Dysregulation of gene expression in a lysosomal storage disease varies between brain regions implicating unexpected mechanisms of neuropathology.

Abstract

The characteristic neurological feature of many neurogenetic diseases is intellectual disability. Although specific neuropathological features have been described, the mechanisms by which specific gene defects lead to cognitive impairment remain obscure. To gain insight into abnormal functions occurring secondary to a single gene defect, whole transcriptome analysis was used to identify molecular and cellular pathways that are dysregulated in the brain in a mouse model of a lysosomal storage disorder (LSD) (mucopolysaccharidosis [MPS] VII). We assayed multiple anatomical regions separately, in a large cohort of normal and diseased mice, which greatly increased the number of significant changes that could be detected compared to past studies in LSD models. We found that patterns of aberrant gene expression and involvement of multiple molecular and cellular systems varied significantly between brain regions. A number of changes revealed unexpected system and process alterations, such as up-regulation of the immune system with few inflammatory changes (a significant difference from the closely related MPS IIIb model), down-regulation of major oligodendrocyte genes even though white matter changes are not a feature histopathologically, and a plethora of developmental gene changes. The involvement of multiple neural systems indicates that the mechanisms of neuropathology in this type of disease are much broader than previously appreciated. In addition, the variation in gene dysregulation between brain regions indicates that different neuropathologic mechanisms may predominate within different regions of a diseased brain caused by a single gene mutation.

• Authors: Michael K Parente, Ramona Rozen, Cassia N Cearley, John H Wolfe
• Journal: PloS one (PLoS One) Vol. 7 Issue 3 Pg. e32419 ( 2012) ISSN: 1932-6203 [Electronic] United States
• PMID: 22403656 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Ion Channels

Topics

• Animals
• Brain (cytology, immunology, metabolism, pathology)
• Cell Adhesion (genetics)
• Cell Cycle (genetics)
• Cell Nucleus (genetics)
• Circadian Rhythm (genetics)
• Extracellular Matrix (metabolism)
• Female
• Gliosis (genetics, metabolism, pathology)
• Ion Channels (metabolism)
• Male
• Mice
• Microglia (metabolism, pathology)
• Mucopolysaccharidosis VII (genetics, immunology, metabolism, pathology)
• Myelin Sheath (physiology)
• Neurons (metabolism, pathology)
• Olfactory Bulb (pathology)
• Signal Transduction (genetics)
• Transcriptome