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Comment
. 2013 Feb 26;110(9):3214-5.
doi: 10.1073/pnas.1300822110. Epub 2013 Feb 14.

Glucocerebrosidase in the pathogenesis and treatment of Parkinson disease

Affiliations
Comment

Glucocerebrosidase in the pathogenesis and treatment of Parkinson disease

Anthony H V Schapira et al. Proc Natl Acad Sci U S A. .
No abstract available

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Fig. 1.
Fig. 1.
The glucocerebrosidase/SNCA axis, potential targets for therapeutic intervention for PD. SNCA interacts with both wild-type (WT) and mutant (Mut) GCase, and modulation of this may serve to reduce SNCA concentrations and delay or reverse PD-related pathology. Strategies to increase lysosomal GCase or to decrease extralysosomal GCase–SNCA interactions would be anticipated to reduce SNCA concentrations. Chaperones, histone deacetylase inhibitors [HDACi), or increased expression of GCase by, for example, gene therapy (AAV-GBA) may be examples of such strategies.

Comment on

References

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