The Function of Autophagy in Neurodegenerative Diseases.

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  • Author(s): Kiriyama Y;Kiriyama Y; Nochi H; Nochi H
  • Source:
    International journal of molecular sciences [Int J Mol Sci] 2015 Nov 09; Vol. 16 (11), pp. 26797-812. Date of Electronic Publication: 2015 Nov 09.
  • Publication Type:
    Journal Article; Review
  • Language:
    English
  • Additional Information
    • Source:
      Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE
    • Publication Information:
      Original Publication: Basel, Switzerland : MDPI, [2000-
    • Subject Terms:
    • Abstract:
      Macroautophagy, hereafter referred to as autophagy, is a bulk degradation process performed by lysosomes in which aggregated and altered proteins as well as dysfunctional organelles are decomposed. Autophagy is a basic cellular process that maintains homeostasis and is crucial for postmitotic neurons. Thus, impaired autophagic processes in neurons lead to improper homeostasis and neurodegeneration. Recent studies have suggested that impairments of the autophagic process are associated with several neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, and static encephalopathy of childhood with neurodegeneration in adulthood. In this review, we focus on the recent findings regarding the autophagic process and the involvement of autophagy in neurodegenerative diseases.
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    • Contributed Indexing:
      Keywords: ALS; Alzheimer’s disease; Huntington’s disease; Parkinson’s disease; SENDA; autophagy; mitophagy
    • Accession Number:
      0 (Apoptosis Regulatory Proteins)
      0 (BECN1 protein, human)
      0 (Beclin-1)
      0 (Intracellular Signaling Peptides and Proteins)
      0 (Membrane Proteins)
      0 (Multiprotein Complexes)
      EC 2.7.11.1 (Autophagy-Related Protein-1 Homolog)
      EC 2.7.11.1 (Mechanistic Target of Rapamycin Complex 1)
      EC 2.7.11.1 (Protein Serine-Threonine Kinases)
      EC 2.7.11.1 (TOR Serine-Threonine Kinases)
      EC 2.7.11.1 (ULK1 protein, human)
      EC 2.7.11.31 (AMP-Activated Protein Kinases)
    • Publication Date:
      Date Created: 20151117 Date Completed: 20160829 Latest Revision: 20220321
    • Publication Date:
      20221213
    • Accession Number:
      PMC4661849
    • Accession Number:
      10.3390/ijms161125990
    • Accession Number:
      26569220