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Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury

Spinal cord injury (SCI) involves diverse injury responses in different cell types in a temporally and spatially specific manner. Here, using single-cell transcriptomic analyses combined with classic anatomical, behavioral, electrophysiological analyses, we report, with single-cell resolution, tempo...

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Detalles Bibliográficos
Autores principales: Li, Chen, Wu, Zhourui, Zhou, Liqiang, Shao, Jingliang, Hu, Xiao, Xu, Wei, Ren, Yilong, Zhu, Xingfei, Ge, Weihong, Zhang, Kunshan, Liu, Jiping, Huang, Runzhi, Yu, Jing, Luo, Dandan, Yang, Xuejiao, Zhu, Wenmin, Zhu, Rongrong, Zheng, Changhong, Sun, Yi Eve, Cheng, Liming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888618/
https://www.ncbi.nlm.nih.gov/pubmed/35232960
http://dx.doi.org/10.1038/s41392-022-00885-4
Descripción
Sumario:Spinal cord injury (SCI) involves diverse injury responses in different cell types in a temporally and spatially specific manner. Here, using single-cell transcriptomic analyses combined with classic anatomical, behavioral, electrophysiological analyses, we report, with single-cell resolution, temporal molecular and cellular changes in crush-injured adult mouse spinal cord. Data revealed pathological changes of 12 different major cell types, three of which infiltrated into the spinal cord at distinct times post-injury. We discovered novel microglia and astrocyte subtypes in the uninjured spinal cord, and their dynamic conversions into additional stage-specific subtypes/states. Most dynamic changes occur at 3-days post-injury and by day-14 the second wave of microglial activation emerged, accompanied with changes in various cell types including neurons, indicative of the second round of attacks. By day-38, major cell types are still substantially deviated from uninjured states, demonstrating prolonged alterations. This study provides a comprehensive mapping of cellular/molecular pathological changes along the temporal axis after SCI, which may facilitate the development of novel therapeutic strategies, including those targeting microglia.