Honma Masaru, Namikawa Kazuhiko, Mansur Khalil, Iwata Tatsuya, Mori Nozomu, Iizuka Hajime, Kiyama Hiroshi
Department of Anatomy, Asahikawa Medical College, Asahikawa, Hokkaido, Japan.
J Neurochem. 2002 Aug;82(4):961-75. doi: 10.1046/j.1471-4159.2002.01043.x.
Axotomy-induced neuronal death occurs in neonatal motoneurons, but not in adult rat. Here we demonstrated that during the course of postnatal development, nerve injury induced down-regulation of the glial cell line-derived neurotrophic factor (GDNF) receptor GFRalpha1 in axotomized hypoglossal motoneurons of rat are gradually converted to the adult up-regulation pattern of response. The compensatory expression of GFRalpha1 specifically in the injured motoneurons of neonates by adenovirus succeeded in rescuing the injured neurons without an application of growth factors. To the contrary, the nuclear antisense RNA for GFRalpha1 expression accelerates the axotomy-induced neuronal death in pups. These findings suggest that the receptor expression response after nerve injury is critical for the determination of injured motoneuron fate.
轴突切断诱导的神经元死亡发生在新生运动神经元中,但在成年大鼠中不会发生。在这里,我们证明在出生后发育过程中,大鼠舌下运动神经元轴突切断后,神经损伤诱导胶质细胞源性神经营养因子(GDNF)受体GFRα1下调,逐渐转变为成年后的上调反应模式。通过腺病毒在新生动物受损运动神经元中特异性地补偿性表达GFRα1,在不应用生长因子的情况下成功挽救了受损神经元。相反,针对GFRα1表达的核反义RNA加速了幼崽轴突切断诱导的神经元死亡。这些发现表明,神经损伤后受体表达反应对于确定受损运动神经元的命运至关重要。