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Autophagy and apoptosis dysfunction in neurodegenerative disorders
Open accessAbstract
Autophagy and apoptosis are basic physiologic processes contributing to the maintenance of cellular homeostasis. Autophagy encompasses pathways that target long-lived cytosolic proteins and damaged organelles. It involves a sequential set of events including double membrane formation, elongation, vesicle maturation and finally delivery of the targeted materials to the lysosome. Apoptotic cell death is best described through its morphology. It is characterized by cell rounding, membrane blebbing, cytoskeletal collapse, cytoplasmic condensation, and fragmentation, nuclear pyknosis, chromatin condensation/fragmentation, and formation of membrane-enveloped apoptotic bodies, that are rapidly phagocytosed by macrophages or neighboring cells. Neurodegenerative disorders are becoming increasingly prevalent, especially in the Western societies, with larger percentage of members living to an older age. They have to be seen not only as a health problem, but since they are care-intensive, they also carry a significant economic burden. Deregulation of autophagy plays a pivotal role in the etiology and/or progress of many of these diseases. Herein, we briefly review the latest findings that indicate the involvement of autophagy in neurodegenerative diseases. We provide a brief introduction to autophagy and apoptosis pathways focusing on the role of mitochondria and lysosomes. We then briefly highlight pathophysiology of common neurodegenerative disorders like Alzheimer's diseases, Parkinson's disease, Huntington's disease and Amyotrophic lateral sclerosis. Then, we describe functions of autophagy and apoptosis in brain homeostasis, especially in the context of the aforementioned disorders. Finally, we discuss different ways that autophagy and apoptosis modulation may be employed for therapeutic intervention during the maintenance of neurodegenerative disorders.
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“For example, some “neurodevelopmental” disorders can present later in the teens to early adulthood, while early-onset “neurodegenerative” disorders can be seen in the 4th or 5th decade of life.”
From The lysosome and proteostatic stress at the intersection of pediatric neurological disorders and adult neurodegenerative diseases (2025) · cites this paper as [63]
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“However, PCD is increasingly implicated in several aging-associated neurodegenerative diseases(Ghavami et al., 2014).”
From Programmed cell death in aging (2015) · cites this paper as Ghavami et al., 2014
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“It can present in adulthood, quite late for a neurodevelopmental disorder.62,63”
From The lysosome and proteostatic stress at the intersection of pediatric neurological disorders and adult neurodegenerative diseases (2025) · cites this paper as [63]
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“A striking example of this overlap is Kufor-Rakeb syndrome, an autosomal recessive early-onset form of Parkinson’s disease caused by mutations in the lysosomal ATPase protein, ATP13A2.”
From The lysosome and proteostatic stress at the intersection of pediatric neurological disorders and adult neurodegenerative diseases (2025) · cites this paper as [63]
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“The data suggest that a disruption of normal autophagy/mitophagy may contribute to mitochondrial malfunction and thereby promote PCD (Ghavami et al., 2014; Hroudova et al., 2014; Nixon and Yang, 2012).”
From Programmed cell death in aging (2015) · cites this paper as Ghavami et al., 2014
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Metadata
- Authors
- Ghavami, S., Shojaei, S., Yeganeh, B., Ande, S. R., Jangamreddy, J. R., Mehrpour, M., Christoffersson, J., Chaabane, W., Moghadam, A. R., Kashani, H. H., Hashemi, M., Owji, A. A., & Łos, M. J.
- Affiliations
- Children's Hospital Research Institute of Manitoba (CA)
- Shiraz University of Medical Sciences (IR)
- University of Toronto (CA)
- University of Manitoba (CA)
- Linköping University (SE)
- Inserm (FR)
- Islamic Azad University Ardabil (IR)
- Zahedan University of Medical Sciences (IR)
- Corresponding author
- Owji, Ali A.
- ORCID
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2014-01
- Volume
- 112
- Pages
- 24-49
- ISSN
- 0301-0082 (ISSN-L)
- OpenAlex
- W2125461230
- Cited by
- 1,039
- References
- 387
- Citations by year
- 2026: 31 · 2025: 56 · 2024: 90 · 2023: 78 · 2022: 87 · 2021: 112 · 2020: 110 · 2019: 102 · 2018: 86 · 2017: 72 · 2016: 93 · 2015: 81 · 2014: 39
- FWCI
- 8.45
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Progress in Neurobiology (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- KTH Publication Database DiVA (KTH Royal Institute of Technology) (submittedVersion, other-oa)
- Funders
- Manitoba Health Research Council
- Cancerfonden
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- autophagy, apoptosis, neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, mitochondria, lysosomes, brain homeostasis, autophagy modulation, therapeutic interventions
- MeSH terms
- Animals, Autophagy, Brain, Brain Diseases, Humans, Neurons, Peripheral Nervous System Diseases, Apoptosis, Neurodegenerative Diseases
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