Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784661199185510400 |
---|---|
author | 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 |
author_facet | 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 |
author_sort | Li, Chen |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8888618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88886182022-03-17 Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury 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 Signal Transduct Target Ther Article 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. Nature Publishing Group UK 2022-03-02 /pmc/articles/PMC8888618/ /pubmed/35232960 http://dx.doi.org/10.1038/s41392-022-00885-4 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article 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 Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury |
title | Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury |
title_full | Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury |
title_fullStr | Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury |
title_full_unstemmed | Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury |
title_short | Temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury |
title_sort | temporal and spatial cellular and molecular pathological alterations with single-cell resolution in the adult spinal cord after injury |
topic | Article |
url | 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 |
work_keys_str_mv | AT lichen temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT wuzhourui temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT zhouliqiang temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT shaojingliang temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT huxiao temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT xuwei temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT renyilong temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT zhuxingfei temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT geweihong temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT zhangkunshan temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT liujiping temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT huangrunzhi temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT yujing temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT luodandan temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT yangxuejiao temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT zhuwenmin temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT zhurongrong temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT zhengchanghong temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT sunyieve temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury AT chengliming temporalandspatialcellularandmolecularpathologicalalterationswithsinglecellresolutionintheadultspinalcordafterinjury |