中国神经再生研究(英文版) ›› 2023, Vol. 18 ›› Issue (4): 913-921.doi: 10.4103/1673-5374.353852

• 原著:视神经损伤修复保护与再生 • 上一篇    下一篇

透明化处理联合逆向跨突触病毒示踪分析视神经挤压小鼠大脑中视网膜受体区域的变化

  

  • 出版日期:2023-04-15 发布日期:2022-10-29
  • 基金资助:
    国家自然科学基金项目(81870655)

Use of a tissue clearing technique combined with retrograde trans-synaptic viral tracing to evaluate changes in mouse retinorecipient brain regions following optic nerve crush

Zong-Yi Zhan1, #, Yi-Ru Huang2, #, Lu-Wei Zhao3, Ya-Dan Quan4, 5, Zi-Jing Li1, Di-Fang Sun1, Ya-Li Wu6, Hao-Yuan Wu3, Zi-Tian Liu2, Kai-Li Wu2, Yu-Qing Lan1, *, Min-Bin Yu2, *#br#   

  1. 1Department 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;  2State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong Province, China;  3Light Innovation Technology Ltd., Hong Kong Special Administrative Region, China;  4Department of Ophthalmology & Visual Science, Shanghai Medical College, Fudan University, Shanghai, China;  5Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China;  6Department of Ophthalmology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, China
  • Online:2023-04-15 Published:2022-10-29
  • Contact: Min-Bin Yu, MD, PhD, yuminbin@mail.sysu.edu.cn; Yu-Qing Lan, MD, PhD, lanyq@mail.sysu.edu.cn.
  • Supported by:
    This study was supported by the National Natural Science Foundation of China, No. 81870655 (to MBY). 

摘要:

成功建立视网膜神经节细胞和大脑中视网膜受体区域之间的重新连接是评估视神经再生的关键。然而,由于脑组织不是透明的,因此观察视网膜受体区域的形态并不容易。实验创新性地结合了组织透明化技术和逆向跨突触病毒示踪技术观察小鼠视神经损伤后视网膜神经节细胞的脑内视网膜投射区域的变化。光片显微镜对透明化处理后的全脑组织进行成像,结果发现伪狂犬病毒(PRV724)主要感染视网膜神经节细胞,并可在透明化大脑中逆行示踪视网膜受体区域,同时PRV724示踪的神经元比同类研究更广泛。同时发现,视神经损伤可选择性减少PRV724标记的视网膜神经节细胞在下丘脑室旁核、膝状叶间核、腹侧外侧膝状核、杏仁核中央、杏仁核基底外侧、Edinger-Westphal核和动眼神经核的投射,而不影响前庭上核、红核、蓝斑、巨细胞网状核和面神经核的投射。这一结果提示,组织透明化技术联合逆向跨突触病毒示踪技术可更客观和整体的评估小鼠视神经损伤后视网膜神经节细胞的脑内视网膜投射区域的变化,这为评估视神经损伤和再生提供了一种可行的方法。

http://orcid.org/0000-0002-3938-7164 (Min-Bin Yu); 

http://orcid.org/0000-0001-7615-5648 (Yu-Qing Lan); 

https://orcid.org/0000-0002-6621-1172 (Zong-Yi Zhan); 
http://orcid.org/0000-0002-3761-6111 (Zi-Jing Li); 

https://orcid.org/0000-0002-8443-4740 (Di-Fang Sun); 

http://orcid.org/0000-0002-3449-1843 (Ya-Li Wu); 
http://orcid.org/0000-0002-8170-0265 (Zi-Tian Liu); 

http://orcid.org/0000-0003-3606-683X (Kai-Li Wu)

关键词: 视神经挤压, 视网膜神经节细胞, 组织透明化, 组织学, 三维成像, 图像分析, 伪狂犬病毒, 病毒示踪, 全脑研究, 光学成像

Abstract: 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.

Key words: histology, image analysis, light-sheet imaging, optic nerve crush, pseudorabies virus, retinal ganglion cells, three-dimensional imaging, tissue clearing, viral tracing, whole brain study