Are chemokines the third major system in the brain?

被引:110
作者
Adler, MW
Rogers, TJ
机构
[1] Temple Univ, Sch Med, Ctr Subst Abuse Res, Philadelphia, PA 19140 USA
[2] Temple Univ, Sch Med, Fels Inst Canc Res & Mol Biol, Philadelphia, PA 19140 USA
[3] Temple Univ, Sch Med, Dept Pharmacol, Philadelphia, PA 19140 USA
关键词
opioids; heterologous desensitization; neuromodulators; interneuronal communication;
D O I
10.1189/jlb.0405222
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chemokines are a family of small proteins involved in cellular migration and intercellular communication. Although the chemokines and their receptors are located throughout the brain, they are not distributed uniformly. Among the chemokines and their receptors that are arrayed disproportionately in glia and neurons are monocyte chemotactic protein-1/CC chemokine ligand 2 (CCL2), stromal cell-derived factor-1/CXC chemokine ligand 12 (CXCL12), fractalkine/CX3C chemokine ligand 1, interferon-gamma-inducible-protein-10/CXCL10, macrophage inflammatory protein-1 alpha/CCL3, and regulated on activation, normal T cell expressed and secreted/CCL5. In the brain, they are found in the hypothalamus, nucleus accumbens, limbic system, hippocampus, thalamus, cortex, and cerebellum. The uneven distribution suggests that there may be functional roles for the chemokine "system," comprised of chemokine ligands and their receptors. In addition to anatomical, immunohistochemical, and in vitro studies establishing the expression of the chemokine ligands and receptors, there is an increasing body of research that suggests that the chemokine system plays a crucial role in brain development and function. Our data indicate that the chemokine system can alter the actions of neuronally active pharmacological agents including the opioids and cannabinoids. Combined with evidence that the chemokine system in the brain interacts with neurotransmitter systems, we propose the following hypothesis: The endogenous chemokine system in the brain acts in concert with the neurotransmitter and neuropeptide systems to govern brain function. The chemokine system can thus be thought of as the third major transmitter system in the brain.
引用
收藏
页码:1204 / 1209
页数:6
相关论文
共 39 条
[1]   Chemoattractant receptor cross-desensitization [J].
Ali, H ;
Richardson, RM ;
Haribabu, B ;
Snyderman, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (10) :6027-6030
[2]   Chemokines and glial cells: A complex network in the central nervous system [J].
Ambrosini, E ;
Aloisi, F .
NEUROCHEMICAL RESEARCH, 2004, 29 (05) :1017-1038
[3]  
Bagri A, 2002, DEVELOPMENT, V129, P4249
[4]   Characterization of chemokines and their receptors in the central nervous system: physiopathological implications [J].
Bajetto, A ;
Bonavia, R ;
Barbero, S ;
Schettini, G .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (06) :1311-1329
[5]   Chemokines and their receptors in the central nervous system [J].
Bajetto, A ;
Bonavia, R ;
Barbero, S ;
Florio, T ;
Schettini, G .
FRONTIERS IN NEUROENDOCRINOLOGY, 2001, 22 (03) :147-184
[6]   Neuroanatomical distribution of CXCR4 in adult rat brain and its localization in cholinergic and dopaminergic neurons [J].
Banisadr, G ;
Fontanges, P ;
Haour, F ;
Kitabgi, P ;
Rostène, W ;
Parsadaniantz, SM .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2002, 16 (09) :1661-1671
[7]   Distribution, cellular localization and functional role of CCR2 chemokine receptors in adult rat brain [J].
Banisadr, G ;
Quéraud-Lesaux, F ;
Boutterin, MC ;
Pélaprat, D ;
Zalc, B ;
Rostène, W ;
Haour, F ;
Parsadaniantz, SM .
JOURNAL OF NEUROCHEMISTRY, 2002, 81 (02) :257-269
[8]   Role of genetic background in P selectin-dependent immune surveillance of the central nervous system [J].
Carrithers, MD ;
Visintin, I ;
Viret, C ;
Janeway, CA .
JOURNAL OF NEUROIMMUNOLOGY, 2002, 129 (1-2) :51-57
[9]   Heterodimerization and cross-desensitization between the μ-opioid receptor and the chemokine CCR5 receptor [J].
Chen, CG ;
Li, J ;
Bot, G ;
Szabo, I ;
Rogers, TJ ;
Liu-Chen, LY .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2004, 483 (2-3) :175-186
[10]   Chemokine receptors and neural function [J].
Cho, C ;
Miller, RJ .
JOURNAL OF NEUROVIROLOGY, 2002, 8 (06) :573-584