Na+-K+-2Cl- cotransport in Ehrlich cells:: regulation by protein phosphatases and kinases

To identify protein kinases (PK) and phosphatases (PP) involved in regulation of the Na+-K+-2Cl(-) cotransporter in Ehrlich cells, the effect of various PK and PP inhibitors was examined. The PP-1, PP-2A, and PP-3 inhibitor calyculin A (Cal-A) was a potent activator of Na+-K+-2Cl(-) cotransport (EC50 = 35 nM). Activation by Cal-A was rapid (<1 min) but transient. Inactivation is probably due to a 10% cell swelling and/or the concurrent increase in intracellular Cl- concentration. Cell shrinkage also activates the Na+-K+-2Cl(-) cotransport system. Combining cell shrinkage with Gal-A treatment prolonged the cotransport activation compared with stimulation with Gal-A alone, suggesting PK stimulation by cell shrinkage. Shrinkage-induced cotransport activation was pH and Ca2+/calmodulin dependent. Inhibition of myosin light chain kinase by ML-7 and ML-9 or of PKA. by H-89 and KT-5720 inhibited cotransport activity induced by Gal-A and by cell shrinkage, with IC50 values similar to reported inhibition constants of the respective kinases in vitro. Cell shrinkage increased the ML-7-sensitive cotransport activity, whereas the H-89-sensitive activity was unchanged, suggesting that myosin light chain kinase is a modulator of the Na+-K+-2Cl(-) cotransport activity during regulatory volume increase.