Spatio-temporal propagation of [Ca.sup.2+] signals by cyclic ADP-ribose in 3T3 cells stimulated via purinergic P2Y receptors

The role of cyclic ADP-ribose in the amplification of subcellular and global [Ca.sup.2+] signaling upon stimulation of P2Y purinergic receptors was studied in 3T3 fibroblasts. Either (1) 3T3 fibroblasts (CD3[8.sup.-] cells), (2) 3T3 fibroblasts preloaded by incubation with extracellular cyclic ADP-ribose (cADPR), (3) 3T3 fibroblasts microinjected with ryanodine, or (4) 3T3 fibroblasts transfected to express the ADP-ribosyl cyclase CD38 (CD3[8.sup.+] cells) were used. Both preincubation with cADPR and CD38 expression resulted in comparable intracellular amounts of cyclic ADP-ribose (42.3 [+ or -] 5.2 and 50.5 [+ or -] 8.0 pmol/mg protein). P2Y receptor stimulation of CD38- cells yielded a small increase of intracellular [Ca.sup.2+] concentration and a much higher [Ca.sup.2+] signal in CD38-transfected cells, in cADPR-preloaded cells, or in cells microinjected with ryanodine. Confocal [Ca.sup.2+] imaging revealed that stimulation of ryanodine receptors by cADPR or ryanodine amplified localized pacemaker [Ca.sup.2+] signals with properties resembling [Ca.sup.2+] quarks and triggered the propagation of such localized signals from the plasma membrane toward the internal environment, thereby initiating a global [Ca.sup.2+] wave.