Zhan Zong-Yi, Huang Yi-Ru, Zhao Lu-Wei, Quan Ya-Dan, Li Zi-Jing, Sun Di-Fang, Wu Ya-Li, Wu Hao-Yuan, Liu Zi-Tian, Wu Kai-Li, Lan Yu-Qing, Yu Min-Bin
Department of Ophthalmology, Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong Province, China.
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong Province, China.
Neural Regen Res. 2023 Apr;18(4):913-921. doi: 10.4103/1673-5374.353852.
Successful establishment of reconnection between retinal ganglion cells and retinorecipient regions in the brain is critical to optic nerve regeneration. However, morphological assessments of retinorecipient regions are limited by the opacity of brain tissue. In this study, we used an innovative tissue cleaning technique combined with retrograde trans-synaptic viral tracing to observe changes in retinorecipient regions connected to retinal ganglion cells in mice after optic nerve injury. Specifically, we performed light-sheet imaging of whole brain tissue after a clearing process. We found that pseudorabies virus 724 (PRV724) mostly infected retinal ganglion cells, and that we could use it to retrogradely trace the retinorecipient regions in whole tissue-cleared brains. Unexpectedly, PRV724-traced neurons were more widely distributed compared with data from previous studies. We found that optic nerve injury could selectively modify projections from retinal ganglion cells in the hypothalamic paraventricular nucleus, intergeniculate leaflet, ventral lateral geniculate nucleus, central amygdala, basolateral amygdala, Edinger-Westphal nucleus, and oculomotor nucleus, but not the superior vestibular nucleus, red nucleus, locus coeruleus, gigantocellular reticular nucleus, or facial nerve nucleus. Our findings demonstrate that the tissue clearing technique, combined with retrograde trans-synaptic viral tracing, can be used to objectively and comprehensively evaluate changes in mouse retinorecipient regions that receive projections from retinal ganglion cells after optic nerve injury. Thus, our approach may be useful for future estimations of optic nerve injury and regeneration.
视网膜神经节细胞与大脑中视网膜接收区域之间成功重建连接对视神经再生至关重要。然而,视网膜接收区域的形态学评估受到脑组织不透明度的限制。在本研究中,我们使用了一种创新的组织清理技术并结合逆行跨突触病毒示踪,以观察视神经损伤后小鼠中与视网膜神经节细胞相连的视网膜接收区域的变化。具体而言,我们在清理过程后对全脑组织进行了光片成像。我们发现伪狂犬病病毒724(PRV724)主要感染视网膜神经节细胞,并且我们可以用它来逆行追踪全组织清理大脑中的视网膜接收区域。出乎意料的是,与先前研究的数据相比,PRV724追踪的神经元分布更广泛。我们发现视神经损伤可选择性地改变来自视网膜神经节细胞在下丘脑室旁核、间膝叶、腹侧外侧膝状核、中央杏仁核、基底外侧杏仁核、动眼神经核和动眼神经核的投射,但不改变前庭上核、红核、蓝斑、巨细胞网状核或面神经核的投射。我们的研究结果表明,组织清理技术与逆行跨突触病毒示踪相结合,可用于客观、全面地评估视神经损伤后从小鼠视网膜神经节细胞接收投射的视网膜接收区域的变化。因此,我们的方法可能有助于未来对视神经损伤和再生的评估。