MICROGLIAL CLEARANCE FUNCTION IN HEALTH AND DISEASE

被引:249
作者
Napoli, I. [1 ]
Neumann, H. [1 ]
机构
[1] Univ Bonn & Hertie Fdn, Univ Bonn, Inst Reconstruct Neurobiol, LIFE & BRAIN Ctr, D-53127 Bonn, Germany
关键词
microglia; phagocytosis; microglial receptors; ITAM; CNS diseases; CEREBRAL ISCHEMIA/REPERFUSION INJURY; PROLIFERATING RESIDENT MICROGLIA; CLASS-I MHC; APOPTOTIC CELLS; CNS REMYELINATION; DROSOPHILA METAMORPHOSIS; PHAGOSOME MATURATION; ALZHEIMERS-DISEASE; MYELOID CELLS-2; IMMUNE-SYSTEM;
D O I
10.1016/j.neuroscience.2008.06.046
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Microglial cells are of hematopoietic origin, populate the CNS during early development and form the brain's innate immune cell type. Besides their well-known role in immune defense, microglia have an active and homeostatic function in the normal CNS based on high motility of their ramified processes and endocytic clearance of apoptotic vesicular material. During development microglia contribute to the reorganization of neuronal connections, however microglia have also pivotal roles during acute and chronic neurodegeneration. Microglia become attracted to site of injury by nucleotides released from damaged neurons. Scavenger receptors expressed on microglia bind to debris and microglial phagocytic receptors signal via immunoreceptor tyrosine-based activation motif (ITAM) -containing adaptor proteins to promote phagocytosis of extracellular material. Insufficient clearance by microglia appears to be prevalent in neurodegenerative diseases such as Alzheimer's disease. (C) 2009 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1030 / 1038
页数:9
相关论文
共 67 条
[1]   Essential role of the apoptotic cell engulfment genes draper and ced-6 in programmed axon pruning during Drosophila metamorphosis [J].
Awasaki, T ;
Tatsumi, R ;
Takahashi, K ;
Arai, K ;
Nakanishi, Y ;
Ueda, R ;
Ito, K .
NEURON, 2006, 50 (06) :855-867
[2]   Engulfing action of glial cells is required for programmed axon pruning during Drosophila metamorphosis [J].
Awasaki, T ;
Ito, K .
CURRENT BIOLOGY, 2004, 14 (08) :668-677
[3]   Neuronal 'On' and 'Off' signals control microglia [J].
Biber, Knut ;
Neumann, Harald ;
Inoue, Kazuhide ;
Boddeke, Hendrikus W. G. M. .
TRENDS IN NEUROSCIENCES, 2007, 30 (11) :596-602
[4]   Axon branch removal at developing synapses by axosome shedding [J].
Bishop, DL ;
Misgeld, T ;
Walsh, MK ;
Gan, WB ;
Lichtman, JW .
NEURON, 2004, 44 (04) :651-661
[5]   Regulation of phagosome maturation by signals from Toll-like receptors [J].
Blander, JM ;
Medzhitov, R .
SCIENCE, 2004, 304 (5673) :1014-1018
[6]   Dynamics of the microglial/amyloid interaction indicate a role in plaque maintenance [J].
Bolmont, Tristan ;
Haiss, Florent ;
Eicke, Daniel ;
Radde, Rebecca ;
Mathis, Chester A. ;
Klunk, William E. ;
Kohsaka, Shinichi ;
Jucker, Mathias ;
Calhoun, Michael E. .
JOURNAL OF NEUROSCIENCE, 2008, 28 (16) :4283-4292
[7]   Immune cells may fend off Alzheimer disease [J].
Britschgi, Markus ;
Wyss-Coray, Tony .
NATURE MEDICINE, 2007, 13 (04) :408-409
[8]   Axon pruning: An active role for glial cells [J].
Broadie, K .
CURRENT BIOLOGY, 2004, 14 (08) :R302-R304
[9]   Control of microglial neurotoxicity by the fractalkine receptor [J].
Cardona, Astrid E. ;
Pioro, Erik P. ;
Sasse, Margaret E. ;
Kostenko, Volodymyr ;
Cardona, Sandra M. ;
Dijkstra, Ineke M. ;
Huang, DeRen ;
Kidd, Grahame ;
Dombrowski, Stephen ;
Dutta, RanJan ;
Lee, Jar-Chi ;
Cook, Donald N. ;
Jung, Steffen ;
Lira, Sergio A. ;
Littman, Dan R. ;
Ransohoff, Richard M. .
NATURE NEUROSCIENCE, 2006, 9 (07) :917-924
[10]   Trems in the immune system and beyond [J].
Colonna, M .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (06) :445-453