Lysosomal-associated membrane protein 2 isoforms are differentially affected in early Parkinson's disease
Lysosomes are the primary catabolic compartment for the degradation of intracellular proteins through autophagy. The presence of abnormal intracellular alpha-synuclein-positive aggregates in Parkinson's disease (PD) indicates that the degradative capacity of lysosomes is impaired in PD. Specific dysfunction of chaperone-mediated autophagy (CMA) in PD is suggested by reductions in the CMA membrane receptor, lysosomal-associated membrane protein (LAMP) 2A, although whether LAMP2A is the only LAMP2 isoform affected by PD is unknown. Messenger RNA (mRNA) and protein expression of all three LAMP2 isoforms was assessed in brain extracts from regions with and without PD-related increases in alpha-synuclein in autopsy samples from subjects in the early pathological stage of PD (n = 9), compared to age- and postmortem delay-matched controls (n = 10). In the early stages of PD, mRNA expression of all LAMP2 isoforms was not different from controls, with LAMP2B and LAMP2C protein levels also unchanged in PD. The selective loss of LAMP2A protein directly correlated with the increased levels of alpha-synuclein and decreased levels of the CMA chaperone heat shock cognate protein 70 in the same PD samples, as well as with the accumulation of cytosolic CMA substrate proteins. Our data show that LAMP2 protein isoforms are differentially affected in the early stages of PD, with LAMP2A selectively reduced in association with increased alpha-synuclein, and suggests that dysregulation of CMA-mediated protein degradation occurs before substantial alpha-synuclein aggregation in PD. (c) 2015 International Parkinson and Movement Disorder Society.
|ISBN||1531-8257 (Electronic) 0885-3185 (Linking)|
|Authors||Murphy, K. E.; Gysbers, A. M.; Abbott, S. K.; Spiro, A. S.; Furuta, A.; Cooper, A.; Garner, B.; Kabuta, T.; Halliday, G. M.;|
|Publisher Name||MOVEMENT DISORDERS|
|Published Date||2015-01-01 00:00:00|
|URL link to publisher's version||http://www.ncbi.nlm.nih.gov/pubmed/25594542|
|OpenAccess link to author's accepted manuscript version||https://publications.gimr.garvan.org.au/open-access/13238|