SERCA and PMCA pumps contribute to the deregulation of Ca(2+) homeostasis in human CF epithelial cells. - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Biochimica et Biophysica Acta - Molecular Cell Research Année : 2015

SERCA and PMCA pumps contribute to the deregulation of Ca(2+) homeostasis in human CF epithelial cells.

Résumé

Cystic Fibrosis (CF) disease is caused by mutations in the CFTR gene (CF transmembrane conductance regulator). F508 deletion is the most represented mutation, and F508del-CFTR is absent of plasma membrane and accumulates into the endoplasmic reticulum (ER) compartment. Using specific Ca2+ genetics cameleon probes, we showed in the human bronchial CF epithelial cell line CFBE that ER Ca2+ concentration was strongly increased compared to non-CF (16HBE) cells, and normalized by the F508del-CFTR corrector agent, VX-809. We also showed that ER F508del-CFTR retention increases SERCA (Sarcoplasmic/Reticulum Ca2+ ATPase) pump activity whereas PMCA (Plasma Membrane Ca2+ ATPase) activities were reduced in these CF cells compared to corrected CF cells (VX-809) and non-CF cells. We are showing for the first time CFTR/SERCA and CFTR/PMCA interactions that are modulated in CF cells and could explain part of Ca2+ homeostasis deregulation due to mislocalization of F508del-CFTR. Using ER or mitochondria genetics Ca2+ probes, we are showing that ER Ca2+ content, mitochondrial Ca2+ uptake, SERCA and PMCA pump, activities are strongly affected by the localization of F508del-CFTR protein.

Dates et versions

hal-01134260 , version 1 (23-03-2015)

Identifiants

Citer

Réginald Philippe, Fabrice Antigny, Paul Buscaglia, Caroline Norez, Frédéric Becq, et al.. SERCA and PMCA pumps contribute to the deregulation of Ca(2+) homeostasis in human CF epithelial cells.. Biochimica et Biophysica Acta - Molecular Cell Research, 2015, 1853 (5), pp.892-903. ⟨10.1016/j.bbamcr.2015.01.010⟩. ⟨hal-01134260⟩
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