Stanek Edward, Rodriguez Erica, Zhao Shengli, Han Bao-Xia, Wang Fan
Departments of Neurobiology and.
Departments of Neurobiology and Cell Biology, Duke University Medical Center, Durham, North Carolina 27710
J Neurosci. 2016 Jul 20;36(29):7663-75. doi: 10.1523/JNEUROSCI.0839-16.2016.
Anatomical studies have identified brainstem neurons that project bilaterally to left and right oromotor pools, which could potentially mediate bilateral muscle coordination. We use retrograde lentiviruses combined with a split-intein-mediated split-Cre-recombinase system in mice to isolate, characterize, and manipulate a population of neurons projecting to both the left and right jaw-closing trigeminal motoneurons. We find that these bilaterally projecting premotor neurons (BPNs) reside primarily in the supratrigeminal nucleus (SupV) and the parvicellular and intermediate reticular regions dorsal to the facial motor nucleus. These BPNs also project to multiple midbrain and brainstem targets implicated in orofacial sensorimotor control, and consist of a mix of glutamatergic, GABAergic, and glycinergic neurons, which can drive both excitatory and inhibitory inputs to trigeminal motoneurons when optogenetically activated in slice. Silencing BPNs with tetanus toxin light chain (TeNT) increases bilateral masseter activation during chewing, an effect driven by the expression of TeNT in SupV BPNs. Acute unilateral optogenetic inhibition of SupV BPNs identifies a group of tonically active neurons that function to lower masseter muscle tone, whereas unilateral optogenetic activation of SupV BPNs is sufficient to induce bilateral masseter activation both during resting state and during chewing. These results provide evidence for SupV BPNs in tonically modulating jaw-closing muscle tone and in mediating bilateral jaw closing.
We developed a method that combines retrograde lentiviruses with the split-intein-split-Cre system in mice to isolate, characterize, and manipulate neurons that project to both left and right jaw-closing motoneurons. We show that these bilaterally projecting premotor neurons (BPNs) reside primarily in the supratrigeminal nucleus and the rostral parvicellular and intermediate reticular nuclei. BPNs consist of both excitatory and inhibitory populations, and also project to multiple brainstem nuclei implicated in orofacial sensorimotor control. Manipulation of the supratrigeminal BPNs during natural jaw-closing behavior reveals a dual role for these neurons in eliciting phasic muscle activation and in maintaining basal muscle tone. The retrograde lentivirus carrying the split-intein-split-Cre system can be applied to study any neurons with bifurcating axons innervating two brain regions.
解剖学研究已确定了向左右口面部运动核双侧投射的脑干神经元,这些神经元可能介导双侧肌肉协调。我们在小鼠中使用逆行慢病毒结合分裂内含肽介导的分裂Cre重组酶系统,来分离、表征和操纵一群向左右两侧下颌闭合三叉运动神经元投射的神经元。我们发现,这些双侧投射的运动前神经元(BPN)主要位于三叉上核(SupV)以及面神经运动核背侧的小细胞和中间网状区域。这些BPN还投射到多个与口面部感觉运动控制相关的中脑和脑干靶点,并且由谷氨酸能、γ-氨基丁酸能和甘氨酸能神经元混合组成,当在脑片中进行光遗传学激活时,它们可以驱动对三叉运动神经元的兴奋性和抑制性输入。用破伤风毒素轻链(TeNT)使BPN沉默会增加咀嚼过程中双侧咬肌的激活,这种效应是由SupV BPN中TeNT的表达所驱动的。对SupV BPN进行急性单侧光遗传学抑制可识别出一组具有紧张性活动的神经元,其功能是降低咬肌肌张力,而对SupV BPN进行单侧光遗传学激活足以在静息状态和咀嚼过程中诱导双侧咬肌激活。这些结果为SupV BPN在紧张性调节下颌闭合肌张力和介导双侧下颌闭合方面提供了证据。
我们开发了一种方法,将逆行慢病毒与小鼠中的分裂内含肽 - 分裂Cre系统相结合,以分离、表征和操纵向左右两侧下颌闭合运动神经元投射的神经元。我们表明,这些双侧投射的运动前神经元(BPN)主要位于三叉上核以及嘴侧小细胞和中间网状核。BPN由兴奋性和抑制性群体组成,并且还投射到多个与口面部感觉运动控制相关的脑干核。在自然下颌闭合行为期间对三叉上BPN进行操纵,揭示了这些神经元在引发阶段性肌肉激活和维持基础肌肉张力方面的双重作用。携带分裂内含肽 - 分裂Cre系统的逆行慢病毒可用于研究任何轴突分叉并支配两个脑区的神经元。