An Experimental Model of Neurodegenerative Disease Based on Porcine Hemagglutinating Encephalomyelitis Virus-Related Lysosomal Abnormalities

Mol Neurobiol. 2020 Dec;57(12):5299-5306. doi: 10.1007/s12035-020-02105-y. Epub 2020 Sep 2.

Abstract

Lysosomes are involved in pathogenesis of a variety of neurodegenerative diseases and play a large role in neurodegenerative disorders caused by virus infection. However, whether virus-infected cells or animals can be used as experimental models of neurodegeneration in humans based on virus-related lysosomal dysfunction remain unclear. Porcine hemagglutinating encephalomyelitis virus displays neurotropism in mice, and neural cells are its targets for viral progression. PHEV infection was confirmed to be a risk factor for neurodegenerative diseases in the present. The findings demonstrated for the first time that PHEV infection can lead to lysosome disorders and showed that the specific mechanism of lysosome dysfunction is related to PGRN expression deficiency and indicated similar pathogenesis compared with human neurodegenerative diseases upon PHEV infection. Trehalose can also increase progranulin expression and rescue abnormalities in lysosomal structure in PHEV-infected cells. In conclusion, these results suggest that PHEV probably serve as a disease model for studying the pathogenic mechanisms and prevention of other degenerative diseases.

Keywords: Lysosomal abnormalities; Neurodegenerative diseases; Porcine hemagglutinating encephalomyelitis virus; Progranulin; Trehalose.

MeSH terms

  • Animals
  • Betacoronavirus 1 / physiology*
  • Cell Line, Tumor
  • Coronavirus Infections / pathology
  • Coronavirus Infections / virology
  • DNA-Binding Proteins / metabolism
  • Disease Models, Animal
  • Lysosomes / drug effects
  • Lysosomes / pathology*
  • Male
  • Mice, Inbred BALB C
  • Neurodegenerative Diseases / pathology*
  • Neurodegenerative Diseases / virology*
  • Progranulins / metabolism
  • Swine
  • Trehalose / pharmacology

Substances

  • DNA-Binding Proteins
  • Progranulins
  • TDP-43 protein, mouse
  • Trehalose