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Components of the Endocannabinoid and Dopamine Systems Are Dysregulated in Huntington's Disease: Analysis of Publicly Available Microarray Datasets

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Date 2015 Feb 19
PMID 25692022
Citations 3
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Abstract

The endocannabinoid system (ECS) and the dopaminergic system (DAS) are two major regulators of basal ganglia function. During Huntington's disease (HD) pathogenesis, the expression of genes in both the ECS and DAS is dysregulated. The purpose of this study was to determine the changes that were consistently observed in the ECS and DAS during HD progression in the central nervous system (CNS) and in the periphery in different models of HD and human HD tissue. To do this, we conducted a meta-analysis of differential gene expression in the ECS and DAS using publicly available microarray data. The consolidated data were summarized as observed changes in gene expression (OCGE) using a weighted sum for each gene. In addition, consolidated data were compared to previously published studies that were not available in the gene expression omnibus (GEO) database. The resulting data confirm gene expression changes observed using different approaches and provide novel insights into the consistency between changes observed in human tissue and various models, as well as disease stage- and tissue-specific transcriptional dysregulation in HD. The major implication of the systems-wide data presented here is that therapeutic strategies targeting the ECS or DAS must consider the dynamic changes in gene expression over time and in different body areas, which occur during HD progression and the interconnectedness of the two systems.

Citing Articles

Microarray profiling of hypothalamic gene expression changes in Huntington's disease mouse models.

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Huntington's disease pattern of transcriptional dysregulation in the absence of mutant huntingtin is produced by knockout of neuronal GLT-1.

Laprairie R, Petr G, Sun Y, Fischer K, Denovan-Wright E, Rosenberg P Neurochem Int. 2018; 123:85-94.

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Alpaugh M, Galleguillos D, Forero J, Morales L, Lackey S, Kar P EMBO Mol Med. 2017; 9(11):1537-1557.

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