Wang Ze-Jun, Sun Liqin, Heinbockel Thomas
Department of Anatomy, Howard University College of Medicine, Washington, DC 20059, USA.
Department of Pharmacology and Physiology, Georgetown University Medical Center, Washington, DC 20057, USA.
Brain Sci. 2024 Jul 3;14(7):678. doi: 10.3390/brainsci14070678.
Mitral cells (MCs) in the main olfactory bulb relay odor information to higher-order olfactory centers by encoding the information in the form of action potentials. The firing patterns of these cells are influenced by both their intrinsic properties and their synaptic connections within the neural network. However, reports on MC firing patterns have been inconsistent, and the mechanisms underlying these patterns remain unclear. Using whole-cell patch-clamp recordings in mouse brain slices, we discovered that MCs exhibit two types of integrative behavior: regular/rhythmic firing and bursts of action potentials. These firing patterns could be transformed both spontaneously and chemically. MCs with regular firing maintained their pattern even in the presence of blockers of fast synaptic transmission, indicating this was an intrinsic property. However, regular firing could be transformed into bursting by applying GABA receptor antagonists to block inhibitory synaptic transmission. Burst firing could be reverted to regular firing by blocking ionotropic glutamate receptors, rather than applying a GABA receptor agonist, indicating that ionotropic glutamatergic transmission mediated this transformation. Further experiments on long-lasting currents (LLCs), which generated burst firing, also supported this mechanism. In addition, cytoplasmic Ca in MCs was involved in the transformation of firing patterns mediated by glutamatergic transmission. Metabotropic glutamate receptors also played a role in LLCs in MCs. These pieces of evidence indicate that odor information can be encoded on a mitral cell (MC) platform, where it can be relayed to higher-order olfactory centers through intrinsic and dendrodendritic mechanisms in MCs.
主嗅球中的二尖瓣细胞(MCs)通过以动作电位的形式编码信息,将气味信息传递到高阶嗅觉中枢。这些细胞的放电模式受其内在特性及其在神经网络中的突触连接的影响。然而,关于MC放电模式的报道并不一致,这些模式背后的机制仍不清楚。通过在小鼠脑片中进行全细胞膜片钳记录,我们发现MCs表现出两种整合行为:规则/节律性放电和动作电位爆发。这些放电模式可以自发地和通过化学方式进行转换。具有规则放电的MCs即使在存在快速突触传递阻滞剂的情况下也能保持其模式,这表明这是一种内在特性。然而,通过应用GABA受体拮抗剂来阻断抑制性突触传递,可以将规则放电转换为爆发性放电。通过阻断离子型谷氨酸受体而不是应用GABA受体激动剂,可以将爆发性放电恢复为规则放电,这表明离子型谷氨酸能传递介导了这种转换。对产生爆发性放电的长时程电流(LLCs)的进一步实验也支持了这一机制。此外,MCs中的细胞质Ca参与了由谷氨酸能传递介导的放电模式转换。代谢型谷氨酸受体在MCs的LLCs中也发挥了作用。这些证据表明,气味信息可以在二尖瓣细胞(MC)平台上进行编码,在该平台上,气味信息可以通过MCs中的内在机制和树突-树突机制传递到高阶嗅觉中枢。