Arias-Carrión Oscar, Hernández-López Salvador, Ibañez-Sandoval Osvaldo, Bargas José, Hernández-Cruz Arturo, Drucker-Colín René
Departamento de Neurociencias, Instituto de Fisiología Celular,Universidad Nacional Autónoma de México, México City, México.
J Neurosci Res. 2006 Nov 15;84(7):1425-37. doi: 10.1002/jnr.21068.
Neurogenesis in the adult mammalian brain continues in the subventricular zone (SVZ). Neuronal precursors from the SVZ migrate along the rostral migratory stream to replace olfactory bulb interneurons. After the destruction of the nigro-striatal pathway (SN-lesion), some SVZ precursors begin to express tyrosine hydroxylase (TH) and neuronal markers (NeuN). Grafting of chromaffin cells (CCs) into the denervated striatum increases the number of TH+ cells (SVZ TH+ cells; Arias-Carrión et al., 2004). This study examines the functional properties of these newly differentiating TH+ cells. Under whole-cell patch-clamp, most SVZ cells recorded from lesioned and grafted animals (either TH+ or TH-) were non-excitable. Nevertheless, a small percentage of SVZ TH+ cells had the electrophysiologic phenotype of mature dopaminergic neurons and showed spontaneous postsynaptic potentials. Dopamine (DA) release was measured in SVZ and striatum from both control and SN-lesioned rats. As expected, 12 weeks after SN lesion, DA release decreased drastically. Nevertheless, 8 weeks after CCs graft, release from the SVZ of SN-lesioned rats recovered, and even surpassed that from control SVZ, suggesting that newly formed SVZ TH+ cells release DA. This study shows for the first time that in response to SN-lesions and CC grafts neural precursors within the SVZ change their developmental program, by not only expressing TH, but more importantly by acquiring excitable properties of mature dopaminergic neurons. Additionally, the release of DA in a Ca(2+)-dependent manner and the attraction of synaptic afferents from neighboring neuronal networks gives further significance to the overall findings, whose potential importance is discussed.
成年哺乳动物大脑中的神经发生在脑室下区(SVZ)持续进行。来自SVZ的神经元前体细胞沿着吻侧迁移流迁移,以替代嗅球中间神经元。黑质-纹状体通路破坏(SN损伤)后,一些SVZ前体细胞开始表达酪氨酸羟化酶(TH)和神经元标志物(NeuN)。将嗜铬细胞(CCs)移植到去神经支配的纹状体中可增加TH+细胞的数量(SVZ TH+细胞;Arias-Carrión等人,2004年)。本研究考察了这些新分化的TH+细胞的功能特性。在全细胞膜片钳记录下,从损伤和移植动物中记录到的大多数SVZ细胞(TH+或TH-)都不具有兴奋性。然而,一小部分SVZ TH+细胞具有成熟多巴胺能神经元的电生理表型,并表现出自发的突触后电位。在对照大鼠和SN损伤大鼠的SVZ和纹状体中测量了多巴胺(DA)释放。正如预期的那样,SN损伤12周后,DA释放急剧下降。然而,CCs移植8周后,SN损伤大鼠SVZ的释放恢复,甚至超过了对照SVZ的释放,这表明新形成的SVZ TH+细胞释放DA。本研究首次表明,响应SN损伤和CCs移植,SVZ内的神经前体细胞改变了它们的发育程序,不仅表达TH,更重要的是获得了成熟多巴胺能神经元的兴奋性特性。此外,DA以Ca(2+)依赖的方式释放以及来自相邻神经网络的突触传入的吸引赋予了整体研究结果更多意义,文中讨论了其潜在的重要性。