Compartmentalized cAMP responses to prostaglandin EP₂ receptor activation in human airway smooth muscle cells

Previous studies indicate that prostaglandin EP₂ receptors selectively couple to AC2 in non-lipid raft domains of airway smooth muscle (ASM) cells, where they regulate specific cAMP-dependent responses. The goal of the present study was to identify the cellular microdomains where EP₂ receptors stimulate cAMP production.

FRET-based cAMP biosensors were targeted to different subcellular locations of primary human ASM cells. The Epac2-camps biosensor, which expresses throughout the cell, was used to measure bulk cytoplasmic responses. Epac2-MyrPalm and Epac2-CAAX were used to measure responses associated with lipid raft and non-raft regions of the plasma membrane respectively. Epac2-NLS was used to monitor responses at the nucleus.

Activation of AC with forskolin or β₂ -adrenoceptors with isoprenaline increased cAMP in all subcellular locations. Activation of EP₂ receptors with butaprost produced cAMP responses that were most readily detected by the non-raft and nuclear sensors, but only weakly detected by the cytosolic sensor and not detected at all by the lipid raft sensor. Exposure to rolipram, a PDE4 inhibitor, unmasked the ability of EP₂ receptors to increase cAMP levels associated with lipid raft domains. Overexpression of AC2 selectively increased EP₂ receptor-stimulated production of cAMP in non-raft membrane domains.

EP₂ receptor activation of AC2 leads to cAMP production in non-raft and nuclear compartments of human ASMs, while β₂ adrenoceptor signalling is broadly detected across microdomains. The activity of PDE4 appears to play a role in maintaining the integrity of compartmentalized EP₂ receptor responses in these cells.