Article (Scientific journals)
Distinct modulation of microglial amyloid β phagocytosis and migration by neuropeptides (i).
Fleisher-Berkovich, Sigal; Filipovich-Rimon, Talia; Ben-Shmuel, Sarit et al.
2010In Journal of Neuroinflammation, 7 (1), p. 61
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Keywords :
Amyloid beta-Peptides; Receptors, Bradykinin; Receptors, Endothelin; Receptors, Somatostatin; Nitric Oxide Synthase Type II; Cyclooxygenase 2; Amyloid beta-Peptides/metabolism; Analysis of Variance; Animals; Blotting, Western; Cell Line; Cell Movement/physiology; Cells, Cultured; Cyclooxygenase 2/genetics; Cyclooxygenase 2/metabolism; Immunohistochemistry; Mice; Microglia/metabolism; Nitric Oxide Synthase Type II/genetics; Nitric Oxide Synthase Type II/metabolism; Phagocytosis/physiology; Receptors, Bradykinin/metabolism; Receptors, Endothelin/metabolism; Receptors, Somatostatin/metabolism; Reverse Transcriptase Polymerase Chain Reaction; Neuroscience (all); Immunology; Neurology; Cellular and Molecular Neuroscience; General Neuroscience
Abstract :
[en] Microglial activation plays an integral role in the development and course of neurodegeneration. Although neuropeptides such as bradykinin (BK), somatostatin (SST), and endothelin (ET) are known to be important mediators of inflammation in the periphery, evidence of a similar function in brain is scarce. Using immunocytochemistry, we demonstrate the expression of receptors for BK (B1, B2 subtypes), ET (ETA, ETB subtypes) and SST (SST 2, 3, 4 subtypes) in primary microglia and microglial cell lines. Exposure of BV2 and N9, as well as primary microglial cells to BK or SST increased Aβ uptake in a concentration-dependent manner, whereas endothelin decreased Aβ uptake. This was caused by increased phagocytosis of Aβ since the rate of intracellular Aβ degradation remained unaffected. All neuropeptides increased chemotactic activity of microglia. In addition, BK reduced Aβ-induced expression of proinflammatory genes including iNOS and COX-2. ET decreased the Aβ-induced expression of monocyte chemoattractant protein 1 and interleukin-6. These results suggest that neuropeptides play an important role in chemotaxis and Aβ clearance and modulate the brain's response to neuroinflammatory processes.
Disciplines :
Neurology
Author, co-author :
Fleisher-Berkovich, Sigal;  Division of Clinical Neurosciences, Dept. of Neurology, University of Bonn Medical Center, Bonn, Germany
Filipovich-Rimon, Talia;  Faculty of Health Sciences, Dept. of Clinical Pharmacology, Ben-Gurion University of the Negev, Beer-Sheva, Israel
Ben-Shmuel, Sarit;  Faculty of Health Sciences, Dept. of Clinical Pharmacology, Ben-Gurion University of the Negev, Beer-Sheva, Israel
Hülsmann, Claudia;  Division of Clinical Neurosciences, Dept. of Neurology, University of Bonn Medical Center, Bonn, Germany
Kummer, Markus P;  Division of Clinical Neurosciences, Dept. of Neurology, University of Bonn Medical Center, Bonn, Germany
HENEKA, Michael  ;  Division of Clinical Neurosciences, Dept. of Neurology, University of Bonn Medical Center, Bonn, Germany
External co-authors :
yes
Language :
English
Title :
Distinct modulation of microglial amyloid β phagocytosis and migration by neuropeptides (i).
Publication date :
11 October 2010
Journal title :
Journal of Neuroinflammation
eISSN :
1742-2094
Publisher :
Springer Science and Business Media LLC, England
Volume :
7
Issue :
1
Pages :
61
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBilu :
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