Yamada Yoshihisa, Shimizu Katsuji, Nitta Atsumi, Soumiya Hitomi, Fukumitsu Hidefumi, Furukawa Shoei
Laboratory of Molecular Biology, Gifu Pharmaceutical University, Mitahora-higashi, Japan.
Neurosci Lett. 2004 Jun 24;364(1):11-5. doi: 10.1016/j.neulet.2004.03.078.
The effect of axonal regeneration on de novo synthesis of glial cell line-derived neurotrophic factor (GDNF) in rat sciatic nerves was examined. Transection of the sciatic nerve caused a prominent increase in the GDNF content in the distal segments within 1 week. The high level was sustained until 4 weeks in the animal model in which the nerve ends were ligated with thread (non-regeneration group); however, it was reduced to the original level within 2 or 4 weeks after the transection only in the segments invaded by regenerating axons in the models in which the nerve ends were coaptated (regeneration group). Expression of both GDNF protein and mRNA was decreased with a reciprocal increase in the density of neurofilaments, used as a marker of axonal ingrowth in distal segments of the regeneration group, suggesting that axonal contact turned off the GDNF-mediated nerve regeneration activity.
研究了轴突再生对大鼠坐骨神经中胶质细胞源性神经营养因子(GDNF)从头合成的影响。坐骨神经横断后1周内,远段GDNF含量显著增加。在神经末端用线结扎的动物模型(非再生组)中,高水平一直维持到4周;然而,在神经末端吻合的模型(再生组)中,仅在再生轴突侵入的节段,横断后2周或4周内GDNF含量降至原始水平。再生组远段中作为轴突长入标志物的神经丝密度呈反比增加,同时GDNF蛋白和mRNA的表达均降低,提示轴突接触关闭了GDNF介导的神经再生活性。