Müller Janine, Ossig Christiana, Greiner Johannes F W, Hauser Stefan, Fauser Mareike, Widera Darius, Kaltschmidt Christian, Storch Alexander, Kaltschmidt Barbara
Molecular Neurobiology, University of Bielefeld, Bielefeld, Germany; Division of Neurodegenerative Diseases, Department of Neurology, and Center for Regenerative Therapies Dresden, Dresden University of Technology, Dresden, Germany; German Center for Neurodegenerative Diseases Dresden, Dresden, Germany; Cell Biology, University of Bielefeld, Bielefeld, Germany.
Molecular Neurobiology, University of Bielefeld, Bielefeld, Germany; Division of Neurodegenerative Diseases, Department of Neurology, and Center for Regenerative Therapies Dresden, Dresden University of Technology, Dresden, Germany; German Center for Neurodegenerative Diseases Dresden, Dresden, Germany; Cell Biology, University of Bielefeld, Bielefeld, Germany
Stem Cells Transl Med. 2015 Jan;4(1):31-43. doi: 10.5966/sctm.2014-0078. Epub 2014 Dec 5.
Parkinson's disease (PD) is considered the second most frequent and one of the most severe neurodegenerative diseases, with dysfunctions of the motor system and with nonmotor symptoms such as depression and dementia. Compensation for the progressive loss of dopaminergic (DA) neurons during PD using current pharmacological treatment strategies is limited and remains challenging. Pluripotent stem cell-based regenerative medicine may offer a promising therapeutic alternative, although the medical application of human embryonic tissue and pluripotent stem cells is still a matter of ethical and practical debate. Addressing these challenges, the present study investigated the potential of adult human neural crest-derived stem cells derived from the inferior turbinate (ITSCs) transplanted into a parkinsonian rat model. Emphasizing their capability to give rise to nervous tissue, ITSCs isolated from the adult human nose efficiently differentiated into functional mature neurons in vitro. Additional successful dopaminergic differentiation of ITSCs was subsequently followed by their transplantation into a unilaterally lesioned 6-hydroxydopamine rat PD model. Transplantation of predifferentiated or undifferentiated ITSCs led to robust restoration of rotational behavior, accompanied by significant recovery of DA neurons within the substantia nigra. ITSCs were further shown to migrate extensively in loose streams primarily toward the posterior direction as far as to the midbrain region, at which point they were able to differentiate into DA neurons within the locus ceruleus. We demonstrate, for the first time, that adult human ITSCs are capable of functionally recovering a PD rat model.
帕金森病(PD)被认为是第二常见且最严重的神经退行性疾病之一,伴有运动系统功能障碍以及抑郁和痴呆等非运动症状。使用当前的药物治疗策略来补偿帕金森病期间多巴胺能(DA)神经元的渐进性丧失是有限的,并且仍然具有挑战性。基于多能干细胞的再生医学可能提供一种有前景的治疗选择,尽管人类胚胎组织和多能干细胞的医学应用仍然是一个伦理和实际争议的问题。为应对这些挑战,本研究调查了源自下鼻甲的成人神经嵴衍生干细胞(ITSCs)移植到帕金森病大鼠模型中的潜力。强调其产生神经组织的能力,从成人鼻子分离的ITSCs在体外有效分化为功能性成熟神经元。ITSCs随后成功地向多巴胺能分化,然后将其移植到单侧损伤的6-羟基多巴胺大鼠帕金森病模型中。预分化或未分化的ITSCs移植导致旋转行为的强劲恢复,同时黑质内的DA神经元显著恢复。ITSCs进一步显示在松散的溪流中广泛迁移,主要向后方向延伸至中脑区域,此时它们能够在蓝斑内分化为DA神经元。我们首次证明,成人ITSCs能够在功能上恢复帕金森病大鼠模型。