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Expression of P2Y receptors in cell lines derived from the human lung
Author(s) -
Communi Didier,
Paindavoine Pascale,
Place Graham A,
Parmentier Marc,
Boeynaems JeanMarie
Publication year - 1999
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0702560
Subject(s) - p2y receptor , cell culture , receptor , biology , microbiology and biotechnology , a549 cell , cell , purinergic receptor , biochemistry , genetics
Northern blotting experiments have been performed with RNA extracted from several cell lines derived from the human lung in order to detect P2Y 1 , P2Y 2 , P2Y 4 and P2Y 6 mRNA. We have investigated the 1HAEo− and 16HBE14o− epithelial cell lines derived from the airway epithelium, the A549 cell line displaying properties of type II alveolar epithelial cells, the CALU‐3 serous cells, the 6CFSMEo− submucosal cells and the HASMSC1 airway smooth muscle cells. We have also evaluated one pancreatic epithelial cell line called CFPAC‐1. These experiments revealed that P2Y 2 and P2Y 6 mRNA are co‐expressed in the 1HAEo−, 16HBE14o− and A549 epithelial cell lines. The CFPAC‐1 pancreatic cell line was strongly positive for the P2Y 2 receptor. No signal was obtained for the P2Y 1 and P2Y 4 receptors. We have then performed RT–PCR experiments with specific oligonucleotides of these last two P2Y receptors with the RNA used for the Northern blotting experiments. P2Y 4 mRNA was detected in five cell lines: 1HAEo−, 16HBE14o−, 6CFSMEo−, HASMSC1 and CFPAC‐1. P2Y 1 mRNA was only detected in the CALU‐3 cell line. Inositol trisphosphates assays have identified a response typical of the P2Y 2 receptor in the 1HAEo− and the 16HBE14o− airway epithelial cell lines which co‐express P2Y 2 and P2Y 6 mRNA. By contrast, the 6CFSMEo− submucosal cells expressed a UTP‐specific response which displayed pharmacological characteristics compatible with the human P2Y 4 receptor: in particular, there was no response to UDP or ATP and the UTP effect was totally inhibited by pertussis toxin.British Journal of Pharmacology (1999) 127 , 562–568; doi: 10.1038/sj.bjp.0702560