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Kinting, S.* ; Li, Y.* ; Forstner, M.* ; Delhommel, F. ; Sattler, M. ; Griese, M.*

Potentiation of ABCA3 lipid transport function by ivacaftor and genistein.

J. Cell. Mol. Med. 23, 5225-5234 (2019)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
ABCA3 is a phospholipid transporter implicated in pulmonary surfactant homoeostasis and localized at the limiting membrane of lamellar bodies, the storage compartment for surfactant in alveolar type II cells. Mutations in ABCA3 display a common genetic cause for diseases caused by surfactant deficiency like respiratory distress in neonates and interstitial lung disease in children and adults, for which currently no causal therapy exists. In this study, we investigated the effects of ivacaftor and genistein, two potentiators of the cystic fibrosis transmembrane conductance regulator (CFTR), on ABCA3-specific lipid transport function. Wild-type (WT) and functional ABCA3 mutations N568D, F629L, G667R, T1114M and L1580P were stably expressed in A549 cells. Three-dimensional modelling predicted functional impairment for all five mutants that was confirmed by in vitro experiments (all <14% of WT functional activity). Treatment with potentiators rescued the mutants N568D (up to 114% of WT), F629L (up to 47% of WT), and G667R (up to 60% of WT), the latter variation needing higher concentrations of genistein, showing reduced affinity of the potentiator to the mutant protein. Our results present a first proof that functional ABCA3 mutations are rescued by CFTR potentiators, making them a potential therapeutical option for patients suffering from surfactant deficiency due to ABCA3 mutations.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Abca3 ; Cftr Potentiators ; Genistein ; Interstitial Lung Disease ; Ivacaftor; Transmembrane-conductance-regulator; Cystic-fibrosis; Pulmonary Surfactant; Intracellular Vesicles; Membrane-protein; Binding-sites; In-vitro; Cftr Cl; Mutations; Mutants
ISSN (print) / ISBN 1582-1838
e-ISSN 1582-4934
Zeitschrift Journal of Cellular and Molecular Medicine
Quellenangaben Band: 23, Heft: 8, Seiten: 5225-5234 Artikelnummer: , Supplement: ,
Verlag Blackwell
Verlagsort 111 River St, Hoboken 07030-5774, Nj Usa
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Structural Biology (STB)