Oleate Activates PLD2 Lipase and GEF Activity by Modulating Membrane Microdomain Dynamics via S-acylation

Guo, Zhiqiang; Bergeron, Karl-Frédérik et Mounier, Catherine (2025). « Oleate Activates PLD2 Lipase and GEF Activity by Modulating Membrane Microdomain Dynamics via S-acylation ». Prépublication. (Montréal, Québec, Canada, Univerisité du Québec à Montréal, Sciences biologiques). 40 p.

Fichier(s) associé(s) à ce document :
[img]
Prévisualisation
PDF (Article publié dans Journal of lipid Research)
Télécharger (24MB)

Résumé

Phospholipase D2 (PLD2) plays critical roles in cellular signaling, membrane dynamics, and cancer progression. Oleate (OA) has been shown to activate PLD2 and promote triple-negative breast cancer(TNBC) cell migration, but the underlying molecular mechanisms remain poorly understood. Using confocal microscopy, lipid raft isolation, and S-acylation assays, we show that OA enhanced PLD2 Sacylation at Cys223 and Cys224, disrupting its lipid raft localization, and consequently increasing its colocalization with PIP2-enriched microdomains. Furthermore, we identified PLD2 as a guanine nucleotide exchange factor (GEF) for Cdc42, with its GEF activity regulated by OA-dependent S-acylation and lipid raft dynamics. Mutation of the S-acylation sites or disruption of lipid rafts abolished PLD2-mediated Cdc42 activation and filopodia-like cell protrusion formation. These findings reveal a novel regulatory mechanism by which OA modulates PLD2 activity through S-acylation and membrane microdomain reorganization,providing new insights into the regulation of PLD2 in cell migration and signaling.

Type: Prépublication
Mots-clés ou Sujets: oleate, PLD2, S-acylation, Cdc42, lipid raft, guanine nucleotide exchange factor
Unité d'appartenance: Faculté des sciences > Département des sciences biologiques
Déposé par: Catherine Mounier
Date de dépôt: 03 déc. 2025 11:27
Dernière modification: 03 déc. 2025 11:27
Adresse URL : http://archipel.uqam.ca/id/eprint/19361

Statistiques

Voir les statistiques sur cinq ans...