Kaur R, Zhu X O, Moorhouse A J, Barry P H
School of Physiology and Pharmacology, The University of New South Wales, Sydney 2052, Australia.
J Membr Biol. 2001 May 15;181(2):91-105.
Olfactory receptor neurons respond to odorants with G protein-mediated increases in the concentrations of cyclic adenosine 3',5'-monophosphate (cAMP) and/or inositol-1,4,5-trisphosphate (IP3). This study provides evidence that both second messengers can directly activate distinct ion channels in excised inside-out patches from the dendritic knob and soma membrane of rat olfactory receptor neurons (ORNs). The IP3-gated channels in the dendritic knob and soma membranes could be classified into two types, with conductances of 40 +/- 7 pS (n = 5) and 14 +/- 3 pS (n = 4), with the former having longer open dwell times. Estimated values of the densities of both channels from the same inside-out membrane patches were very much smaller for IP3-gated than for CNG channels. For example, in the dendritic knob membrane there were about 1000 CNG channels x microm(-2) compared to about 85 IP3-gated channels x microm(-2). Furthermore, only about 36% of the dendritic knob patches responded to IP3, whereas 83% of the same patches responded to cAMP. In the soma, both channel densities were lower, with the CNG channel density again being larger ( approximately 57 channels x microm(-2)) than that of the IP3-gated channels ( approximately 13 channels x microm(-2)), with again a much smaller fraction of patches responding to IP3 than to cAMP. These results were consistent with other evidence suggesting that the cAMP-pathway dominates the IP3 pathway in mammalian olfactory transduction.
嗅觉受体神经元通过G蛋白介导,对气味剂做出反应,使环磷酸腺苷(cAMP)和/或肌醇-1,4,5-三磷酸(IP3)的浓度增加。本研究提供了证据表明,这两种第二信使都可以直接激活从大鼠嗅觉受体神经元(ORN)的树突状小体和体细胞膜上切除的内向外膜片中的不同离子通道。树突状小体和体细胞膜中的IP3门控通道可分为两种类型,电导分别为40±7 pS(n = 5)和14±3 pS(n = 4),前者具有更长的开放驻留时间。从相同的内向外膜片中估计,IP3门控通道的密度值比环核苷酸门控(CNG)通道的密度值小得多。例如,在树突状小体膜中,每平方微米约有1000个CNG通道,而每平方微米约有85个IP3门控通道。此外,只有约36%的树突状小体膜片对IP3有反应,而83%的相同膜片对cAMP有反应。在体细胞中,两种通道的密度都较低,CNG通道密度(约57个通道/平方微米)再次大于IP3门控通道密度(约13个通道/平方微米),对IP3有反应的膜片比例也再次远小于对cAMP有反应的膜片比例。这些结果与其他证据一致,表明在哺乳动物嗅觉转导中,cAMP途径主导IP3途径。