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同时缺失Pten和Socs3的成年受损视网膜轴突与视交叉上核神经元形成活跃突触。

Injured adult retinal axons with Pten and Socs3 co-deletion reform active synapses with suprachiasmatic neurons.

作者信息

Li Songshan, He Qinghai, Wang Hao, Tang Xuming, Ho Kam Wing, Gao Xin, Zhang Qian, Shen Yang, Cheung Annie, Wong Francis, Wong Yung Hou, Ip Nancy Y, Jiang Liwen, Yung Wing Ho, Liu Kai

机构信息

Division of Life Science, State Key Laboratory of Molecular Neuroscience, School of Science and Institute for Advance Study, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China; Center of Systems Biology and Human Health, School of Science and Institute for Advance Study, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China.

School of Life Sciences, Centre for Cell and Developmental Biology and State Key Laboratory of Agrobiotechnology, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.

出版信息

Neurobiol Dis. 2015 Jan;73:366-76. doi: 10.1016/j.nbd.2014.09.019. Epub 2014 Oct 16.

Abstract

Despite advances in promoting axonal regeneration after adult central nervous system injury, elicitation of a large number of lesion-passing axons reform active synaptic connections with natural target neurons remains limited. By deleting both Pten and Socs3 in retinal ganglion cells, we report that optic nerve axons after prechiasm lesion robustly reinnervate the hypothalamus, form new synapses with neurons in the suprachiasmatic nucleus (SCN), and re-integrate with the existing circuitry. Photic or electric stimulation of the retinal axons induces neuronal response in SCN. However both the innervation pattern and evoked responses are not completely restored by the regenerating axons, suggesting that combining with other strategies is necessary to overcome the defective rewiring. Our results support that boosting the intrinsic growth capacity in injured neurons promotes axonal reinnervation and rewiring.

摘要

尽管在促进成体中枢神经系统损伤后轴突再生方面取得了进展,但诱导大量穿过损伤部位的轴突与天然靶神经元重新形成活跃的突触连接仍然有限。通过删除视网膜神经节细胞中的Pten和Socs3,我们报告称,视交叉前损伤后的视神经轴突有力地重新支配下丘脑,与视交叉上核(SCN)中的神经元形成新的突触,并与现有神经回路重新整合。对视网膜轴突进行光刺激或电刺激可诱导SCN中的神经元反应。然而,再生轴突并未完全恢复神经支配模式和诱发反应,这表明有必要结合其他策略来克服有缺陷的重新布线。我们的结果支持,增强受损神经元的内在生长能力可促进轴突重新支配和重新布线。

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