IL-1-regulated responses in astrocytes: Relevance to injury and recovery

被引:153
作者
John, GR
Lee, SC
Song, XY
Rivieccio, M
Brosnan, CF
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10461 USA
[2] CUNY Mt Sinai Sch Med, Corinne Goldsmith Dickinson Ctr Multiple Sclerosi, Dept Neurol, New York, NY 10029 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
关键词
astrocytes; IL-1-regulated responses; injury; recovery;
D O I
10.1002/glia.20109
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the central nervous system (CNS), the cellular processes of astrocytes make intimate contact with essentially all areas of the brain. They have also been shown to be functionally coupled to neurons, oligodendrocytes. and other astrocytes via both contact-dependent and non-contact-dependent pathways. These observations have led to the suggestion that a major function of astrocytes in the CNS is to maintain the homeostatic environment, thus promoting the proper functioning of the neuronal network. Inflammation in the CNS disrupts this process either transiently or permanently and, as such, is thought to be tightly regulated by both astrocytes and microglia. The remarkable role that single cytokines, such as TNF and IL-1, may play in this process: has now been well accepted, but the extent of the reprogramming of the transcriptional machinery initiated by these factors remains to be fully appreciated. With the advent of microarray technology, a more comprehensive analysis of this process is now available. In this report we review data obtained with this technology to provide an overview of the extent of changes induced in astrocytes by the cytokine IL-1. (C) 2004 Wiley-Liss, Inc
引用
收藏
页码:161 / 176
页数:16
相关论文
共 146 条
[31]   Identification of a major co-receptor for primary isolates of HIV-1 [J].
Deng, HK ;
Liu, R ;
Ellmeier, W ;
Choe, S ;
Unutmaz, D ;
Burkhart, M ;
DiMarzio, P ;
Marmon, S ;
Sutton, RE ;
Hill, CM ;
Davis, CB ;
Peiper, SC ;
Schall, TJ ;
Littman, DR ;
Landau, NR .
NATURE, 1996, 381 (6584) :661-666
[32]   Immune function of astrocytes [J].
Dong, YS ;
Benveniste, EN .
GLIA, 2001, 36 (02) :180-190
[33]   Lack of tumor necrosis factor-related apoptosis-inducing ligand but presence of its receptors in the human brain -: art. no. RC209 [J].
Dörr, J ;
Bechmann, I ;
Waiczies, S ;
Aktas, O ;
Walczak, H ;
Krammer, PH ;
Nitsch, R ;
Zipp, F .
JOURNAL OF NEUROSCIENCE, 2002, 22 (04)
[34]   HIV-1 entry into CD4(+) cells is mediated by the chemokine receptor CC-CKR-5 [J].
Dragic, T ;
Litwin, V ;
Allaway, GP ;
Martin, SR ;
Huang, YX ;
Nagashima, KA ;
Cayanan, C ;
Maddon, PJ ;
Koup, RA ;
Moore, JP ;
Paxton, WA .
NATURE, 1996, 381 (6584) :667-673
[35]   Interleukin-11: Review of molecular, cell biology, and clinical use [J].
Du, XX ;
Williams, DA .
BLOOD, 1997, 89 (11) :3897-3908
[36]   P2X7 receptor-mediated release of excitatory amino acids from astrocytes [J].
Duan, SM ;
Anderson, CM ;
Keung, EC ;
Chen, YM ;
Chen, YR ;
Swanson, RA .
JOURNAL OF NEUROSCIENCE, 2003, 23 (04) :1320-1328
[37]   Cell surface heparan sulfate proteoglycan syndecan-2 induces the maturation of dendritic spines in rat hippocampal neurons [J].
Ethell, IM ;
Yamaguchi, Y .
JOURNAL OF CELL BIOLOGY, 1999, 144 (03) :575-586
[38]   Reactive astrocytes protect tissue and preserve function after spinal cord injury [J].
Faulkner, JR ;
Herrmann, JE ;
Woo, MJ ;
Tansey, KE ;
Doan, NB ;
Sofroniew, MV .
JOURNAL OF NEUROSCIENCE, 2004, 24 (09) :2143-2155
[39]   The glial scar and central nervous system repair [J].
Fawcett, JW ;
Asher, RA .
BRAIN RESEARCH BULLETIN, 1999, 49 (06) :377-391
[40]   NOREPINEPHRINE SUPPRESSES INDUCIBLE NITRIC-OXIDE SYNTHASE ACTIVITY IN RAT ASTROGLIAL CULTURES [J].
FEINSTEIN, DL ;
GALEA, E ;
REIS, DJ .
JOURNAL OF NEUROCHEMISTRY, 1993, 60 (05) :1945-1948