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1.
Brain ; 144(9): 2745-2758, 2021 10 22.
Artigo em Inglês | MEDLINE | ID: mdl-34687213

RESUMO

Human prion diseases are fatal neurodegenerative disorders that include sporadic, infectious and genetic forms. Inherited Creutzfeldt-Jakob disease due to the E200K mutation of the prion protein-coding gene is the most common form of genetic prion disease. The phenotype resembles that of sporadic Creutzfeldt-Jakob disease at both the clinical and pathological levels, with a median disease duration of 4 months. To date, there is no available treatment for delaying the occurrence or slowing the progression of human prion diseases. Existing in vivo models do not allow high-throughput approaches that may facilitate the discovery of compounds targeting pathological assemblies of human prion protein or their effects on neuronal survival. Here, we generated a genetic model in the nematode Caenorhabditis elegans, which is devoid of any homologue of the prion protein, by expressing human prion protein with the E200K mutation in the mechanosensitive neuronal system. Expression of E200K prion protein induced a specific behavioural pattern and neurodegeneration of green fluorescent protein-expressing mechanosensitive neurons, in addition to the formation of intraneuronal inclusions associated with the accumulation of a protease-resistant form of the prion protein. We demonstrated that this experimental system is a powerful tool for investigating the efficacy of anti-prion compounds on both prion-induced neurodegeneration and prion protein misfolding, as well as in the context of human prion protein. Within a library of 320 compounds that have been approved for human use and cross the blood-brain barrier, we identified five molecules that were active against the aggregation of the E200K prion protein and the neurodegeneration it induced in transgenic animals. This model breaks a technological limitation in prion therapeutic research and provides a key tool to study the deleterious effects of misfolded prion protein in a well-described neuronal system.


Assuntos
Proteínas de Caenorhabditis elegans/genética , Modelos Animais de Doenças , Doenças Priônicas/genética , Proteínas Priônicas/genética , Tubulina (Proteína)/genética , Animais , Animais Geneticamente Modificados , Benzocaína/administração & dosagem , Benzocaína/análogos & derivados , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Encéfalo/patologia , Caenorhabditis elegans , Humanos , Naloxona/administração & dosagem , Piroxicam/administração & dosagem , Piroxicam/análogos & derivados , Doenças Priônicas/tratamento farmacológico , Doenças Priônicas/metabolismo , Proteínas Priônicas/metabolismo , Agregação Patológica de Proteínas/tratamento farmacológico , Agregação Patológica de Proteínas/genética , Agregação Patológica de Proteínas/metabolismo
2.
J Infect Dis ; 209(7): 1144-8, 2014 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-24265435

RESUMO

In prion diseases, a major issue in therapeutic research is the variability of the effect between strains. Stimulated by the report of an antiprion effect in a scrapie model and by ongoing international clinical trials using doxycycline, we studied the efficacy of cyclines against the propagation of human prions. First, we successfully propagated various Creutzfeldt-Jakob disease (CJD) isolates (sporadic, variant, and iatrogenic CJD) in neuronal cultures expressing the human prion protein. Then, we found that doxycycline was the most effective compound, with important variations between isolates. Isolates from sporadic CJD, the most common form of prion disease, showed the highest sensitivity.


Assuntos
Doxiciclina/farmacologia , Neurônios/efeitos dos fármacos , Neurônios/metabolismo , Príons/antagonistas & inibidores , Príons/efeitos dos fármacos , Células Cultivadas , Doxiciclina/metabolismo , Doxiciclina/uso terapêutico , Humanos
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