A Single-Cell Atlas of RNA Alternative Splicing in the Glioma-Immune Ecosystem.

Xiao Song, Deanna Tiek, Minghui Lu, Xiaozhou Yu, Runxin Wu, Maya Walker, Qiu He, Derek Sisbarro, Bo Hu, Shi-Yuan Cheng
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Abstract

Single-cell analysis has refined our understanding of cellular heterogeneity in glioma, yet RNA alternative splicing (AS)-a critical layer of transcriptome regulation-remains underexplored at single-cell resolution. Here, we present a pan-glioma single-cell AS analysis in both tumor and immune cells through integrating seven SMART-seq2 datasets of human gliomas. Our analysis reveals lineage-specific AS across glioma cellular states, with the most divergent AS landscapes between mesenchymal- and neuronal-like glioma cells, exemplified by AS in TCF12 and PTBP2 . Comparison between core and peripheral glioma cells highlights AS-redox co-regulation of cytoskeleton organization. Further analysis of glioma-infiltrating immune cells reveals potential isoform-level regulation of protein glycosylation in regulatory T cells and a link between MS4A7 AS in macrophages and clinical response to anti-PD-1 therapy. This study emphasizes the role of AS in glioma cellular heterogeneity, highlighting the importance of an isoform-centric approach to better understand the complex biological processes driving tumorigenesis.

胶质瘤-免疫生态系统中 RNA 替代剪接的单细胞图谱
单细胞分析已经完善了我们对胶质瘤细胞异质性的理解,然而RNA选择性剪接(AS)-转录组调节的关键层-在单细胞分辨率上仍未得到充分探索。在这里,我们通过整合7个人类胶质瘤的SMART-seq2数据集,在肿瘤和免疫细胞中进行泛胶质瘤单细胞AS分析。我们的分析揭示了神经胶质瘤细胞状态的谱系特异性AS,间充质和神经元样胶质瘤细胞之间的AS景观差异最大,例如TCF12和PTBP2中的AS。核心和外周胶质瘤细胞的比较突出了细胞骨架组织的as -氧化还原协同调节。对胶质瘤浸润免疫细胞的进一步分析揭示了调节性T细胞中蛋白糖基化的潜在同型水平调控,以及巨噬细胞中MS4A7 AS与抗pd -1治疗的临床反应之间的联系。这项研究强调了AS在胶质瘤细胞异质性中的作用,强调了以异构体为中心的方法对更好地理解驱动肿瘤发生的复杂生物学过程的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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