• Michele Ettorre, Genny Verzè, Sara Caldrer, Jan Johansson, Elisa Calcaterra, Baroukh Maurice Assael, Paola Melotti, Claudio Sorio, and Mario Buffelli.
• Department of Neurological and Movement Sciences, Section of Physiology, University of Verona, Strada Le Grazie 8, 37134 Verona, Italy; Center for Biomedical Computing, University of Verona, Strada le Grazie 8, 37134 Verona, Italy. Electronic address: michele.ettorre@gmail.com.
• Biochim. Biophys. Acta. 2014 Oct 1; 1840 (10): 3088-95.

BackgroundCystic fibrosis is caused by mutations of CFTR gene, a protein kinase A-activated anion channel, and is associated to a persistent and excessive chronic lung inflammation, suggesting functional alterations of immune cells. Leukocytes express detectable levels of CFTR but the molecule has not been fully characterized in these cells.MethodsFreshly isolated monocytes from healthy individuals and CF patients were assessed by protein expression, single cell electrophysiological and membrane depolarization assays.ResultsWe recorded chloride currents by patch clamp in healthy monocytes, after the administration of a CFTR stimulus. Currents were sensitive to a specific blocker of the CFTR channel, CFTRinh-172 and were absent in CF monocytes. Next, we evaluated the effects of ex vivo exposure of monocytes from cystic fibrosis patients carrying the F508del mutation to a chemical corrector, Vertex-325. We found an increase in CFTR expression by confocal microscopy and a recovery of CFTR function by both patch clamp and single cell fluorescence analysis.ConclusionsWe confirm the expression of functional CFTR in human monocytes and demonstrate that blood monocytes can represent an adequate source of primary cells to assess new therapies and define diagnosis of CF.General SignificanceTests to evaluate CFTR functional abnormalities in CF disease might greatly benefit from the availability of a convenient source of primary cells. This electrophysiological study promotes the use of monocytes as a minimally invasive tool to study and monitor CFTR function in individual patients.Copyright © 2014 Elsevier B.V. All rights reserved.

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