Huntingtin and its allies at the cortico-striatal synapse
Huntington's Disease (HD) is characterized by progressive motor and cognitive decline, largely driven by cortico-striatal synaptic dysfunction. Central to these processes is huntingtin (HTT) protein, which is abundantly present at the synapse. HTT regulates the synaptic vesicle cycle at presynaptic terminals and serves as a scaffold at the postsynaptic density where it modulates receptor dynamics. An expanding network of HTT-interacting proteins (HIPs), crucial for maintaining synaptic structure and function, underscores the role of HTT as a core component of synaptic integrity. This review examines the 30-year research journey that has unveiled HTT pre- and postsynaptic partners, with focus on experimentally validated interactors and their involvement in HD cortico-striatal synaptic dysfunction.
Authors
- Raffaele Iennaco (ORCID: https://orcid.org/0000-0002-7309-7232)
- Chiara Zuccato (ORCID: https://orcid.org/0000-0003-1771-3392)
- Andrea Scolz (ORCID: https://orcid.org/0009-0005-6227-7608)
Institutions
- University of Milan (IT)
- Istituto Nazionale Genetica Molecolare (IT)
Publication Details
- Journal
- Cell Death and Disease
- Published
- 2026-03-27
- DOI
- https://doi.org/10.1038/s41419-026-08584-6
- Primary Topic
- Genetic Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00