Pittsburgh Institute for Neurodegenerative Diseases and Center for Neuroscience, University of Pittsburgh, PA, USA.
Brain Res. 2011 Jan 25;1370:80-8. doi: 10.1016/j.brainres.2010.11.006. Epub 2010 Nov 6.
Glial cell line-derived neurotrophic factor (GDNF) protects dopamine (DA) neurons from 6-hydroxydopamine (6-OHDA) toxicity. We have now explored this protection over 8 weeks following toxin administration. Infusion of Fluoro-Gold (FG) into the striatum was followed 1 week later by GDNF (9μg) or its vehicle. Six hours later, animals received 6-OHDA (4 μg) into the same site. 6-OHDA caused a loss of cells in the substantia nigra that expressed both FG and tyrosine hydroxylase (TH) and striatal terminals expressing TH, the high affinity dopamine transporter (DAT), and the vesicular monoamine transporter 2 (VMAT2) as assessed 2-8 weeks later. Loss of FG(+) cells, and striatal DA was completely blocked by GDNF by 2 weeks. In contrast, GDNF only slightly attenuated the loss of TH, DAT, or VMAT2 in the striatum at 2 weeks, but had restored these markers by 4-8 weeks. Thus, GDNF prevents DA cell death and loss of striatal DA content, but several weeks are required to fully restore the dopaminergic phenotype. These results provide insight into the mechanism of GDNF protection of DA neurons, and may help avoid incorrect interpretations of temporary phenotypic changes.
胶质细胞源性神经营养因子(GDNF)可保护多巴胺(DA)神经元免受 6-羟多巴胺(6-OHDA)毒性的侵害。我们现在已经在毒素给药后 8 周内探索了这种保护作用。将荧光金(FG)注入纹状体 1 周后,再注入 GDNF(9μg)或其载体。6 小时后,动物在同一部位接受 6-OHDA(4μg)。6-OHDA 导致表达 FG 和酪氨酸羟化酶(TH)的黑质细胞以及表达 TH、高亲和力多巴胺转运体(DAT)和囊泡单胺转运体 2(VMAT2)的纹状体末端的细胞丧失,在 2-8 周后进行评估。2 周时,GDNF 完全阻断了 FG(+)细胞和纹状体 DA 的丧失。相比之下,GDNF 仅在 2 周时轻微减轻了纹状体中 TH、DAT 或 VMAT2 的丧失,但在 4-8 周时已恢复了这些标志物。因此,GDNF 可防止 DA 神经元死亡和纹状体 DA 含量丧失,但需要数周时间才能完全恢复多巴胺能表型。这些结果提供了对 GDNF 保护 DA 神经元机制的深入了解,并可能有助于避免对暂时表型变化的错误解释。