Lysosomal-associated membrane protein 2 isoforms are differentially affected in early Parkinson's disease

Mov Disord. 2015 Oct;30(12):1639-47. doi: 10.1002/mds.26141. Epub 2015 Jan 16.

Abstract

Lysosomes are the primary catabolic compartment for the degradation of intracellular proteins through autophagy. The presence of abnormal intracellular α-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 α-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 α-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 α-synuclein, and suggests that dysregulation of CMA-mediated protein degradation occurs before substantial α-synuclein aggregation in PD.

Keywords: LAMP2; Parkinson's disease; chaperone-mediated autophagy (CMA); nucleic acid autophagy; α-synuclein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Brain / metabolism
  • Cholesterol / metabolism
  • Female
  • HSP70 Heat-Shock Proteins / genetics
  • HSP70 Heat-Shock Proteins / metabolism
  • Humans
  • Lipid Metabolism
  • Lysosomal-Associated Membrane Protein 2 / genetics
  • Lysosomal-Associated Membrane Protein 2 / metabolism*
  • Male
  • Middle Aged
  • Parkinson Disease / metabolism*
  • Parkinson Disease / pathology*
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism*
  • RNA, Messenger / metabolism
  • Statistics, Nonparametric
  • alpha-Synuclein / genetics
  • alpha-Synuclein / metabolism

Substances

  • HSP70 Heat-Shock Proteins
  • Lysosomal-Associated Membrane Protein 2
  • Protein Isoforms
  • RNA, Messenger
  • alpha-Synuclein
  • Cholesterol