Yuan Man, Tan Gao, Cai Danrui, Luo Xue, Shen Kejiong, Deng Qinqin, Lei Xinlan, Zeng Wen-Bo, Luo Min-Hua, Huang Lu, Ren Chaoran, Shen Yin
Eye Center, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, 430060, Hubei, China.
State Key Laboratory of Virology, CAS Center for Excellence in Brain Science and Intelligence Technology, Wuhan Institute of Virology, Wuhan, 430071, China.
Neurosci Bull. 2024 Dec;40(12):1886-1900. doi: 10.1007/s12264-024-01295-y. Epub 2024 Sep 16.
The looming stimulus-evoked flight response to approaching predators is a defensive behavior in most animals. However, how looming stimuli are detected in the retina and transmitted to the brain remains unclear. Here, we report that a group of GABAergic retinal ganglion cells (RGCs) projecting to the superior colliculus (SC) transmit looming signals from the retina to the brain, mediating the looming-evoked flight behavior by releasing GABA. GAD2-Cre and vGAT-Cre transgenic mice were used in combination with Cre-activated anterograde or retrograde tracer viruses to map the inputs to specific GABAergic RGC circuits. Optogenetic technology was used to assess the function of SC-projecting GABAergic RGCs (scpgRGCs) in the SC. FDIO-DTA (Flp-dependent Double-Floxed Inverted Open reading frame-Diphtheria toxin) combined with the FLP (Florfenicol, Lincomycin & Prednisolone) approach was used to ablate or silence scpgRGCs. In the mouse retina, GABAergic RGCs project to different brain areas, including the SC. ScpgRGCs are monosynaptically connected to parvalbumin-positive SC neurons known to be required for the looming-evoked flight response. Optogenetic activation of scpgRGCs triggers GABA-mediated inhibition in SC neurons. Ablation or silencing of scpgRGCs compromises looming-evoked flight responses without affecting image-forming functions. Our study reveals that scpgRGCs control the looming-evoked flight response by regulating SC neurons via GABA, providing novel insight into the regulation of innate defensive behaviors.
对逼近的捕食者产生的迫近刺激诱发的逃避反应是大多数动物的一种防御行为。然而,视网膜如何检测到迫近刺激并将其传递到大脑仍不清楚。在这里,我们报告称,一组投射到上丘(SC)的γ-氨基丁酸能视网膜神经节细胞(RGCs)将迫近信号从视网膜传递到大脑,通过释放γ-氨基丁酸介导迫近诱发的逃避行为。GAD2-Cre和vGAT-Cre转基因小鼠与Cre激活的顺行或逆行示踪病毒联合使用,以绘制特定γ-氨基丁酸能RGC回路的输入。光遗传学技术用于评估投射到SC的γ-氨基丁酸能RGCs(scpgRGCs)在上丘中的功能。FDIO-DTA(Flp依赖性双loxed反向开放阅读框-白喉毒素)与FLP(氟苯尼考、林可霉素和泼尼松龙)方法联合使用,以消融或沉默scpgRGCs。在小鼠视网膜中,γ-氨基丁酸能RGCs投射到包括上丘在内的不同脑区。ScpgRGCs与已知的迫近诱发逃避反应所需的小白蛋白阳性上丘神经元单突触连接。光遗传学激活scpgRGCs会触发上丘神经元中γ-氨基丁酸介导的抑制作用。消融或沉默scpgRGCs会损害迫近诱发逃避反应,而不影响成像功能。我们的研究表明,scpgRGCs通过γ-氨基丁酸调节上丘神经元来控制迫近诱发的逃避反应,为先天防御行为的调节提供了新的见解。