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绘制人类星形胶质细胞的发育轨迹揭示了胶质母细胞瘤中的差异。

Mapping the developmental trajectory of human astrocytes reveals divergence in glioblastoma.

作者信息

Sojka Caitlin, Wang Hsiao-Lin V, Bhatia Tarun N, Li Yangping, Chopra Pankaj, Sing Anson, Voss Anna, King Alexia, Wang Feng, Joseph Kevin, Ravi Vidhya M, Olson Jeffrey, Hoang Kimberly, Nduom Edjah, Corces Victor G, Yao Bing, Sloan Steven A

机构信息

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.

Emory Center for Neurodegenerative Disease, Emory University School of Medicine, Atlanta, GA, USA.

出版信息

Nat Cell Biol. 2025 Feb;27(2):347-359. doi: 10.1038/s41556-024-01583-9. Epub 2025 Jan 8.

Abstract

Glioblastoma (GBM) is defined by heterogeneous and resilient cell populations that closely reflect neurodevelopmental cell types. Although it is clear that GBM echoes early and immature cell states, identifying the specific developmental programmes disrupted in these tumours has been hindered by a lack of high-resolution trajectories of glial and neuronal lineages. Here we delineate the course of human astrocyte maturation to uncover discrete developmental stages and attributes mirrored by GBM. We generated a transcriptomic and epigenomic map of human astrocyte maturation using cortical organoids maintained in culture for nearly 2 years. Through this approach, we chronicled a multiphase developmental process. Our time course of human astrocyte maturation includes a molecularly distinct intermediate period that serves as a lineage commitment checkpoint upstream of mature quiescence. This intermediate stage acts as a site of developmental deviation separating IDH-wild-type neoplastic astrocyte-lineage cells from quiescent astrocyte populations. Interestingly, IDH1-mutant tumour astrocyte-lineage cells are the exception to this developmental perturbation, where immature properties are suppressed as a result of D-2-hydroxyglutarate oncometabolite exposure. We propose that this defiance is a consequence of IDH1-mutant-associated epigenetic dysregulation, and we identified biased DNA hydroxymethylation (5hmC) in maturation genes as a possible mechanism. Together, this study illustrates a distinct cellular state aberration in GBM astrocyte-lineage cells and presents developmental targets for experimental and therapeutic exploration.

摘要

胶质母细胞瘤(GBM)由异质性且具有韧性的细胞群体所定义,这些细胞群体与神经发育细胞类型密切相关。尽管很明显GBM反映了早期和未成熟的细胞状态,但由于缺乏神经胶质和神经元谱系的高分辨率轨迹,确定这些肿瘤中被破坏的特定发育程序一直受到阻碍。在这里,我们描绘了人类星形胶质细胞成熟的过程,以揭示GBM所反映的离散发育阶段和特征。我们使用在培养中维持了近2年的皮质类器官生成了人类星形胶质细胞成熟的转录组和表观基因组图谱。通过这种方法,我们记录了一个多阶段的发育过程。我们的人类星形胶质细胞成熟时间进程包括一个分子上不同的中间期,它作为成熟静止上游的谱系承诺检查点。这个中间阶段充当了一个发育偏差位点,将异柠檬酸脱氢酶(IDH)野生型肿瘤性星形胶质细胞谱系细胞与静止的星形胶质细胞群体分开。有趣的是,IDH1突变的肿瘤星形胶质细胞谱系细胞是这种发育扰动的例外,由于暴露于D-2-羟基戊二酸肿瘤代谢物,其未成熟特性受到抑制。我们认为这种抗性是IDH1突变相关的表观遗传失调的结果,并且我们确定成熟基因中的偏向性DNA羟甲基化(5hmC)是一种可能的机制。总之,这项研究阐明了GBM星形胶质细胞谱系细胞中一种独特的细胞状态异常,并为实验和治疗探索提供了发育靶点。

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