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Published ahead of print on June 10, 2004, doi:10.1165/rcmb.2004-0035OC

Am. J. Respir. Cell Mol. Biol., Volume 31, Number 3, September 2004, 302-308

A more recent version of this article appeared on September 1, 2004
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Submitted on February 4, 2004
Revised on June 9, 2004

Expression and functions of the duodenal peptide secretin and its receptor in human lung

Richard J Davis1*, Keith J Page1, Gabriela J Dos Santos Cruz1, Dan W Harmer1, Peter W Munday2, Sandra J Williams1, Joanna Picot3, Tom J Evans4, Robert L Sheldrick1, Robert A Coleman1, and Kenneth L Clark1

1 Exploratory Target Profiling, Pharmagene Laboratories, Royston, Hertfordshire, United Kingdom, 2 Exploratory Target Profiling, Pharmagene Laboratories, Royston, Hertfordshire, United Kingdom; Inpharmatica, London, United Kingdom, 3 Department of Infectious Disease, Imperial College, London, United Kingdom, 4 Department of Infectious Disease, Imperial College, London, United Kingdom; Division of Immunology, Infection and Inflammation, University of Glasgow, Glasgow, United Kingdom

* To whom correspondence should be addressed. E-mail: richard.davis{at}pharmagene.com.

The physiological role of the duodenal peptide secretin is as a potent stimulant of electrolyte and water movement in pancreatic and biliary epithelium, via activation of G-protein coupled secretin receptors (hSCTR). However, the distribution and potential function of hSCTR in human lung has not previously been addressed. Using real-time quantitative reverse transcriptase-polymerase chain reaction profiling, in situ hybridisation and immunohistochemistry, we demonstrated that the hSCTR is abundantly expressed within the distal regions of human lung (tertiary bronchus and parenchyma), with negligible expression detected in more proximal regions (trachea, primary and secondary bronchus). Expression was observed predominantly on the basolateral membrane of the bronchial epithelial layer with some expression also observed in bronchial smooth muscle. In primary cultures of human tertiary bronchial epithelial cells, secretin was demonstrated to potently stimulate channel mediated Cl- efflux in a concentration-dependent manner. Secretin was also shown to cause concentration-dependent relaxation of human tertiary bronchial smooth muscle. In summary, these data demonstrate that secretin receptors are present in human lung, and that activation of these receptors with human secretin potently stimulates concentration-dependent Cl- efflux from bronchial epithelial cells and bronchorelaxation.







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