Sondell M, Lundborg G, Kanje M
Department of Animal Physiology, Lund University, Helgonav. 3 B, S-223 62, Lund, Sweden.
Brain Res. 1999 Nov 6;846(2):219-28. doi: 10.1016/s0006-8993(99)02056-9.
The aim of this study was to investigate the effects of vascular endothelial growth factor (VEGF) on regeneration of the rat sciatic nerve in vivo. To that end we used 10-mm long cell-free nerve grafts to bridge a gap in the sciatic nerve. The grafts were pretreated with either VEGF (50, 100 or 250 ng/ml), nerve growth factor (NGF, 100 ng/ml) or laminin (100 ng/ml) before implantation. Outgrowth of axons, Schwann cells, blood vessels and macrophages were studied 10 days post-implantation by the use of immunocytochemistry and histochemistry. Grafts pretreated with VEGF stimulated the outgrowth of Schwann cells and blood vessels but not axons. In such grafts, the Schwann cells also exhibited a dramatic change in morphology and became filled with large lipid-containing vacuoles. These cells also showed an intense immunoreactivity for the VEGF receptor flk-1. Neither pretreatment with laminin nor NGF affected the outgrowth of Schwann cells. However, NGF treatment increased the number of axons in the graft but was not able to counteract injury-induced downregulation of substance P in the dorsal root ganglia. The results show that local application of VEGF promotes at least two events, invasion of Schwann cells and neovascularization, which are important during nerve regeneration. The findings suggest that the effects of the pretreatment by the growth factors is local and limited to the graft, whereas central events like neuropeptide synthesis is not affected.
本研究的目的是在体内研究血管内皮生长因子(VEGF)对大鼠坐骨神经再生的影响。为此,我们使用10毫米长的无细胞神经移植物来桥接坐骨神经的间隙。在植入前,移植物分别用VEGF(50、100或250 ng/ml)、神经生长因子(NGF,100 ng/ml)或层粘连蛋白(100 ng/ml)进行预处理。植入后10天,通过免疫细胞化学和组织化学研究轴突、施万细胞、血管和巨噬细胞的生长情况。用VEGF预处理的移植物刺激了施万细胞和血管的生长,但未刺激轴突生长。在这类移植物中,施万细胞的形态也发生了显著变化,充满了含大量脂质的空泡。这些细胞对VEGF受体flk-1也表现出强烈的免疫反应性。用层粘连蛋白或NGF预处理均未影响施万细胞的生长。然而,NGF处理增加了移植物中轴突的数量,但无法抵消损伤诱导的背根神经节中P物质的下调。结果表明,局部应用VEGF至少促进了两个在神经再生过程中很重要的事件,即施万细胞的侵入和新生血管形成。研究结果表明,生长因子预处理的作用是局部的,仅限于移植物,而诸如神经肽合成等中枢事件则不受影响。