4.6 Review

Autophagy-Lysosomal Pathway as Potential Therapeutic Target in Parkinson's Disease

Journal

CELLS
Volume 10, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/cells10123547

Keywords

autophagy; lysosomes; neurodegenerative disease; Parkinson's disease; autoimmunity

Categories

Funding

  1. French National Centre for Scientific Research (CNRS)
  2. Region Grand-Est
  3. University of Strasbourg Institute for Advanced Study (USIAS)
  4. Interdisciplinary Thematic Institute 2021-2028 program of the University of Strasbourg, Inserm [ANR-10-IDEX-0002, ANR-20-SFRI-0012]
  5. TRANSAUTOPHAGY COST Action [CA15138]
  6. French-language autophagy club (CFATG)
  7. European Regional Development Fund of the European Union
  8. Interdisciplinary Thematic Institute 2021-2028 program of the University of Strasbourg, CNRS [ANR-10-IDEX-0002, ANR-20-SFRI-0012]

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Cellular quality control systems, particularly autophagy, play a crucial role in cell survival and maintaining homeostasis. Different types of autophagy pathways show varying degrees of selectivity towards substrates. In neurodegenerative diseases, such as Parkinson's disease, autophagy is important and therapeutic strategies targeting autophagy may alter disease progression.
Cellular quality control systems have gained much attention in recent decades. Among these, autophagy is a natural self-preservation mechanism that continuously eliminates toxic cellular components and acts as an anti-ageing process. It is vital for cell survival and to preserve homeostasis. Several cell-type-dependent canonical or non-canonical autophagy pathways have been reported showing varying degrees of selectivity with regard to the substrates targeted. Here, we provide an updated review of the autophagy machinery and discuss the role of various forms of autophagy in neurodegenerative diseases, with a particular focus on Parkinson's disease. We describe recent findings that have led to the proposal of therapeutic strategies targeting autophagy to alter the course of Parkinson's disease progression.

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