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

Chen Li(Tongji University), Zhourui Wu(Tongji University), Liqiang Zhou(Tongji University), Jingliang Shao(Tongji University), Xiao Hu(Tongji University), Wei Xu(Tongji University), Yilong Ren(Tongji University), Xingfei Zhu(Tongji University), Weihong Ge(University of California, Los Angeles), Kunshan Zhang(Tongji University), Jiping Liu(Tongji University), Runzhi Huang(Tongji University), Jing Yu(Tongji University), Dandan Luo(Tongji University), Xuejiao Yang(Tongji University), Wenmin Zhu(Tongji University), Rongrong Zhu(Tongji University), Changhong Zheng(Tongji University), Yi Sun(Tongji University), Liming Cheng(Tongji University)
Signal Transduction and Targeted Therapy
March 2, 2022
Cited by 235Open Access
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Abstract

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.


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