Experimental Neurology, Philipps University, D-35033 Marburg, Germany.
Med Hypotheses. 2009 Nov;73(5):757-9. doi: 10.1016/j.mehy.2009.04.029. Epub 2009 May 24.
The clinical motor dysfunction in Parkinson s disease (PD) is primarily linked to the depletion of dopamine in the striatum consecutive to the loss of the large dopaminergic neurons in the substantia nigra. Despite intense investigations, no effective therapy is available to prevent the onset, or to halt the progression of the neuronal cell loss. Here, we hypothesize that autologous adult neural stem cells (NSCs) are an attractive source for cell therapy to treat PD. They overcome the ethical issues inherent to the use of human fetal tissue or embryonic stem cells. NSCs derived from adult tissue also open the possibility for autologous transplantation, where NSCs are taken out from the patient, expanded and differentiated in vitro and re-implanted back as dopaminergic precursor cells.
帕金森病(PD)的临床运动功能障碍主要与纹状体中多巴胺的耗竭有关,这是由于黑质中大型多巴胺能神经元的丧失。尽管进行了深入的研究,但目前尚无有效的治疗方法可以预防疾病的发生,或阻止神经元细胞丢失的进展。在这里,我们假设自体成体神经干细胞(NSCs)是治疗 PD 的细胞治疗的有吸引力的来源。它们克服了使用人胎儿组织或胚胎干细胞所固有的伦理问题。来自成人组织的 NSCs 还为自体移植开辟了可能性,即从患者体内取出 NSCs,在体外扩增和分化,然后作为多巴胺能前体细胞再植入体内。