Abstract
The importance of impaired HCO3 secretion in the pathophysiology of the pancreas of cystic fibrosis (CF) patients has been well documented and known for many years (1). Studies in 1990s from the Welsh (2) and Boucher (3) laboratories suggested that HCO3 secretion may also be impaired in the airways of CF patients. Perhaps because Cl- secretion has been assumed to be of higher importance and thus received the greater attention, the transcellular mechanisms of HCO3 secretion remain poorly understood and underinvestigated. Studies from our own laboratory (4) and the laboratories of Wine and Widdicombe (5) have now established that the human airway serous cell line, Calu-3 cells, secrete HCO3 and not Cl-, in response to a cAMP-mediated secretory agonist. Serous cells are the most abundant cell type of the submucosal glands (6) and are the predominate site of CFTR expression in the airways (7,8). Thus, a better understanding of the transport mechanisms of serous cells is of critical importance in establishing how mutations in CFTR lead to submucosal gland and airways pathophysiology. The focus of this chapter is to provide a description of the methods used to study Calu-3 cell monolayers grown on permeable supports by the short-circuit current (ISC) technique. In addition, methods for ion flux studies and ion substitution studies of short-circuited monolayers are described along with background information necessary to interpret the experimental results specifically as they relate to the net secretion of HCO3 . To introduce the subject of HCO3 secretion, we provide a brief description of the mechanisms of transepithelial HCO3 secretion as they are presently understood.
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Bridges, R.J. (2002). Transepithelial Measurements of Bicarbonate Secretion in Calu-3 Cells. In: Skach, W.R. (eds) Cystic Fibrosis Methods and Protocols. Methods in Molecular Medicine™, vol 70. Humana Press. https://doi.org/10.1385/1-59259-187-6:111
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DOI: https://doi.org/10.1385/1-59259-187-6:111
Publisher Name: Humana Press
Print ISBN: 978-0-89603-897-4
Online ISBN: 978-1-59259-187-9
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