Molecular Pathophysiological Mechanisms in Huntington's Disease

Huntington's disease is an inherited neurodegenerative disease described 150 years ago by George Huntington. The genetic defect was identified in 1993 to be an expanded CAG repeat on exon 1 of the huntingtin gene located on chromosome 4. In the following almost 30 years, a considerable amount of research, using mainly animal models or in vitro experiments, has tried to unravel the complex molecular cascades through which the transcription of the mutant protein leads to neuronal loss, especially in the medium spiny neurons of the striatum, and identified excitotoxicity, transcriptional dysregulation, mitochondrial dysfunction, oxidative stress, impaired proteostasis, altered axonal trafficking and reduced availability of trophic factors to be crucial contributors. This review discusses the pathogenic cascades described in the literature through which mutant huntingtin leads to neuronal demise. However, due to the ubiquitous presence of huntingtin, astrocytes are also dysfunctional, and neuroinflammation may additionally contribute to Huntington's disease pathology. The quest for therapies to delay the onset and reduce the rate of Huntington's disease progression is ongoing, but is based on findings from basic research.

Automated summary

Huntington's disease is an inherited neurodegenerative disease that primarily affects medium spiny neurons in the striatum. The mutant huntingtin protein leads to neuronal loss through a series of molecular cascades, involving excitotoxicity, transcriptional dysregulation, and other key factors. In addition to neurons, astrocytes are also dysfunctional due to the presence of mutant huntingtin, and neuroinflammation may further contribute to the pathogenesis of Huntington's disease.