P2-purinergic stimulation of iodide efflux in FRTL-5 rat thyroid cells involves parallel activation of PLC and PLA2.

Abstract

Extracellular ATP increases inositol phosphates, cytosolic Ca2+ concentration ([Ca2+]i), arachidonic acid (AA) release, and iodide efflux in FRTL-5 cells. To examine the sequence of events in P2-purinergic receptor activation by ATP, a phospholipase C (PLC) inhibitor (U-73122) and a phospholipase A2 (PLA2) inhibitor (U-26384), as well as 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'- tetraacetic acid (BAPTA) and downregulation of protein kinase C (PKC) were used. ATP increased inositol trisphosphate (IP3), [Ca2+]i, AA release, and 125I efflux dose dependently. U-73122 inhibited the IP3 and calcium increase but not AA; U-26384 prevented AA release but not the increase in calcium. Both agents inhibited iodide efflux. BAPTA prevented any ATP-induced increase in [Ca2+]i without affecting AA release or 125I efflux. PKC downregulation had no effect on ATP-stimulated AA release, but reduced 125I efflux. We conclude that ATP-induced iodide efflux involves parallel, not sequential, activation of PLC and PLA2. No increase in [Ca2+]i or PKC activity is required for PLA2 activation. In contrast, an increase in 125I efflux depends on PKC and PLA2 activities, but not an increase in [Ca2+]i.