Involvement of the immune system, endocytosis and EIF2 signaling in both genetically determined and sporadic forms of Parkinson's disease

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• 作者：Eug茅nie Mutez ; Aurore Nkiliza ; Karim Belarbi ; Am茅lie de Broucker ; Christel Vanbesien-Mailliot ; S茅verine Bleuse ; Aur茅lie Duflot ; Thomas Comptdaer ; Pierre Semaille ; Renaud Blervaque ; David Hot ; Frederic Lepr锚tre ; Martin Figeac ; Alain Dest茅e ; Marie-Christine Chartier-Harlin
• 关键词：Parkinson's disease ; Transcriptome ; Peripheral blood mononuclear cell ; PBMC ; LRRK2 mutation ; Immune response ; EIF2 signaling ; Endocytosis
• 刊名：Neurobiology of Disease
• 出版年：March, 2014
• 年：2014
• 卷：63
• 期：Complete
• 页码：165-170
• 全文大小：650 K

文摘

The leucine-rich repeat kinase 2 (LRRK2) G2019S mutation is a common genetic cause of Parkinson's disease (PD). Although patients with sporadic PD and individuals with LRRK2-linked PD display the classical PD phenotype, it is not known whether or not the same biological pathways are deregulated in each context. By using transcriptome profiling, we investigated the deregulation of various biological pathways in a total of 47 peripheral blood mononuclear cell (PBMC) samples from patients with sporadic PD, patients heterozygous for the LRRK2 G2019S mutation compared to healthy controls. We found that the deregulation patterns were indeed similar in PBMCs obtained from patients with sporadic PD and from LRRK2 G2019S carriers, with dysfunctions in mitochondrial pathways, cell survival signaling, cancerization, endocytosis signaling and iron metabolism. Analysis of our PBMC data and other publicly available transcriptome datasets (for whole blood samples) showed that deregulation of the immune system, endocytosis and eukaryotic initiation factor 2 (EIF2) signaling are the main features of transcriptome profiles in PD (since they are also present in the transcriptome of dopaminergic neurons from patients). Transcriptome analysis of PBMCs is thus valuable for (i) characterizing the pathophysiological pathways shared by genetic and sporadic forms of PD and (ii) identifying potential biomarkers and therapeutic targets. This minimally invasive approach opens up tremendous perspectives for better diagnosis and therapy of neurodegenerative diseases because it can be applied from the earliest stages of the disease onwards.