Movahedi Kiavash, Grosmaitre Xavier, Feinstein Paul
Max Planck Institute of Biophysics, Max-von-Laue-Strasse 3, 60438 Frankfurt, Germany Myeloid Cell Immunology Laboratory, VIB Inflammation Research Center, Ghent, Belgium Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, Belgium
Centre des Sciences du Goût et de l'Alimentation, CNRS, INRA, Université Bourgogne Franche-Comté, 21000 Dijon, France.
Open Biol. 2016 Jul;6(7). doi: 10.1098/rsob.160018.
Odorant receptors (ORs) control several aspects of cell fate in olfactory sensory neurons (OSNs), including singular gene choice and axonal identity. The mechanisms of OR-induced axon guidance have been suggested to principally rely on G-protein signalling. Here, we report that for a subset of OSNs, deleting G proteins or altering their levels of signalling does not affect axonal identity. Signalling-deficient ORs or surrogate receptors that are unable to couple to Gs/Golf still provide axons with distinct identities and the anterior-posterior targeting of axons does not correlate with the levels of cAMP produced by genetic modifications. In addition, we refine the models of negative feedback by showing that ectopic ORs can be robustly expressed without suppressing endogenous gene choice. In conclusion, our results uncover a new feature of ORs, showing that they can instruct axonal identity and regulate olfactory map formation independent of canonical G-protein signalling and cAMP production.
嗅觉受体(ORs)控制嗅觉感觉神经元(OSNs)中细胞命运的多个方面,包括单一基因选择和轴突身份。OR诱导的轴突导向机制主要被认为依赖于G蛋白信号传导。在这里,我们报告,对于一部分OSNs,删除G蛋白或改变其信号水平不会影响轴突身份。缺乏信号传导的ORs或无法与Gs/Golf偶联的替代受体仍然为轴突提供不同的身份,并且轴突的前后靶向与基因修饰产生的cAMP水平无关。此外,我们通过表明异位ORs可以在不抑制内源性基因选择的情况下稳健表达来完善负反馈模型。总之,我们的结果揭示了ORs的一个新特征,表明它们可以独立于经典G蛋白信号传导和cAMP产生来指导轴突身份并调节嗅觉图谱形成。