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The prion-like nature of amyotrophic lateral sclerosis.
- Source :
-
Progress in molecular biology and translational science [Prog Mol Biol Transl Sci] 2020; Vol. 175, pp. 261-296. Date of Electronic Publication: 2020 Sep 01. - Publication Year :
- 2020
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Abstract
- The misfolding, aggregation, and deposition of specific proteins is the key hallmark of most progressive neurodegenerative disorders such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis (ALS). ALS is characterized by the rapid and progressive degenerations of motor neurons in the spinal cord and motor cortex, resulting in paralysis of those who suffer from it. Pathologically, there are three major aggregating proteins associated with ALS, including TAR DNA-binding protein of 43kDa (TDP-43), superoxide dismutase-1 (SOD1), and fused in sarcoma (FUS). While there are ALS-associated mutations found in each of these proteins, the most prevalent aggregation pathology is that of wild-type TDP-43 (97% of cases), with the remaining split between mutant forms of SOD1 (~2%) and FUS (~1%). Considering the progressive nature of ALS and its association with the aggregation of specific proteins, a growing notion is that the spread of pathology and symptoms can be explained by a prion-like mechanism. Prion diseases are a group of highly infectious neurodegenerative disorders caused by the misfolding, aggregation, and spread of a transmissible conformer of prion protein (PrP). Pathogenic PrP is capable of converting healthy PrP into a toxic form through template-directed misfolding. Application of this finding to other neurodegenerative disorders, and in particular ALS, has revolutionized our understanding of cause and progression of these disorders. In this chapter, we first provide a background on ALS pathology and genetic origin. We then detail and discuss the evidence supporting a prion-like propagation of protein misfolding and aggregation in ALS with a particular focus on SOD1 and TDP-43 as these are the most well-established models in the field.<br /> (© 2020 Elsevier Inc. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1878-0814
- Volume :
- 175
- Database :
- MEDLINE
- Journal :
- Progress in molecular biology and translational science
- Publication Type :
- Academic Journal
- Accession number :
- 32958236
- Full Text :
- https://doi.org/10.1016/bs.pmbts.2020.07.002