switched this profile by inducing IL-1β, IL-6 transcripts, other inflammation-associated products and reducing neurofilament immunoreactivity. We propose that microglia are activated by Wallerian degeneration and persist in an atypical but “primed” state and can be switched by systemic inflammation to provoke a classical pro-inflammatory profile with potentially deleterious consequences. |
topic |
Axon Neurodegeneration Microglia Lipopolysaccharide |
url |
http://www.sciencedirect.com/science/article/pii/S0969996107002677 |
work_keys_str_mv |
AT karinepalin systemicinflammationswitchestheinflammatorycytokineprofileincnswalleriandegeneration AT colmcunningham systemicinflammationswitchestheinflammatorycytokineprofileincnswalleriandegeneration AT pennyforse systemicinflammationswitchestheinflammatorycytokineprofileincnswalleriandegeneration AT vhughperry systemicinflammationswitchestheinflammatorycytokineprofileincnswalleriandegeneration AT nickplatt systemicinflammationswitchestheinflammatorycytokineprofileincnswalleriandegeneration |
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