Cell type-specific expression of neuropilins in an MCA-occlusion model in mice suggests a potential role in post-ischemic brain remodeling

被引:96
作者
Beck, H
Acker, T
Püschel, AW
Fujisawa, H
Carmeliet, P
Plate, KH
机构
[1] Goethe Univ Frankfurt, Inst Neurol, Edinger Inst, D-60528 Frankfurt, Germany
[2] Max Planck Inst Brain Res, Dept Neurochem, D-60496 Frankfurt, Germany
[3] Nagoya Univ, Grad Sch Sci, Div Biol Sci, Grp Dev Neurobiol,Chikusa Ku, Nagoya, Aichi 466, Japan
[4] Katholieke Univ Leuven VIB, Ctr Transgene Technol & Gene Therapy, B-3001 Louvain, Belgium
关键词
angiogenesis; class III semaphorins; neuropilin; placenta growth factor; stroke; vascular endothelial growth factor;
D O I
10.1093/jnen/61.4.339
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neuropilin-1 and -2 (NP-1/NP-2) are transmembrane receptors that play a role in axonal guidance by binding of class III semaphorins, and in angiogenesis by binding of the vascular endothelial growth factor isoform VEGF, and placenta growth factor (PLGF). We investigated the expression pattern of NP-1/NP-2. their co-receptors, vascular endothelial growth factor receptor-1 and -2 (VEGFR-1, VEGFR-2), and their ligands, class III semaphorins, VEGF and PLGF, following experimental cerebral ischemia in mice. By means of in situ hybridization and immunohistochemistry we observed loss of expression of class III semaphorins in neurons in the infarct/peri-infarct area. In contrast, we observed high expression of NP-1 in vessels. neurons, and astrocytes surrounding the infarct. VEGF and PLGF were upregulated in different cell types following stroke. Our results suggest a shift in the balance between semaphorins and VEGF/PLGF, which compete for NP-binding. Possibly, the loss of semaphorins facilitates binding of the competing ligands (VEGF/PLGF), thus inducing angiogenesis. In addition. the observed expression patterns further suggest a neurotrophic/neuroprotective role of VEGF/PLGF.
引用
收藏
页码:339 / 350
页数:12
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