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通过近红外光遗传学精确重连皮质脊髓轴突和脊髓中间神经元以治疗脊髓损伤

Precise rewiring of corticospinal axons and spinal interneurons via near-infrared optogenetics for spinal cord injury treatment.

作者信息

Ji Zhe, Yan Jun, Li Chenxi, Sun Yuhui, Wang Shoupeng, Tao Jin, Liu Jian, Liu Yaobo

机构信息

Jiangsu Key Laboratory of Drug Discovery and Translational Research for Brain Diseases, Institute of Neuroscience, Soochow University, Departments of Rehabilitation Medicine and Neurology, The Fourth Affiliated Hospital of Soochow University, Suzhou, China.

Clinical Research Center of Neurological Disease, The Second Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Sci Adv. 2025 Aug;11(31):eads4938. doi: 10.1126/sciadv.ads4938. Epub 2025 Aug 1.

Abstract

To date, precise restoration of proper connections between posttrauma axons and neurons following spinal cord injury (SCI) remains a substantial challenge. Here, we developed glutamate-linked upconversion nanoparticles (Glu-UCNP) to facilitate optogenetic control of axonal sprouting in SCI mice. After being specifically uptaken by the postsynaptic interneurons innervated by corticospinal tract (CST) axons, Glu-UCNP not only serves as internal light transducers that convert near-infrared light to visible light but also acts as nanobeacons that guide axonal sprouting toward postsynaptic neurons of glutamatergic synapses. This in situ optogenetic modulation successfully demonstrated the restoration of spinal motor circuits by rebuilding functional connections between CST axons and postsynaptic interneurons. It was corroborated by live-cell recording, immunofluorescence staining, in vivo Ca imaging, and pellet-reaching tests. Transcriptome sequencing further elucidated the molecular network changes underlying this optogenetic modulation. These findings highlight the potential therapeutic applications of optogenetic modulation in the reassembly of neural circuits after SCI.

摘要

迄今为止,脊髓损伤(SCI)后创伤后轴突与神经元之间正确连接的精确恢复仍然是一项重大挑战。在此,我们开发了谷氨酸连接的上转换纳米颗粒(Glu-UCNP),以促进对SCI小鼠轴突发芽的光遗传学控制。在被皮质脊髓束(CST)轴突支配的突触后中间神经元特异性摄取后,Glu-UCNP不仅作为将近红外光转换为可见光的内部光传感器,还作为引导轴突发芽朝向谷氨酸能突触的突触后神经元的纳米信标。这种原位光遗传学调制成功地通过重建CST轴突与突触后中间神经元之间的功能连接,证明了脊髓运动回路的恢复。活细胞记录、免疫荧光染色、体内钙成像和抓握试验证实了这一点。转录组测序进一步阐明了这种光遗传学调制背后的分子网络变化。这些发现突出了光遗传学调制在SCI后神经回路重组中的潜在治疗应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892a/12315976/297f6b4a9643/sciadv.ads4938-f1.jpg

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