4.7 Article

Dysfunction of the autophagy/lysosomal degradation pathway is a shared feature of the genetic synucleinopathies

Journal

FASEB JOURNAL
Volume 27, Issue 9, Pages 3424-3429

Publisher

FEDERATION AMER SOC EXP BIOL
DOI: 10.1096/fj.12-223842

Keywords

Parkinson's disease; LRRK2; GBA

Funding

  1. Michael J. Fox Foundation
  2. Parkinson's UK [F1002]
  3. Rosetrees Trust
  4. Wellcome Trust/Medical Research Council (MRC) [WT089698]
  5. Medical Research Council [MC_G1000735] Funding Source: researchfish
  6. Parkinson's UK [F-1002] Funding Source: researchfish
  7. MRC [MC_G1000735] Funding Source: UKRI

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The past decade has witnessed huge advances in our understanding of the genetics underlying Parkinson's disease. Identifying commonalities in the biological function of genes linked to Parkinson's provides an opportunity to elucidate pathways that lead to neuronal degeneration and eventually to disease. We propose that the genetic forms of Parkinson's disease largely associated with -synuclein-positive neuropathology (SNCA, LRRK2, and GBA) are brought together by involvement in the autophagy/lysosomal pathway and that this represents a unifying pathway to disease in these cases.Manzoni, C., Lewis, P. A. Dysfunction of the autophagy/lysosomal degradation pathway is a shared feature of the genetic synucleinopathies.

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