AI Article Synopsis

  • - The study investigates Tumefactive Demyelinating Lesions (TDL) and glioma, which can be confused for each other, using single-cell RNA sequencing to analyze the differences at a cellular level.
  • - Findings show that TDL primarily consists of immune cells, unlike glioma, and includes a unique microglial subset that activates and proliferates B cells.
  • - The research highlights TDL's complex T cell functions related to both demyelination and recovery, emphasizing significant differences in cell types and functions that could impact disease progression.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463163PMC
http://dx.doi.org/10.1038/s42003-022-03900-0DOI Listing

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