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Integrative and comparative single-cell analysis reveals transcriptomic difference between human tumefactive demyelinating lesion and glioma

Tumefactive demyelinating lesion (TDL) is an immune-mediated disease which can be misdiagnosed as glioma. At present, there is no study comparing difference between the two disorders at the cellular level. Here, we perform integrative and comparative single-cell RNA sequencing (ScRNA-seq) transcript...

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Autores principales: Chen, Xiao-Yong, Chen, Yue, Fang, Wen-Hua, Wu, Zan-Yi, Wang, Deng-Liang, Xu, Ya-Wen, Yu, Liang-Hong, Lin, Yuan-Xiang, Kang, De-Zhi, Ding, Chen-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463163/
https://www.ncbi.nlm.nih.gov/pubmed/36085357
http://dx.doi.org/10.1038/s42003-022-03900-0
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author Chen, Xiao-Yong
Chen, Yue
Fang, Wen-Hua
Wu, Zan-Yi
Wang, Deng-Liang
Xu, Ya-Wen
Yu, Liang-Hong
Lin, Yuan-Xiang
Kang, De-Zhi
Ding, Chen-Yu
author_facet Chen, Xiao-Yong
Chen, Yue
Fang, Wen-Hua
Wu, Zan-Yi
Wang, Deng-Liang
Xu, Ya-Wen
Yu, Liang-Hong
Lin, Yuan-Xiang
Kang, De-Zhi
Ding, Chen-Yu
author_sort Chen, Xiao-Yong
collection PubMed
description Tumefactive demyelinating lesion (TDL) is an immune-mediated disease which can be misdiagnosed as glioma. At present, there is no study comparing difference between the two disorders at the cellular level. Here, we perform integrative and comparative single-cell RNA sequencing (ScRNA-seq) transcriptomic analysis on TDL and glioma lesions. At single-cell resolution, TDL is comprised primarily of immune cells, which is completely different from glioma. The integrated analysis reveals a TDL-specific microglial subset involving in B cell activation and proliferation. Comparative analysis highlights remyelination function of glial cells and demyelination function of T cells in TDL. Subclustering and pseudotime trajectory analysis of T cells in TDL reveal their heterogeneity and diverse functions involving in TDL pathogenesis and recovery process. Our study identifies substantial differences between TDL and glioma at single-cell resolution. The observed heterogeneity and potentially diverse functions of cells in TDL may be critical in disease progression.
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spelling pubmed-94631632022-09-11 Integrative and comparative single-cell analysis reveals transcriptomic difference between human tumefactive demyelinating lesion and glioma Chen, Xiao-Yong Chen, Yue Fang, Wen-Hua Wu, Zan-Yi Wang, Deng-Liang Xu, Ya-Wen Yu, Liang-Hong Lin, Yuan-Xiang Kang, De-Zhi Ding, Chen-Yu Commun Biol Article Tumefactive demyelinating lesion (TDL) is an immune-mediated disease which can be misdiagnosed as glioma. At present, there is no study comparing difference between the two disorders at the cellular level. Here, we perform integrative and comparative single-cell RNA sequencing (ScRNA-seq) transcriptomic analysis on TDL and glioma lesions. At single-cell resolution, TDL is comprised primarily of immune cells, which is completely different from glioma. The integrated analysis reveals a TDL-specific microglial subset involving in B cell activation and proliferation. Comparative analysis highlights remyelination function of glial cells and demyelination function of T cells in TDL. Subclustering and pseudotime trajectory analysis of T cells in TDL reveal their heterogeneity and diverse functions involving in TDL pathogenesis and recovery process. Our study identifies substantial differences between TDL and glioma at single-cell resolution. The observed heterogeneity and potentially diverse functions of cells in TDL may be critical in disease progression. Nature Publishing Group UK 2022-09-09 /pmc/articles/PMC9463163/ /pubmed/36085357 http://dx.doi.org/10.1038/s42003-022-03900-0 Text en © The Author(s) 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
Chen, Xiao-Yong
Chen, Yue
Fang, Wen-Hua
Wu, Zan-Yi
Wang, Deng-Liang
Xu, Ya-Wen
Yu, Liang-Hong
Lin, Yuan-Xiang
Kang, De-Zhi
Ding, Chen-Yu
Integrative and comparative single-cell analysis reveals transcriptomic difference between human tumefactive demyelinating lesion and glioma
title Integrative and comparative single-cell analysis reveals transcriptomic difference between human tumefactive demyelinating lesion and glioma
title_full Integrative and comparative single-cell analysis reveals transcriptomic difference between human tumefactive demyelinating lesion and glioma
title_fullStr Integrative and comparative single-cell analysis reveals transcriptomic difference between human tumefactive demyelinating lesion and glioma
title_full_unstemmed Integrative and comparative single-cell analysis reveals transcriptomic difference between human tumefactive demyelinating lesion and glioma
title_short Integrative and comparative single-cell analysis reveals transcriptomic difference between human tumefactive demyelinating lesion and glioma
title_sort integrative and comparative single-cell analysis reveals transcriptomic difference between human tumefactive demyelinating lesion and glioma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463163/
https://www.ncbi.nlm.nih.gov/pubmed/36085357
http://dx.doi.org/10.1038/s42003-022-03900-0
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