An Update on Autophagy in Prion Diseases

López-Pérez, O. ; Badiola, J.J. (Universidad de Zaragoza) ; Bolea, R. (Universidad de Zaragoza) ; Ferrer, I. ; Llorens, F. ; Martín-Burriel, I. (Universidad de Zaragoza)
An Update on Autophagy in Prion Diseases
Resumen: Autophagy is a dynamic intracellular mechanism involved in protein and organelle turnover through lysosomal degradation. When properly regulated, autophagy supports normal cellular and developmental processes, whereas defects in autophagic degradation have been associated with several pathologies, including prion diseases. Prion diseases, or transmissible spongiform encephalopathies (TSE), are a group of fatal neurodegenerative disorders characterized by the accumulation of the pathological misfolded isoform (PrPSc) of the physiological cellular prion protein (PrPc) in the central nervous system. Autophagic vacuoles have been described in experimental models of TSE and in the natural disease in humans. The precise connection of this process with prion-related neuropathology, or even whether autophagy is completely beneficial or pathogenic during neurodegeneration, is poorly understood. Thus, the biological role of autophagy in these diseases is still open to debate. During the last years, researchers have used a wide range of morphological, genetic and biochemical methods to monitor and manipulate the autophagic pathway and thus determine the specific role of this process in TSE. It has been suggested that PrPc could play a crucial role in modulating the autophagic pathway in neuronal cells, and the presence of abnormal autophagic activity has been frequently observed in several models of TSE both in vitro and in vivo, as well as in human prion diseases. Altogether, these findings suggest that autophagy is implicated in prion neuropathology and points to an impairment or failure of the process, potentially contributing to the pathogenesis of the disease. Additionally, autophagy is now emerging as a host defense response in controlling prion infection that plays a protective role by facilitating the clearance of aggregation-prone proteins accumulated within neurons. Since autophagy is one of the pathways of PrPSc degradation, and drug-induced stimulation of autophagic flux (the dynamic process of autophagic degradation activity) produces anti-prion effects, new treatments based on its activation have been tested to develop therapeutic strategies for prion diseases. In this review, we summarize previous and recent findings concerning the role of autophagy in TSE.
Idioma: Inglés
DOI: 10.3389/fbioe.2020.00975
Año: 2020
Publicado en: Frontiers in Bioengineering and Biotechnology 8 (2020), 975 [15 pp]
ISSN: 2296-4185

Factor impacto JCR: 5.89 (2020)
Categ. JCR: MULTIDISCIPLINARY SCIENCES rank: 12 / 73 = 0.164 (2020) - Q1 - T1
Factor impacto SCIMAGO: 1.081 - Bioengineering (Q1) - Histology (Q1) - Biotechnology (Q1) - Biomedical Engineering (Q1)

Financiación: info:eu-repo/grantAgreement/EUR/INTERREG-V-POCTEFA-2014-2020
Financiación: info:eu-repo/grantAgreement/ES/ISCIII/PI19-00144
Tipo y forma: Review (Published version)
Área (Departamento): Área Genética (Dpto. Anatom.,Embri.Genét.Ani.)
Área (Departamento): Área Sanidad Animal (Dpto. Patología Animal)


Creative Commons You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.


Exportado de SIDERAL (2022-02-08-11:24:57)


Este artículo se encuentra en las siguientes colecciones:
Articles



 Record created 2020-10-20, last modified 2022-02-08


Versión publicada:
 PDF
Rate this document:

Rate this document:
1
2
3
 
(Not yet reviewed)