cAMP and Ca2+ act co-operatively on the Cl- conductance of HT29 cells.

Previous studies in HT29 cells have revealed that the Cl- channels induced by cAMP or by increasing cytosolic Ca2+, e.g. by addition of ATP, and by hypotonic cell swelling share in common all examined properties, such as ion selectivity and blocker sensitivity. In addition, it was shown that conductances induced by either pathway were not additive. Therefore all three pathways apparently act on the same type of small conductance Cl- channel. In CFPAC-1 cells the general properties of the Cl- conductance were identical. However, the cAMP response was absent. In both cell types the Ca(2+)-mediated conductance response was transient. Here we examine the kinetics of the conductance increases induced by neurotensin (NT, 10(-8) mol/l) or ATP (10(-5) mol/l) in HT29 and CFPAC-1 cells using the slow (nystatin) or fast whole cell patch clamp technique, and we ask whether cAMP influences these kinetics. In the continuous presence of NT the conductance response in both cell types was very transient. It collapsed with a time constant (tau) of 39 (30-56 s) in HT29 and of 33 (27-41 s) in CFPAC-1 cells. The ATP response was also transient with a tau of 49 (42-57 s) in HT29 cells and 102 (77-152 s) in CFPAC-1 cells. Pre-treatment by membrane permeable cAMP (10(-3) mol/l) enhanced the baseline conductance in HT29 but not in CFPAC-1 cells. Furthermore, the ATP- and NT-induced conductance increases became significantly less transient in HT29 but not in CFPAC-1 cells.(ABSTRACT TRUNCATED AT 250 WORDS)