Cyclic ADP-ribose, a putative Ca2+-mobilizing second messenger, operates in submucosal gland acinar cells

Abstract

Cyclic ADP-ribose (cADPR), a putative Ca2+-mobilizing second messenger, has been reported to operate in several mammalian cells. To investigate whether cADPR is involved in electrolyte secretion from airway glands, we used a patch-clamp technique, the measurement of microsomal Ca2+release, quantification of cellular cADPR, and RT-PCR for CD38 mRNA in human and feline tracheal glands. cADPR (>6 μM), infused into the cell via the patch pipette, caused ionic currents dependent on cellular Ca2+. Infusions of lower concentrations (2–4 μM) of cADPR or inositol 1,4,5-trisphosphate (IP3) alone were without effect on the baseline current, but a combined application of cADPR and IP3mimicked the cellular response to low concentrations of acetylcholine (ACh). Microsomes derived from the isolated glands released Ca2+in response to both IP3and cADPR. cADPR released Ca2+from microsomes desensitized to IP3or those treated with heparin. The mRNA for CD38, an enzyme protein involved in cADPR metabolism, was detected in human tissues, including tracheal glands, and the cellular content of cADPR was increased with physiologically relevant concentrations of ACh. We conclude that cADPR, in concert with IP3, operates in airway gland acinar cells to mobilize Ca2+, resulting in Cl−secretion.