Centre de Biophysique Moléculaire, CNRS UPR 4301, Affiliated with the Université d'Orléans - Pôle Universitaire Centre Val de Loire, Rue Charles Sadron, 45071 Orléans Cedex 2, France.
LIFO Bat. 3IA, Université d'Orléans, Rue Léonard de Vinci, B.P. 6759F-45067 Orleans Cedex 2, France.
Gene. 2020 May 15;738:144454. doi: 10.1016/j.gene.2020.144454. Epub 2020 Feb 5.
Parkinson's disease (PD) is a common neurodegenerative disorder which affects dopaminergic neurons leading to alteration of numerous cellular pathways. Several reports highlight that PD disturbs also other cells than CNS neurons including PBMCs, which could lead, among other things, to dysfunctions of immune functions. Because autophagy could be altered in PD, a monocentric pilot study was performed to quantify the transcripts levels of several autophagy genes in blood cells. MAP1LC3B, GABARAP, GABARAPL1, GABARAPL2 and P62/SQSTM1 were found to be overexpressed in patients. On the contrary, transcripts for HSPA8 and GAPDH were both decreased. Expression of MAP1LC3B and GABARAP was able to successfully segregate PD patients from healthy controls. The accuracy of this segregation was substantially increased when combined expressions of MAP1LC3B and GAPDH or GABARAP and GAPDH were used as categorical variables. This pilot study suggests that autophagy genes expression is dysregulated in PD patients and may open new perspectives for the characterisation of prediction markers.
帕金森病(PD)是一种常见的神经退行性疾病,它会影响多巴胺能神经元,导致许多细胞途径发生改变。有几项报告强调,PD 还会干扰中枢神经系统神经元以外的其他细胞,包括 PBMCs,这可能导致免疫功能失调等问题。由于自噬在 PD 中可能会发生改变,因此进行了一项单中心试点研究,以定量检测血液细胞中几种自噬基因的转录本水平。结果发现 MAP1LC3B、GABARAP、GABARAPL1、GABARAPL2 和 P62/SQSTM1 在患者中过表达。相反,HSPA8 和 GAPDH 的转录本都减少了。MAP1LC3B 和 GABARAP 的表达能够成功地区分 PD 患者和健康对照组。当将 MAP1LC3B 和 GAPDH 或 GABARAP 和 GAPDH 的表达组合作为分类变量使用时,这种分类的准确性大大提高。这项试点研究表明,自噬基因的表达在 PD 患者中失调,这可能为预测标志物的特征描述开辟新的视角。