Department of Neurology, Baylor College of Medicine, Houston, TX 77030.
Department of Neurology, Baylor College of Medicine, Houston, TX 77030
eNeuro. 2022 Oct 17;9(5). doi: 10.1523/ENEURO.0093-22.2022. Print 2022 Sep-Oct.
The Emx1-IRES-Cre transgenic mouse is commonly used to direct genetic recombination in forebrain excitatory neurons. However, the original study reported that Emx1-Cre is also expressed embryonically in peripheral autonomic ganglia, which could potentially affect the interpretation of targeted circuitry contributing to systemic phenotypes. Here, we report that Emx1-Cre is expressed in the afferent vagus nerve system involved in autonomic cardiorespiratory regulatory pathways. Our imaging studies revealed expression of Emx1-Cre driven tdtomato fluorescence in the afferent vagus nerve innervating the dorsal medulla of brainstem, cell bodies in the nodose ganglion, and their potential target structures at the carotid bifurcation such as the carotid sinus and the superior cervical ganglion (SCG). Photostimulation of the afferent terminals in the nucleus tractus solitarius (NTS) using Emx1-Cre driven ChR2 reliably evoked EPSCs in the postsynaptic neurons with electrophysiological characteristics consistent with the vagus afferent nerves. In addition, optogenetic stimulation targeting the Emx1-Cre expressing structures identified in this study, such as vagus nerve, carotid bifurcation, and the dorsal medulla surface transiently depressed cardiorespiratory rate in urethane anesthetized mice Together, our study demonstrates that Emx1-IRES-Cre is expressed in the key peripheral autonomic nerve system and can modulate cardiorespiratory function independently of forebrain expression. These results raise caution when interpreting systemic phenotypes of Emx1-IRES-Cre conditional recombinant mice, and also suggest the utility of this line to investigate modulators of the afferent vagal system.
Emx1-IRES-Cre 转基因小鼠常用于指导前脑兴奋性神经元中的基因重组。然而,原始研究报告称 Emx1-Cre 也在胚胎期表达于外周自主神经节,这可能会影响对参与系统性表型的靶向回路的解释。在这里,我们报告 Emx1-Cre 在参与自主心血管调节途径的传入迷走神经系统中表达。我们的成像研究显示,Emx1-Cre 驱动的 tdtomato 荧光在支配脑干背侧的传入迷走神经、结状神经节中的细胞体及其在颈动脉分叉处的潜在靶结构(如颈动脉窦和颈上交感神经节(SCG))中表达。使用 Emx1-Cre 驱动的 ChR2 对孤束核(NTS)中的传入末端进行光刺激,可靠地在具有与迷走传入神经一致的电生理特征的突触后神经元中诱发 EPSC。此外,针对本研究中鉴定的 Emx1-Cre 表达结构(如迷走神经、颈动脉分叉和背侧脑干表面)进行光遗传刺激,可短暂地降低乌拉坦麻醉小鼠的心肺呼吸频率。总之,我们的研究表明,Emx1-IRES-Cre 表达于关键的外周自主神经系统,并可独立于前脑表达来调节心肺功能。这些结果在解释 Emx1-IRES-Cre 条件性重组小鼠的系统性表型时需要谨慎,并且还提示该线可用于研究传入迷走神经系统的调节剂。