Regulation of transepithelial ion transport and intracellular calcium by extracellular ATP in human normal and cystic fibrosis airway epithelium

SJ Mason, AM Paradiso… - British journal of …, 1991 - Wiley Online Library
SJ Mason, AM Paradiso, RC Boucher
British journal of pharmacology, 1991Wiley Online Library
1 The role of extracellular nucleotides in regulation of ion transport activities (short circuit
current, Isc) of human respiratory epithelia was studied. 2 Application of nucleotides to the
apical or basolateral membrane of human nasal epithelium induced a concentration‐
dependent increase in Isc. 3 The rank order of potency of purine‐or pyrimidine‐induced
changes in Isc of normal human nasal epithelium when applied to the apical membrane
(UTP≥ ATP> ATPγS> 2MeSATP> ADPβS≫ βγMeATP≥ βγMeATP) or basolateral …
  • 1
    The role of extracellular nucleotides in regulation of ion transport activities (short circuit current, Isc) of human respiratory epithelia was studied.
  • 2
    Application of nucleotides to the apical or basolateral membrane of human nasal epithelium induced a concentration‐dependent increase in Isc.
  • 3
    The rank order of potency of purine‐ or pyrimidine‐induced changes in Isc of normal human nasal epithelium when applied to the apical membrane (UTP ≥ ATP > ATPγS > 2MeSATP > ADPβS ≫ βγMeATP ≥ βγMeATP) or basolateral membrane (2MeSATP > UTP > ATP > ATPγS > αβMeATP > βγMeATP) is consistent with involvement of a P2 purinoceptor. A similar rank order of potencies was observed for nucleotide effects on intracellular calcium measured by Fura‐2 fluorescence using microspectrofluorimetry.
  • 4
    Similar nucleotide potency in the regulation of ion transport and intracellular calcium in cystic fibrosis (CF) airway epithelium (UTP ≥ ATP) was observed, suggesting purinoceptors might be used to stimulate ion transport processes that would promote hydration of airway secretions and facilitate their clearance from CF lungs.
  • 5
    These data provide evidence for the regulation of ion transport by P2 purinoceptors in normal and cystic fibrosis human airway epithelium.
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