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How COVID-19 Hijacks the Cytoskeleton: Therapeutic Implications
Maral Aminpour1, Stuart Hameroff2,3,4, Jack A Tuszynski5,6
1Department of Biomedical Engineering, University of Alberta, Edmonton, AB T6G 1Z2, Canada.
The SARS-CoV-2 virus hijacks host cell microtubules for replication and spread, causing COVID-19 pathology. Targeting host microtubules and the microtubule-organizing center offers a novel therapeutic strategy.
Area of Science:
- Cell Biology
- Virology
- Immunology
Background:
- SARS-CoV-2 infection disrupts host cell functions by co-opting the microtubule cytoskeleton.
- Viral hijacking of microtubules facilitates intracellular trafficking, cell-to-cell spread, and immune dysfunction.
Purpose of the Study:
- To investigate the mechanism by which SARS-CoV-2 interacts with the host cell's microtubule-organizing center.
- To propose novel therapeutic strategies targeting host cell components crucial for viral replication.
Main Methods:
- Analysis of viral-host cell interactions at the molecular level, focusing on the microtubule cytoskeleton.
- Exploration of potential therapeutic interventions targeting microtubules and the microtubule-organizing center.
Main Results:
- SARS-CoV-2 may dock within the microtubule-organizing center's centrioles, utilizing interactions between viral spike proteins and microtubule C-termini.
- This interaction enables viral replication, cell spread, and immune dysregulation.
Conclusions:
- Therapies targeting host cell microtubules and the microtubule-organizing center are a promising alternative for COVID-19 treatment.
- Potential therapies include anti-microtubule drugs or low-intensity ultrasound applied to the vagus nerve or spleen.
Related Concept Videos
Intracellular Movement of Viruses and Bacteria
Adaptability of Cytoskeletal Filaments
Studying the Cytoskeleton
Destabilization of Microtubules
Assembly of Cytoskeletal Filaments
Cytoskeletal Coordination in Cell Migration

