White Thomas A, Kannan Mathur S, Walseth Timothy F
Department of Veterinary PathoBiology, College of Veterinary Medicine, University of Minnesota, St. Paul, USA.
FASEB J. 2003 Mar;17(3):482-4. doi: 10.1096/fj.02-0622fje. Epub 2003 Jan 22.
Cyclic ADP-ribose (cADPR) induces intracellular Ca2+ ([Ca2+]i) release in airway smooth muscle, and the cADPR antagonist, 8-amino-cADPR, abolishes [Ca2+]i oscillations elicited by acetylcholine (ACh), suggesting that cADPR is involved during muscarinic receptor activation. Whether the cADPR signaling pathway is common to agonists acting through different G protein-coupled receptors is not known. Using digital video imaging of Fura2-AM loaded porcine airway smooth muscle cells, we examined the effects of the membrane-permeant cADPR antagonist, 8-bromo-cADPR (8Br-cADPR), on the [Ca2+]i responses to ACh, histamine and endothelin-1 (ET-1). In cells preincubated with 100 microM 8Br-cADPR, the [Ca2+]i responses to ACh and ET-1 were significantly attenuated, whereas responses to histamine were not, suggesting agonist specificity of cADPR signaling. The effects of 8Br-cADPR were concentration dependent. We further examined whether muscarinic receptor subtypes specifically couple to this pathway, because in porcine airway smooth muscle cells, ACh activates both M2 and M3 muscarinic receptors coupled to Gai and Gaq, respectively. Methoctramine, an M2-selective antagonist, attenuated the [Ca2+]i responses to Ach, and there was no further attenuation by 8Br-cADPR. In airway smooth muscle, the CD38/cADPR signaling pathway is involved in [Ca2+]i responses to contractile agonists in an agonist-specific manner.
环磷酸腺苷核糖(cADPR)可诱导气道平滑肌细胞内钙离子([Ca2+]i)释放,而cADPR拮抗剂8-氨基-cADPR可消除乙酰胆碱(ACh)引发的[Ca2+]i振荡,这表明cADPR参与了毒蕈碱受体激活过程。目前尚不清楚cADPR信号通路是否为通过不同G蛋白偶联受体起作用的激动剂所共有。我们利用装载Fura2-AM的猪气道平滑肌细胞的数字视频成像技术,研究了膜通透性cADPR拮抗剂8-溴-cADPR(8Br-cADPR)对ACh、组胺和内皮素-1(ET-1)引起的[Ca2+]i反应的影响。在预先用100微摩尔8Br-cADPR孵育的细胞中,对ACh和ET-1的[Ca2+]i反应明显减弱,而对组胺的反应则未减弱,这表明cADPR信号具有激动剂特异性。8Br-cADPR的作用呈浓度依赖性。我们进一步研究了毒蕈碱受体亚型是否特异性地与该信号通路偶联,因为在猪气道平滑肌细胞中,ACh分别激活与Gai和Gaq偶联的M2和M3毒蕈碱受体。M2选择性拮抗剂甲溴东莨菪碱减弱了对ACh的[Ca2+]i反应,且8Br-cADPR没有进一步的减弱作用。在气道平滑肌中,CD38/cADPR信号通路以激动剂特异性方式参与对收缩性激动剂的[Ca2+]i反应。