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Erschienen in: NeuroMolecular Medicine 2/2010

01.06.2010 | Original Paper

The Role of the Complement System and the Activation Fragment C5a in the Central Nervous System

verfasst von: Trent M. Woodruff, Rahasson R. Ager, Andrea J. Tenner, Peter G. Noakes, Stephen M. Taylor

Erschienen in: NeuroMolecular Medicine | Ausgabe 2/2010

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Abstract

The complement system is a pivotal component of the innate immune system which protects the host from infection and injury. Complement proteins can be induced in all cell types within the central nervous system (CNS), where the pathway seems to play similar roles in host defense. Complement activation produces the C5 cleavage fragment C5a, a potent inflammatory mediator, which recruits and activates immune cells. The primary cellular receptor for C5a, the C5a receptor (CD88), has been reported to be on all CNS cells, including neurons and glia, suggesting a functional role for C5a in the CNS. A second receptor for C5a, the C5a-like receptor 2 (C5L2), is also expressed on these cells; however, little is currently known about its potential role in the CNS. The potent immune and inflammatory actions of complement activation are necessary for host defense. However, if over-activated, or left unchecked it promotes tissue injury and contributes to brain disease pathology. Thus, complement activation, and subsequent C5a generation, is thought to play a significant role in the progression of CNS disease. Paradoxically, complement may also exert a neuroprotective role in these diseases by aiding in the elimination of aggregated and toxic proteins and debris which are a principal hallmark of many of these diseases. This review will discuss the expression and known roles for complement in the CNS, with a particular focus on the pro-inflammatory end-product, C5a. The possible overarching role for C5a in diseases of the CNS is reviewed, and the therapeutic potential of blocking C5a/CD88 interaction is evaluated.
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Zurück zum Zitat Osaka, H., Mukherjee, P., Aisen, P. S., & Pasinetti, G. M. (1999b). Complement-derived anaphylatoxin C5a protects against glutamate-mediated neurotoxicity. Journal of Cellular Biochemistry, 73, 303–311.PubMed Osaka, H., Mukherjee, P., Aisen, P. S., & Pasinetti, G. M. (1999b). Complement-derived anaphylatoxin C5a protects against glutamate-mediated neurotoxicity. Journal of Cellular Biochemistry, 73, 303–311.PubMed
Zurück zum Zitat Otto, M., Hawlisch, H., Monk, P. N., Muller, M., Klos, A., Karp, C. L., et al. (2004). C5a mutants are potent antagonists of the C5a receptor (CD88) and of C5L2: Position 69 is the locus that determines agonism or antagonism. Journal of Biological Chemistry, 279, 142–151.PubMed Otto, M., Hawlisch, H., Monk, P. N., Muller, M., Klos, A., Karp, C. L., et al. (2004). C5a mutants are potent antagonists of the C5a receptor (CD88) and of C5L2: Position 69 is the locus that determines agonism or antagonism. Journal of Biological Chemistry, 279, 142–151.PubMed
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Zurück zum Zitat Podack, E. R., Tschoop, J., & Muller-Eberhard, H. J. (1982). Molecular organization of C9 within the membrane attack complex of complement. Induction of circular C9 polymerization by the C5b–8 assembly. Journal of Experimental Medicine, 156, 268–282.PubMed Podack, E. R., Tschoop, J., & Muller-Eberhard, H. J. (1982). Molecular organization of C9 within the membrane attack complex of complement. Induction of circular C9 polymerization by the C5b–8 assembly. Journal of Experimental Medicine, 156, 268–282.PubMed
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Metadaten
Titel
The Role of the Complement System and the Activation Fragment C5a in the Central Nervous System
verfasst von
Trent M. Woodruff
Rahasson R. Ager
Andrea J. Tenner
Peter G. Noakes
Stephen M. Taylor
Publikationsdatum
01.06.2010
Verlag
Humana Press Inc
Erschienen in
NeuroMolecular Medicine / Ausgabe 2/2010
Print ISSN: 1535-1084
Elektronische ISSN: 1559-1174
DOI
https://doi.org/10.1007/s12017-009-8085-y

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