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穿孔素在介导小鼠MPTP诱导的帕金森病中多巴胺能神经元损失中的作用。

Participation of perforin in mediating dopaminergic neuron loss in MPTP-induced Parkinson's disease in mice.

作者信息

Peng Su-Ping, Zhang Ye, Copray Sjef, Schachner Melitta, Shen Yan-Qin

机构信息

Center for Neuroscience, Shantou University Medical College, Shantou, Guangdong 515041, PR China; Department of Neuroscience, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.

Center for Neuroscience, Shantou University Medical College, Shantou, Guangdong 515041, PR China.

出版信息

Biochem Biophys Res Commun. 2017 Mar 11;484(3):618-622. doi: 10.1016/j.bbrc.2017.01.150. Epub 2017 Jan 28.

Abstract

Both resident innate and peripheral immune aberrations have been demonstrated to influence Parkinson's disease (PD) progression. However, it is still enigmatic how and which immune components are lethal to the dopaminergic neuron in PD. We now show that levels of perforin, a pore-forming protein expressed in cytotoxic immune cells, was significantly increased in the serum of wild-type mice 4 weeks after injection of MPTP, a toxin used to induce PD-like symptoms. We demonstrate that perforin-deficiency attenuated the acute striatal dopamine reduction by 33%, ablated microglia activation 3 days post MPTP-injection; and retarded dopaminergic neuron death 4 weeks post MPTP-injection. Our study suggests that perforin plays a role in dopaminergic neuron loss in PD.

摘要

已证实,驻留固有免疫和外周免疫异常均会影响帕金森病(PD)的进展。然而,在PD中,免疫成分如何以及哪些会对多巴胺能神经元产生致命影响仍是个谜。我们现在发现,穿孔素(一种在细胞毒性免疫细胞中表达的成孔蛋白)的水平在野生型小鼠注射MPTP(一种用于诱导类似PD症状的毒素)4周后的血清中显著升高。我们证明,穿孔素缺陷使急性纹状体多巴胺减少33%,在MPTP注射后3天消除了小胶质细胞的激活;并在MPTP注射后4周延缓了多巴胺能神经元的死亡。我们的研究表明,穿孔素在PD的多巴胺能神经元丢失中起作用。

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