Frings S
Department of Physiology, Universität des Saarlandes, Homburg/Saar, Germany.
J Gen Physiol. 1993 Feb;101(2):183-205. doi: 10.1085/jgp.101.2.183.
Effects of neurotransmitters on cAMP-mediated signal transduction in frog olfactory receptor cells (ORCs) were studied using in situ spike recordings and radioimmunoassays. Carbachol, applied to the mucosal side of olfactory epithelium, amplified the electrical response of ORCs to cAMP-generating odorants, but did not affect unstimulated cells. A similar augmentation of odorant response was observed in the presence of phorbol dibutyrate (PDBu), an activator of protein kinase C (PKC). The electrical response to forskolin, an activator of adenylate cyclase (AC), was also enhanced by PDBu, and it was attenuated by the PKC inhibitor Goe 6983. Forskolin-induced accumulation of cAMP in olfactory tissue was potentiated by carbachol, serotonin, and PDBu to a similar extent. Potentiation was completely suppressed by the PKC inhibitors Goe 6983, staurosporine, and polymyxin B, suggesting that the sensitivity of olfactory AC to stimulation by odorants and forskolin was increased by PKC. Experiments with deciliated olfactory tissue indicated that sensitization of AC was restricted to sensory cilia of ORCs. To study the effects of cell Ca2+ on these mechanisms, the intracellular Ca2+ concentration of olfactory tissue was either increased by ionomycin or decreased by BAPTA/AM. Increasing cell Ca2+ had two effects on cAMP production: (a) the basal cAMP production was enhanced by a mechanism sensitive to inhibitors of calmodulin; and (b) similar to phorbol ester, cell Ca2+ caused sensitization of AC to stimulation by forskolin, an effect sensitive to Goe 6983. Decreasing cell Ca2+ below basal levels rendered AC unresponsive to stimulation by forskolin. These data suggest that a crosstalk mechanism is functional in frog ORCs, linking the sensitivity of AC to the activity of PKC. At increased activity of PKC, olfactory AC becomes more responsive to stimulation by odorants, forskolin, and cell Ca2+. Neurotransmitters appear to use this crosstalk mechanism to regulate olfactory sensitivity.
利用原位锋电位记录和放射免疫分析法,研究了神经递质对蛙嗅觉受体细胞(ORC)中cAMP介导的信号转导的影响。将卡巴胆碱应用于嗅觉上皮的黏膜侧,可增强ORC对产生cAMP的气味剂的电反应,但对未受刺激的细胞无影响。在蛋白激酶C(PKC)激活剂佛波酯(PDBu)存在的情况下,也观察到气味剂反应有类似增强。PDBu还增强了对腺苷酸环化酶(AC)激活剂福斯高林的电反应,而PKC抑制剂Goe 6983可使其减弱。卡巴胆碱、5-羟色胺和PDBu对福斯高林诱导的嗅觉组织中cAMP积累的增强作用程度相似。PKC抑制剂Goe 6983、星形孢菌素和多粘菌素B可完全抑制这种增强作用,表明PKC增加了嗅觉AC对气味剂和福斯高林刺激的敏感性。对去纤毛嗅觉组织的实验表明,AC的敏化作用仅限于ORC的感觉纤毛。为了研究细胞Ca2+对这些机制的影响,用离子霉素提高嗅觉组织的细胞内Ca2+浓度,或用BAPTA/AM降低其浓度。细胞Ca2+增加对cAMP产生有两种影响:(a)基础cAMP产生通过对钙调蛋白抑制剂敏感的机制增强;(b)与佛波酯类似,细胞Ca2+使AC对福斯高林刺激敏感,这种作用对Goe 6983敏感。将细胞Ca2+降低至基础水平以下会使AC对福斯高林刺激无反应。这些数据表明,蛙ORC中存在一种相互作用机制,将AC的敏感性与PKC的活性联系起来。在PKC活性增加时,嗅觉AC对气味剂、福斯高林和细胞Ca*2+*的刺激反应更强。神经递质似乎利用这种相互作用机制来调节嗅觉敏感性。