Production of monocyte chemoattractant protein-1 in amyotrophic lateral sclerosis

被引:96
作者
Baron, P
Bussini, S
Cardin, V
Corbo, M
Conti, G
Galimberti, D
Scarpini, E
Bresolin, N
Wharton, SB
Shaw, PJ
Silani, V
机构
[1] Univ Milan, Sch Med, Dept Neurol Sci,Dino Ferrari Ctr, IRCCS,Osped Maggiore Policlin, I-20122 Milan, Italy
[2] Univ Milan, Sch Med, IRCCS,Ist Auxol Italiano, Dept Neurol, I-20122 Milan, Italy
[3] Univ Milan, Sch Med, IRCCS,Ist Auxol Italiano, Neurosci Lab, I-20122 Milan, Italy
[4] Univ Sheffield, Acad Unit Pathol, Sheffield, S Yorkshire, England
[5] Univ Sheffield, Acad Unit Neurol, Sheffield, S Yorkshire, England
基金
英国惠康基金;
关键词
amyotrophic lateral sclerosis; astrocytes; chemokines; inflammation; microglia; neurons; spinal cord;
D O I
10.1002/mus.20376
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The presence of activated microglia in the spinal cord of amyotrophic lateral sclerosis (ALS) patients is usually accompanied by inflammatory biochemical changes, but these are largely unexplored. Monocyte chemoattractant protein-1 (MCP-1) is critical for recruitment of inflammatory cells of monocytic lineage after inflammation or injury to the central nervous system. MCP-1 concentrations were measured by an enzyme-linked immunosorbent assay in the cerebrospinal fluid (CSF) and the serum of 27 patients with ALS and 30 patients with noninflammatory neurological diseases. In ALS, circulating MCP-1 levels were significantly increased in the serum and particularly in the CSF. Immunoreactivity for MCP-1 in ALS spinal cord was detected mostly in astrocytes but also in microglia, neurons, and within the vasculature of the cord. Our findings suggest a role for MCP-1 as an important molecular mediator of the injury response in ALS.
引用
收藏
页码:541 / 544
页数:4
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