Ontology highlight
ABSTRACT: Background
Mutant huntingtin (mHTT) is encoded by the Huntington's disease (HD) gene and its accumulation in the brain contributes to HD pathogenesis. Reducing mHTT levels through activation of the autophagosome-lysosomal pathway may have therapeutic benefit. Transcription factor EB (TFEB) regulates lysosome biogenesis and autophagy.Objective
To examine if increasing TFEB protein levels in HD mouse striatum induces autophagy and influences mHTT levels.Methods
We introduced cDNA encoding TFEB with an HA tag (TFEB-HA) under the control of neuron specific synapsin 1 promoter into the striatum of 3 month old HDQ175/Q7 mice using adeno-associated virus AAV2/9. The levels of exogenous TFEB were analyzed using qPCR and Western blot. Proteins involved in autophagy, levels of huntingtin, and striatal-enriched proteins were examined using biochemical and/or immunohistochemical methods.Results
In HD mice expressing TFEB-HA, HA immunoreactivity distributed throughout the striatum in neuronal cell bodies and processes and preferentially in neuronal nuclei and overlapped with a loss of DARPP32 immunoreactivity. TFEB-HA mRNA and protein were detected in striatal lysates. There were increased levels of proteins involved with autophagosome/lysosome activity including LAMP-2A, LC3II, and cathepsin D and reduced levels of mutant HTT and the striatal enriched proteins DARPP32 and PDE10A. Compared to WT mice, HDQ175/Q7 mice had elevated levels of the ER stress protein GRP78/BiP and with TFEB-HA expression, increased levels of the astrocyte marker GFAP and pro-caspase 3.Conclusion
These results suggest that TFEB expression in the striatum of HDQ175/Q7 mice stimulates autophagy and lysosome activity, and lowers mHTT, but may also increase a neuronal stress response.
SUBMITTER: Vodicka P
PROVIDER: S-EPMC5088406 | biostudies-literature | 2016 Oct
REPOSITORIES: biostudies-literature
Vodicka Petr P Chase Kathryn K Iuliano Maria M Tousley Adelaide A Valentine Dana T DT Sapp Ellen E Kegel-Gleason Kimberly B KB Sena-Esteves Miguel M Aronin Neil N DiFiglia Marian M
Journal of Huntington's disease 20161001 3
<h4>Background</h4>Mutant huntingtin (mHTT) is encoded by the Huntington's disease (HD) gene and its accumulation in the brain contributes to HD pathogenesis. Reducing mHTT levels through activation of the autophagosome-lysosomal pathway may have therapeutic benefit. Transcription factor EB (TFEB) regulates lysosome biogenesis and autophagy.<h4>Objective</h4>To examine if increasing TFEB protein levels in HD mouse striatum induces autophagy and influences mHTT levels.<h4>Methods</h4>We introduce ...[more]