Reactive astrocytes of the quinolinc acid-lesioned rat striatum express GFRα1 as well as GDNF in vivo

被引:70
作者
Bresjanac, M [1 ]
Antauer, G [1 ]
机构
[1] Univ Ljubljana, Sch Med, Inst Pathophysiol, Lab Neuronal Plast & Regenerat, Ljubljana 1104, Slovenia
关键词
GDNF; GFR alpha 1; glia; excitotoxicity; immunofluorescence; confocal microscopy; immunohistochemistry;
D O I
10.1006/exnr.2000.7416
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mechanical injury of the rodent striatum has recently been shown to cause a local increase in expression of mRNAs for glial cell line-derived neurotrophic factor (GDNF) and brain-derived neurotrophic factor in the inflammatory cells, i.e., macrophages and activated microglia, respectively (3). An earlier study demonstrated an increase in GDNF mRNA levels in the adult rat striatum after administration of subseizure doses of N-methyl-D,L-aspartate and kainic acid (20) and identified astrocytes as the likely source of GDNF mRNA in the injected striatum. Our own recent work suggests that quinolinic acid (QA) induces moderate immunoreactivity to GDNF in a population of cells resembling reactive astrocytes within 1 week following intrastriatal injection (9). Therefore, the present follow-up experiment was performed with the aims: (I) to look at GDNF expression in the QA-injected striatum at 28 days, (II) to look for possible immunohistochemical expression of GFR alpha 1 in the QA-injected striatum at the same observation time, and (III) to use confocal microscopy of double-immunofluorescence labeling of glial-cell-specific markers to identify the cell types expressing GDNF and GFR alpha 1 in the striatum at 28 days following a QA injection. Our data indicate that GDNF immunoreactivity is high in the BA-injected striatum at 28 days and that the vast majority of cells displaying high labeling for GDNF also express glial fibrillary acidic protein and have a phenotype of reactive astrocytes. Interestingly, the same cells that express GDNF also display strong cytoplasmic immunolabeling to GFR alpha 1. (C) 2000 Academic Press.
引用
收藏
页码:53 / 59
页数:7
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