Distinct Stress Response and Altered Striatal Transcriptome in Alpha-Synuclein Overexpressing Mice

• Published in: Frontiers in neuroscience 2019-01, Vol.12, p.1033-1033
• Main Authors: Wassouf, Zinah, Hentrich, Thomas, Casadei, Nicolas, Jaumann, Mirko, Knipper, Marlies, Riess, Olaf, Schulze-Hentrich, Julia M
• Format: Article
• Language: English
• Subjects: Age; alpha-synuclein; Anxiety; Artificial chromosomes; Behavior; chronic unpredictable mild stress; Cortisol; Dementia; Disease; Environmental stress; Gene expression; Genomics; Genotypes; Hippocampus; Hormones; Inflammation; Mental disorders; Metabolites; Mimicry; Motor skill; Movement disorders; Mutation; Neostriatum; Neurodegeneration; Neurodegenerative diseases; Neuroscience; Parkinson's disease; Pathology; psychiatric-related behavior; Stress; Stress response; Synuclein; transcriptome
• ISSN: 1662-4548; 1662-453X; 1662-453X
• DOI: 10.3389/fnins.2018.01033

Parkinson's disease (PD) is a progressive neurodegenerative disorder with motor symptoms and a plethora of non-motor and neuropsychiatric features that accompany the disease from prodromal to advanced stages. While several genetic defects have been identified in familial forms of PD, the predominance of cases are sporadic and result from a complex interplay of genetic and non-genetic factors. Clinical evidence, moreover, indicates a role of environmental stress in PD, supported by analogies between stress-induced pathological consequences and neuronal deterioration observed in PD. From this perspective, we set out to investigate the effects of chronic stress exposure in the context of PD by using a genetic mouse model that overexpresses human wildtype . Mimicking chronic stress was achieved by adapting a chronic unpredictable mild stress protocol (CUMS) comprising eight different stressors that were applied randomly over a period of eight weeks starting at an age of four months. A distinctive stress response with an impact on anxiety-related behavior was observed upon overexpression and CUMS exposure. -overexpressing mice showed prolonged elevation of cortisol metabolites during CUMS exposure, altered anxiety-related traits, and declined motor skills surfacing with advanced age. To relate our phenotypic observations to molecular events, we profiled the striatal and hippocampal transcriptome and used a 2 × 2 factorial design opposing genotype and environment to determine differentially expressed genes. Disturbed striatal gene expression and minor hippocampal gene expression changes were observed in -overexpressing mice at six months of age. Irrespective of the CUMS-exposure, genes attributed to the terms neuroinflammation, Parkinson's signaling, and plasticity of synapses were altered in the striatum of -overexpressing mice.