Biology Department, Johns Hopkins University, Baltimore, Maryland 21218, USA.
J Neurosci. 2012 Oct 17;32(42):14557-62. doi: 10.1523/JNEUROSCI.0559-12.2012.
Feedback inhibition of adenylyl cyclase III (ACIII) via Ca(2+)-induced phosphorylation has long been hypothesized to contribute to response termination and adaptation of olfactory sensory neurons (OSNs). To directly determine the functional significance of this feedback mechanism for olfaction in vivo, we genetically mutated serine(1076) of ACIII, the only residue responsible for Ca(2+)-induced phosphorylation and inhibition of ACIII (Wei et al., 1996, 1998), to alanine in mice. Immunohistochemistry and Western blot analysis showed that the mutation affects neither the cilial localization nor the expression level of ACIII in OSNs. Electroolfactogram analysis showed no differences in the responses between wild-type and mutant mice to single-pulse odorant stimulations or in several stimulation paradigms for adaptation. These results suggest that phosphorylation of ACIII on serine(1076) plays a far less important role in olfactory response attenuation than previously thought.
长期以来,人们一直假设通过 Ca(2+)诱导的磷酸化反馈抑制腺苷酸环化酶 III (ACIII)有助于嗅觉感觉神经元 (OSN) 的反应终止和适应。为了直接确定这种反馈机制对体内嗅觉的功能意义,我们在小鼠中对 ACIII 的丝氨酸(1076)进行了基因突变,该残基负责 Ca(2+)诱导的磷酸化和 ACIII 的抑制 (Wei 等人,1996,1998)。免疫组织化学和 Western blot 分析表明,该突变既不影响 ACIII 在 OSN 中的纤毛定位,也不影响其表达水平。电嗅觉图分析显示,野生型和突变型小鼠对单脉冲气味刺激的反应或几种适应刺激模式没有差异。这些结果表明,ACIII 丝氨酸(1076)上的磷酸化在嗅觉反应衰减中的作用远小于先前认为的那么重要。