A Single Amino Acid Substitution, Found in Mammals with Low Susceptibility to Prion Diseases, Delays Propagation of Two Prion Strains in Highly Susceptible Transgenic Mouse Models

Otero, A. ; Hedman, C. ; Fernández-Borges, N. ; Eraña, H. ; Marín, B. (Universidad de Zaragoza) ; Monzón, M. (Universidad de Zaragoza) ; Sánchez-Martín, M.A. ; Nonno, R. ; Badiola, J.J. (Universidad de Zaragoza) ; Bolea, R. (Universidad de Zaragoza) ; Castilla, J.

Resumen: Specific variations in the amino acid sequence of prion protein (PrP) are key determinants of susceptibility to prion diseases. We previously showed that an amino acid substitution specific to canids confers resistance to prion diseases when expressed in mice and demonstrated its dominant-negative protective effect against a variety of infectious prion strains of different origins and characteristics. Here, we show that expression of this single amino acid change significantly increases survival time in transgenic mice expressing bank vole cellular prion protein (PrP C ), which is inherently prone to misfolding, following inoculation with two distinct prion strains (the CWD-vole strain and an atypical strain of spontaneous origin). This amino acid substitution hinders the propagation of both prion strains, even when expressed in the context of a PrP C uniquely susceptible to a wide range of prion isolates. Non-inoculated mice expressing this substitution experience spontaneous prion formation, but showing an increase in survival time comparable to that observed in mutant mice inoculated with the atypical strain. Our results underscore the importance of this PrP variant in the search for molecules with therapeutic potential against prion diseases.

Idioma: Inglés

DOI: 10.1007/s12035-019-1535-0

Año: 2019

Publicado en: MOLECULAR NEUROBIOLOGY (2019), 1-11
ISSN: 0893-7648

Factor impacto JCR: 4.5 (2019)

Categ. JCR: NEUROSCIENCES rank: 65 / 271 = 0.24 (2019) - Q1 - T1

Factor impacto SCIMAGO: 1.482 - Neurology (Q1) - Neuroscience (miscellaneous) (Q1) - Cellular and Molecular Neuroscience (Q2)

Financiación: info:eu-repo/grantAgreement/ES/DGA/C020-2014
Financiación: info:eu-repo/grantAgreement/EUR/INTERREG-POCTEFA/EFA-148-16 REDPRION
Financiación: info:eu-repo/grantAgreement/ES/MINECO-FEDER/AGL2015-65046-C2-1-R
Financiación: info:eu-repo/grantAgreement/ES/MINECO-FEDER/AGL2015-65560-R

Tipo y forma: Artículo (PostPrint)

Área (Departamento): Área Sanidad Animal (Dpto. Patología Animal)
Área (Departamento): Area Histología (Dpto. Anatom.Histolog.Humanas)