Document Detail


Neural injury following stroke: are Toll-like receptors the link between the immune system and the CNS?
MedLine Citation:
PMID:  20649586     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The CNS can exhibit features of inflammation in response to injury, infection or disease, whereby resident cells generate inflammatory mediators, including cytokines, prostaglandins, free radicals and complement, chemokines and adhesion molecules that recruit immune cells, and activate glia and microglia. Cerebral ischaemia triggers acute inflammation, which exacerbates primary brain damage. The regulation of inflammation after stroke is multifaceted and comprises vascular effects, distinct cellular responses, apoptosis and chemotaxis. There are many cell types that are affected including neurons, astrocytes, microglia and endothelial cells, all responding to the resultant neuroinflammation in different ways. Over the past 20 years, researchers examining brain tissue at various time intervals after stroke observed the presence of inflammatory cells, neutrophils and monocytes at the site of injury, as well as the activation of endogenous glia and microglia. This review examines the involvement of these cells in the progression of neural injury and proposes that the Toll-like receptors (TLRs) are likely to be an integral component in the communication between the CNS and the periphery. This receptor system is the archetypal pathogen sensing receptor system and its presence and signalling in the brain following neural injury suggests a more diverse role. We propose that the TLR system presents excellent pharmacological targets for the design of a new generation of therapeutic agents to modulate the inflammation that accompanies neural injury.
Authors:
Catherine E Downes; Peter J Crack
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review    
Journal Detail:
Title:  British journal of pharmacology     Volume:  160     ISSN:  1476-5381     ISO Abbreviation:  Br. J. Pharmacol.     Publication Date:  2010 Aug 
Date Detail:
Created Date:  2010-07-23     Completed Date:  2010-11-08     Revised Date:  2011-08-03    
Medline Journal Info:
Nlm Unique ID:  7502536     Medline TA:  Br J Pharmacol     Country:  England    
Other Details:
Languages:  eng     Pagination:  1872-88     Citation Subset:  IM    
Affiliation:
Department of Pharmacology, The University of Melbourne, Parkville, Victoria, Australia.
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MeSH Terms
Descriptor/Qualifier:
Animals
Anti-Inflammatory Agents / pharmacology
Humans
Immunity, Innate
Inflammation / immunology*,  pathology,  prevention & control
Inflammation Mediators / metabolism
Neurons / drug effects,  immunology*,  pathology
Neuroprotective Agents / pharmacology
Signal Transduction* / drug effects
Stroke / drug therapy,  immunology*,  pathology
Toll-Like Receptors / drug effects,  metabolism*
Chemical
Reg. No./Substance:
0/Anti-Inflammatory Agents; 0/Inflammation Mediators; 0/Neuroprotective Agents; 0/Toll-Like Receptors
Comments/Corrections

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