Wray S, Fueshko S M, Kusano K, Gainer H
Laboratory of Neurochemistry, National Institutes of Health, Bethesda, Maryland, 20892, USA.
Dev Biol. 1996 Dec 15;180(2):631-45. doi: 10.1006/dbio.1996.0334.
In previous work, we showed a robust gamma-aminobutyric acid (GABAergic) synaptic input onto embryonic luteinizing hormone-releasing hormone (LHRH) neurons maintained in olfactory explants. In this study, we identify GABAergic neurons in olfactory pit (OP) of embryonic mice in vivo and study, using patch-pipet whole-cell current and voltage clamp techniques, synaptic interactions of these neurons in explant cultures. In vivo, glutamate decarboxylase (GAD, the enzyme which synthesizes GABA) mRNA was first detected in nasal regions on Embryonic Day (E) 11.5. From E12.5 to E13.5, robust GAD expression was localized to cells primarily in the ventral aspect of the OP. GAD mRNA was not detected over dorsally located cells in olfactory sensory or respiratory epithelium. In addition, GAD mRNA was not observed in cells along olfactory axons. GAD mRNA was dramatically reduced in the OP/vomeronasal organ by E16.5. Using antibodies against both GABA and GAD, immunopositive axonal-like tracts were detected in the nasal septum on E12.5. GABAergic staining decreased by E13.5. To examine synaptic interactions of these GABAergic cells, embryonic olfactory explants were generated and maintained in serum-free media. As explants spread, neuron-like cells migrated into the periphery, sometimes forming ganglion-like clusters. Cells were recorded, marked intracellularly with Lucifer Yellow and post-fixation, immunocytochemically examined. Forty-six cells, typically multipolar, were GABAergic, had resting potentials around -50 mV, and exhibited spontaneous action potentials which were generated by spontaneous depolarizing GABAergic (GABAA) synaptic activity. OP neurons depolarized in response to GABA by increasing Cl- conductance. The biophysical properties of OP-derived GABAergic neurons were distinct from those reported for olfactory receptor neurons but similar to embryonic LHRH neurons. However, unlike LHRH neurons, GABAergic neurons did not migrate large distances in olfactory explants or appear to leave the olfactory pit in vivo.
在之前的研究中,我们发现,在嗅觉外植体中培养的胚胎促黄体生成素释放激素(LHRH)神经元上存在强大的γ-氨基丁酸(GABA能)突触输入。在本研究中,我们在体内鉴定了胚胎小鼠嗅窝(OP)中的GABA能神经元,并使用膜片吸管全细胞电流和电压钳技术,研究了这些神经元在外植体培养物中的突触相互作用。在体内,谷氨酸脱羧酶(GAD,合成GABA的酶)mRNA在胚胎第(E)11.5天首次在鼻区被检测到。从E12.5到E13.5,强大的GAD表达定位于主要在OP腹侧的细胞。在嗅觉感觉或呼吸上皮背侧的细胞中未检测到GAD mRNA。此外,在嗅觉轴突沿线的细胞中未观察到GAD mRNA。到E16.5时,OP/犁鼻器中的GAD mRNA显著减少。使用针对GABA和GAD的抗体,在E12.5时在鼻中隔中检测到免疫阳性的轴突样束。GABA能染色在E13.5时减少。为了检查这些GABA能细胞的突触相互作用,制备了胚胎嗅觉外植体并在无血清培养基中培养。随着外植体的扩展,神经元样细胞迁移到周边,有时形成神经节样簇。对细胞进行记录,用荧光黄进行细胞内标记,固定后进行免疫细胞化学检查。46个细胞通常为多极,是GABA能的,静息电位约为-50 mV,并表现出自发性动作电位,这些动作电位由自发性去极化GABA能(GABAA)突触活动产生。OP神经元通过增加Cl-电导对GABA作出反应而发生去极化。源自OP的GABA能神经元的生物物理特性与嗅觉受体神经元报道的不同,但与胚胎LHRH神经元相似。然而,与LHRH神经元不同,GABA能神经元在嗅觉外植体中不会远距离迁移,在体内也似乎不会离开嗅窝。