Cell-to-cell Transmission of Polyglutamine Aggregates in C. elegans.
- Author:
Dong Kyu KIM
1
;
Kyu Won CHO
;
Woo Jung AHN
;
Dayana PEREZ-ACUÑA
;
Hyunsu JEONG
;
He Jin LEE
;
Seung Jae LEE
Author Information
- Publication Type:Original Article
- Keywords: Aging; Bimolecular Fluorescence Complementation; C. elegans; Huntington disease; Huntingtin; Protein aggregation
- MeSH: Age of Onset; Aging; Animals; Complement System Proteins; Disease Progression; Exons; Fluorescence; Glutamine; Humans; Huntington Disease; Inclusion Bodies; Mass Screening; Nerve Degeneration; Neurodegenerative Diseases; Neurons; Pharyngeal Muscles; Phenotype; Venus
- From:Experimental Neurobiology 2017;26(6):321-328
- CountryRepublic of Korea
- Language:English
- Abstract: Huntington disease (HD) is an inherited neurodegenerative disorder characterized by motor and cognitive dysfunction caused by expansion of polyglutamine (polyQ) repeat in exon 1 of huntingtin (HTT). In patients, the number of glutamine residues in polyQ tracts are over 35, and it is correlated with age of onset, severity, and disease progression. Expansion of polyQ increases the propensity for HTT protein aggregation, process known to be implicated in neurodegeneration. These pathological aggregates can be transmitted from neuron to another neuron, and this process may explain the pathological spreading of polyQ aggregates. Here, we developed an in vivo model for studying transmission of polyQ aggregates in a highly quantitative manner in real time. HTT exon 1 with expanded polyQ was fused with either N-terminal or C-terminal fragments of Venus fluorescence protein and expressed in pharyngeal muscles and associated neurons, respectively, of C. elegans. Transmission of polyQ proteins was detected using bimolecular fluorescence complementation (BiFC). Mutant polyQ (Q97) was transmitted much more efficiently than wild type polyQ (Q25) and forms numerous inclusion bodies as well. The transmission of Q97 was gradually increased with aging of animal. The animals with polyQ transmission exhibited degenerative phenotypes, such as nerve degeneration, impaired pharyngeal pumping behavior, and reduced life span. The C. elegans model presented here would be a useful in vivo model system for the study of polyQ aggregate propagation and might be applied to the screening of genetic and chemical modifiers of the propagation.
