Hallett Penelope J, Cooper Oliver, Sadi Damaso, Robertson Harold, Mendez Ivar, Isacson Ole
Neuroregeneration Research Institute, Harvard University and McLean Hospital, 115 Mill Street, Belmont, MA 02478, USA.
Division of Neurosurgery, Department of Anatomy and Neurobiology, and Department of Pharmacology, Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, NS B3H 3A7, Canada.
Cell Rep. 2014 Jun 26;7(6):1755-61. doi: 10.1016/j.celrep.2014.05.027. Epub 2014 Jun 6.
To determine the long-term health and function of transplanted dopamine neurons in Parkinson's disease (PD) patients, the expression of dopamine transporters (DATs) and mitochondrial morphology were examined in human fetal midbrain cellular transplants. DAT was robustly expressed in transplanted dopamine neuron terminals in the reinnervated host putamen and caudate for at least 14 years after transplantation. The transplanted dopamine neurons showed a healthy and nonatrophied morphology at all time points. Labeling of the mitochondrial outer membrane protein Tom20 and α-synuclein showed a typical cellular pathology in the patients' own substantia nigra, which was not observed in transplanted dopamine neurons. These results show that the vast majority of transplanted neurons remain healthy for the long term in PD patients, consistent with clinical findings that fetal dopamine neuron transplants maintain function for up to 15-18 years in patients. These findings are critically important for the rational development of stem-cell-based dopamine neuronal replacement therapies for PD.
为了确定帕金森病(PD)患者中移植的多巴胺神经元的长期健康状况和功能,研究人员在人胎儿中脑细胞移植中检测了多巴胺转运体(DATs)的表达和线粒体形态。移植后至少14年,DAT在重新支配的宿主壳核和尾状核的移植多巴胺神经元终末中强烈表达。在所有时间点,移植的多巴胺神经元均显示出健康且未萎缩的形态。线粒体外膜蛋白Tom20和α-突触核蛋白的标记显示患者自身黑质中存在典型的细胞病理学变化,而在移植的多巴胺神经元中未观察到这种情况。这些结果表明,在PD患者中,绝大多数移植神经元长期保持健康,这与胎儿多巴胺神经元移植在患者体内维持功能长达15至18年的临床发现一致。这些发现对于合理开发基于干细胞的PD多巴胺神经元替代疗法至关重要。