Arias-Carrión Oscar, Drucker-Colín René, Murillo-Rodríguez Eric
Depto. de Neurociencias/Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Circuito Interior, Ciudad Universitaria, México DF, México.
Neurosci Lett. 2006 Aug 14;404(1-2):93-7. doi: 10.1016/j.neulet.2006.05.017. Epub 2006 Jun 9.
Narcolepsy is a sleep disorder characterized by excessive daytime sleepiness, inadvertent transitions from wakefulness to rapid eye movement sleep (so called "sleep-onset REMS period") and cataplexy (sudden bilateral skeletal muscle weakness during waking without impairment of consciousness). This disorder has been recently linked to a loss of hypocretin (HCRT) neurons making narcolepsy a neurodegenerative disease. Neuronal replacement could be used to reverse the symptoms of narcolepsy. Towards this end, we have recently reported that HCRT neurons from rat pups can survive when grafted into the pons of adult rats. Here, we investigate the time-course of survival of grafted HCRT neurons into the pons of adult rats. The HCRT neurons are present only in the lateral hypothalamus, and therefore suspension of cells from this region was derived from 8- to 10-day-old rat pups (donor), and grafted into the pons of adult (60 days old) host rats. Control rats received a transplant that consisted of cells from the cerebellum where no HCRT neurons are present. All adult host rats were sacrificed 1, 3, 6, 9, 12, 24, or 36 days after grafting. Immunohistochemistry was used to identify and count the presence of the HCRT grafted neurons in the target area. The tally of HCRT neurons present in the graft zone 1 day post-grafting was considered to be the baseline. From day 3 to 36 post-transplant there was a steady decline in the number of HCRT neurons. We also noted that on day 36, the HCRT neurons that survived in the pons had morphological features that were similar to mature HCRT neurons in the adult lateral hypothalamus, suggesting that these neurons might be functionally active. Control rats that received grafts of cerebellar tissue did not show HCRT neurons in the target area. These results demonstrate that there is a progressive decline in the number of transplanted neurons, but a significant percentage of HCRT neurons do survive until day 36. This study highlights the potential use of transplants as a therapeutical tool in order to treat narcolepsy.
发作性睡病是一种睡眠障碍,其特征为日间过度嗜睡、从清醒状态不经意地过渡到快速眼动睡眠(即所谓的“睡眠始发快速眼动期”)以及猝倒(清醒时双侧骨骼肌突然无力,但意识不受损害)。这种疾病最近被认为与下丘泌素(HCRT)神经元缺失有关,从而使发作性睡病成为一种神经退行性疾病。神经元替代疗法可用于逆转发作性睡病的症状。为此,我们最近报道,将大鼠幼崽的HCRT神经元移植到成年大鼠脑桥后能够存活。在此,我们研究移植到成年大鼠脑桥的HCRT神经元的存活时间进程。HCRT神经元仅存在于下丘脑外侧,因此该区域的细胞悬液取自8至10日龄的大鼠幼崽(供体),并移植到成年(60日龄)宿主大鼠的脑桥中。对照大鼠接受的移植由不存在HCRT神经元的小脑细胞组成。所有成年宿主大鼠在移植后1、3、6、9、12、24或36天被处死。采用免疫组织化学方法鉴定并计数移植到目标区域的HCRT神经元数量。移植后1天移植区中存在的HCRT神经元数量被视为基线。移植后第3天至第36天,HCRT神经元数量持续下降。我们还注意到,在第36天,存活于脑桥中的HCRT神经元具有与成年下丘脑外侧成熟HCRT神经元相似的形态特征,这表明这些神经元可能具有功能活性。接受小脑组织移植的对照大鼠在目标区域未显示HCRT神经元。这些结果表明,移植神经元数量呈逐渐下降趋势,但相当比例的HCRT神经元确实存活至第36天。这项研究凸显了移植作为治疗发作性睡病的治疗工具的潜在用途。