| First Author | Kolling LJ | Year | 2025 |
| Journal | J Cell Sci | Volume | 138 |
| Issue | 19 | PubMed ID | 40969102 |
| Mgi Jnum | J:376455 | Mgi Id | MGI:8257526 |
| Doi | 10.1242/jcs.264088 | Citation | Kolling LJ, et al. (2025) The superficial tufted and mitral cell output neurons of the mouse olfactory bulb have dual roles in insulin sensing. J Cell Sci 138(19):jcs264088 |
| abstractText | The olfactory bulb (OB) contains multiple parallel projection neurons to relay the nature of a stimulus. In a mouse ex vivo slice preparation, we used patch-clamp electrophysiology to measure intrinsic properties, excitability, action potential (AP) shape, voltage-activated conductances and neuromodulation in the newly categorized superficial tufted cells (sTCs) compared with those of mitral cells (MCs). We propose that a marked difference in voltage-dependent current represents distinct ion channel populations that affect the kinetics of action potentials and evokes an increase in sTC firing frequency, despite both types of projection neurons having similar AP spiking activity. Triple-colored immunofluorescence and RNA scope were used to detect colocalization of the Kv1.3 ion channel and the insulin receptor in sTCs, with approximately 73% of sTCs expressing both. The sTCs were modulated by bath application of insulin - increasing AP firing frequency by 97%, attributable to an 8% decrease in the intraburst interval, and a reduction of the latency to first spike by 37%. We conclude that there might be a range of neuromodulators of sTCs that can alter excitability and fine-tune olfactory information processing or metabolic balance. |
