Guillin O, Diaz J, Carroll P, Griffon N, Schwartz J C, Sokoloff P
Unité de Neurobiologie et Pharmacologie Moléculaire, INSERM U 109, Centre Paul Broca, 2ter rue d'Alésia, 75014 Paris, France.
Nature. 2001 May 3;411(6833):86-9. doi: 10.1038/35075076.
Brain-derived neurotrophic factor (BDNF), like other neurotrophins, is a polypeptidic factor initially regarded to be responsible for neuron proliferation, differentiation and survival, through its uptake at nerve terminals and retrograde transport to the cell body. A more diverse role for BDNF has emerged progressively from observations showing that it is also transported anterogradely, is released on neuron depolarization, and triggers rapid intracellular signals and action potentials in central neurons. Here we report that BDNF elicits long-term neuronal adaptations by controlling the responsiveness of its target neurons to the important neurotransmitter, dopamine. Using lesions and gene-targeted mice lacking BDNF, we show that BDNF from dopamine neurons is responsible for inducing normal expression of the dopamine D3 receptor in nucleus accumbens both during development and in adulthood. BDNF from corticostriatal neurons also induces behavioural sensitization, by triggering overexpression of the D3 receptor in striatum of hemiparkinsonian rats. Our results suggest that BDNF may be an important determinant of pathophysiological conditions such as drug addiction, schizophrenia or Parkinson's disease, in which D3 receptor expression is abnormal.
脑源性神经营养因子(BDNF)与其他神经营养因子一样,是一种多肽因子,最初被认为通过在神经末梢摄取并逆向运输到细胞体,从而负责神经元的增殖、分化和存活。随着观察结果逐渐表明BDNF也能顺向运输、在神经元去极化时释放,并在中枢神经元中触发快速的细胞内信号和动作电位,其作用变得更加多样。在此我们报告,BDNF通过控制其靶神经元对重要神经递质多巴胺的反应性,引发长期的神经元适应性变化。利用损伤模型和缺乏BDNF的基因敲除小鼠,我们发现多巴胺神经元分泌的BDNF在发育过程中和成年期均负责诱导伏隔核中多巴胺D3受体的正常表达。皮质纹状体神经元分泌的BDNF还通过触发偏侧帕金森病大鼠纹状体中D3受体的过表达,诱导行为敏化。我们的结果表明,BDNF可能是药物成瘾、精神分裂症或帕金森病等病理生理状况的重要决定因素,在这些疾病中D3受体表达异常。