<scp>ALOX15</scp> links lipid metabolism to receptor trafficking in platelet activation
Platelet activation is traditionally viewed as a signaling process initiated by receptor engagement. In this issue of The FEBS Journal, Govatati et al. identify an additional regulatory layer linking lipid metabolism to receptor trafficking. The authors show that ALOX15-derived lipid mediators promote PKCθ-NMT1-dependent myristoylation of PAR4, thereby facilitating its membrane localization and platelet activation. These findings position receptor lipidation and trafficking as active regulatory mechanisms in platelet activation and suggest new opportunities for therapeutic modulation of hemostasis.
Authors
- Sharad Saxena (ORCID: https://orcid.org/0000-0002-9379-4940)
- Serena Zacchigna (ORCID: https://orcid.org/0000-0001-6705-3076)
- Yosef Eshetie Amare (ORCID: https://orcid.org/0000-0003-0030-9529)
Institutions
- University of Trieste (IT)
- University of Nova Gorica (SI)
- School Centre Nova Gorica (SI)
- International Centre for Genetic Engineering and Biotechnology (IT)
Publication Details
- Journal
- FEBS Journal
- Published
- 2026-06-29
- DOI
- https://doi.org/10.1111/febs.70637
- Primary Topic
- Platelet Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00