Glia: guardians, gluttons, or guides for the maintenance of neuronal connectivity?

被引:21
作者
Jebelli, Joseph [1 ]
Su, Wei [1 ]
Hopkins, Stephanie [1 ]
Pocock, Jennifer [2 ]
Garden, Gwenn A. [1 ]
机构
[1] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
[2] UCL, Inst Neurol, Dept Neuroinflammat, London, England
来源
NEUROIMMUNOMODULATION IN HEALTH AND DISEASE | 2015年 / 1351卷
关键词
synapse; glia; neurodegeneration; OLIGODENDROCYTE PRECURSOR CELLS; ALZHEIMERS-DISEASE; NMDA RECEPTOR; WHITE-MATTER; TRANSMITTER RELEASE; SYNAPTIC INPUT; IN-VIVO; MICROGLIA; ASTROCYTES; SYNAPSES;
D O I
10.1111/nyas.12711
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An emerging aspect of neuronal-glial interactions is the connection glial cells have to synapses. Mounting research nowsuggests a farmore intimate relationship than previously recognized. Moreover, the current evidence implicating synapse loss in neurodegenerative disease etiology is overwhelming, but the role of glia in the process of synaptic degeneration has only recently been considered in earnest. Each main class of glial cell, including astrocytes, oligodendrocytes, and microglia, performs crucial and multifaceted roles in the maintenance of synaptic function and excitability. As such, aging and/or neuronal stress from disease-related misfolded proteins may involve disruption of multiple non-cell-autonomous synaptic support systems that are mediated by neighboring glia. In addition, glial cell activation induced by injury, ischemia, or neurodegeneration is thought to greatly alter the behavior of glial cells toward neuronal synapses, suggesting that neuroinflammation potentially contributes to synapse loss primarily mediated by altered glial functions. This review discusses recent evidence highlighting novel roles for glial cells at neuronal synapses and in the maintenance of neuronal connectivity, focusing primarily on their implications for neurodegenerative disease research.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 94 条
[1]   Glia: The many ways to modulate synaptic plasticity [J].
Achour, S. Ben ;
Pascual, O. .
NEUROCHEMISTRY INTERNATIONAL, 2010, 57 (04) :440-445
[2]   Astrocyte glypicans 4 and 6 promote formation of excitatory synapses via GluA1 AMPA receptors [J].
Allen, Nicola J. ;
Bennett, Mariko L. ;
Foo, Lynette C. ;
Wang, Gordon X. ;
Chakraborty, Chandrani ;
Smith, Stephen J. ;
Barres, Ben A. .
NATURE, 2012, 486 (7403) :410-+
[3]   The role of neuronal activity and transmitter release on synapse formation [J].
Andreae, Laura C. ;
Burrone, Juan .
CURRENT OPINION IN NEUROBIOLOGY, 2014, 27 :47-52
[4]  
Araque A, 1998, J NEUROSCI, V18, P6822
[5]   Accelerated microglial pathology is associated with Aβ plaques in mouse models of Alzheimer's disease [J].
Baron, Rona ;
Babcock, Alicia A. ;
Nemirovsky, Anna ;
Finsen, Bente ;
Monsonego, Alon .
AGING CELL, 2014, 13 (04) :584-595
[6]   Glutamatergic synapses on oligodendrocyte precursor cells in the hippocampus [J].
Bergles, DE ;
Roberts, JDB ;
Somogyi, P ;
Jahr, CE .
NATURE, 2000, 405 (6783) :187-191
[7]   Microglial control of neuronal death and synaptic properties [J].
Bessis, Alain ;
Bechade, Catherine ;
Bernard, Delphine ;
Roumier, Anne .
GLIA, 2007, 55 (03) :233-238
[8]   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
[9]   Microglia-mediated neurotoxicity: uncovering the molecular mechanisms [J].
Block, Michelle L. ;
Zecca, Luigi ;
Hong, Jau-Shyong .
NATURE REVIEWS NEUROSCIENCE, 2007, 8 (01) :57-69
[10]   Expression of mutant huntingtin in mouse brain astrocytes causes age-dependent neurological symptoms [J].
Bradford, Jennifer ;
Shin, Ji-Yeon ;
Roberts, Meredith ;
Wang, Chuan-En ;
Li, Xiao-Jiang ;
Li, Shihua .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (52) :22480-22485