Microglia: Mechanisms of activation and involvement in the pathogenesis of neuropsychiatric diseases

被引:4
作者
Gebicke-Haerter, PJ
Lieb, K
Illes, P
Berger, M
机构
[1] Univ Freiburg, Psychiat Klin, D-79104 Freiburg, Germany
[2] Univ Leipzig, Inst Pharmakol, D-7010 Leipzig, Germany
来源
NERVENARZT | 1998年 / 69卷 / 09期
关键词
adenosine; AIDS-dementia; Alzheimer's dementia; EAE; K+-channels; voltage-dependent; microglia; multiple sclerosis; proliferation; purinoceptors; regeneration; cytotoxicity;
D O I
10.1007/s001150050339
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Microglia are the resident macrophages of the brain. They are the central cellular element to initiate defense mechanisms against destructive environmental influences and to facilitate regenerative processes. No other cell type of the brain is endowed with a comparably comprehensive, immunocompetent machinery like microglia. It encompasses cell proliferation, migration and differentiation into full-blown macrophages able to present antigen and to phagocytose cell debris. Relatively little is known about these stages of microglia activation on the cellular and molecular level, although microglia have been described as a separate cell type of the brain as early as in the 30ies of this century by P. del Rio Hortega. This review summarizes the data that have accumulated until now in this respect and tries to embed them into a clinical framework. Special focus has been given to the role of this cell type in the development and progression of Multiple Sclerosis, HIV-associated dementia and Alzheimer's disease.
引用
收藏
页码:752 / 762
页数:21
相关论文
共 128 条
[1]   THE ROLE OF THE ACUTE-PHASE PROTEIN ALPHA-1-ANTICHYMOTRYPSIN IN BRAIN-DYSFUNCTION AND INJURY [J].
ABRAHAM, CR .
RESEARCH IN IMMUNOLOGY, 1992, 143 (06) :631-636
[2]  
Alzheimer A., 1907, ALLG Z PSYCHIAT, V64, P146, DOI DOI 10.1002/CA.980080612
[3]   INTRACEREBRAL INJECTION OF PROINFLAMMATORY CYTOKINES OR LEUKOCYTE CHEMOTAXINS INDUCES MINIMAL MYELOMONOCYTIC CELL RECRUITMENT TO THE PARENCHYMA OF THE CENTRAL-NERVOUS-SYSTEM [J].
ANDERSSON, PB ;
PERRY, VH ;
GORDON, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (01) :255-259
[4]   EXPRESSION OF INTERLEUKIN-3 AND TUMOR NECROSIS FACTOR-BETA MESSENGER-RNAS IN CULTURED MICROGLIA [J].
APPEL, K ;
HONEGGER, P ;
GEBICKEHAERTER, PJ .
JOURNAL OF NEUROIMMUNOLOGY, 1995, 60 (1-2) :83-91
[5]  
APPEL K, 1995, J NEUROSCI, V15, P5800
[6]   BETA-AMYLOID STIMULATES GLIAL-CELLS INVITRO TO PRODUCE GROWTH-FACTORS THAT ACCUMULATE IN SENILE PLAQUES IN ALZHEIMERS-DISEASE [J].
ARAUJO, DM ;
COTMAN, CW .
BRAIN RESEARCH, 1992, 569 (01) :141-145
[7]   HIV blocked by chemokine antagonist [J].
ArenzanaSeisdedos, F ;
Virelizier, JL ;
Rousset, D ;
ClarkLewis, I ;
Loetscher, P ;
Moser, B ;
Baggiolini, M .
NATURE, 1996, 383 (6599) :400-400
[8]   Interferon beta in multiple sclerosis [J].
Arnason, BGW .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1996, 81 (01) :1-11
[9]   Activation of the inducible form of nitric oxide synthase in the brains of patients with multiple sclerosis [J].
Bagasra, O ;
Michaels, FH ;
Zheng, YM ;
Bobroski, LE ;
Spitsin, SV ;
Fu, ZF ;
Tawadros, R ;
Koprowski, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (26) :12041-12045
[10]   SURVEILLANCE, INTERVENTION AND CYTOTOXICITY - IS THERE A PROTECTIVE ROLE OF MICROGLIA [J].
BANATI, RB ;
GRAEBER, MB .
DEVELOPMENTAL NEUROSCIENCE, 1994, 16 (3-4) :114-127