转运蛋白(18kDA)(TSPO)标记间充质胶质母细胞瘤细胞群,其特征是肿瘤相关巨噬细胞数量增加。

IF 6.2 2区 医学 Q1 NEUROSCIENCES
Lorraine Weidner, Julia Lorenz, Stefanie Quach, Frank K Braun, Tanja Rothhammer-Hampl, Laura-Marie Ammer, Arabel Vollmann-Zwerenz, Laura M Bartos, Franziska J Dekorsy, Adrien Holzgreve, Sabrina V Kirchleitner, Niklas Thon, Tobias Greve, Viktoria Ruf, Jochen Herms, Stefanie Bader, Vladimir M Milenkovic, Louisa von Baumgarten, Ayse N Menevse, Abir Hussein, Julian Sax, Christian H Wetzel, Rainer Rupprecht, Martin Proescholdt, Nils O Schmidt, Philipp Beckhove, Peter Hau, Joerg-Christian Tonn, Peter Bartenstein, Matthias Brendel, Nathalie L Albert, Markus J Riemenschneider
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引用次数: 0

摘要

TSPO是一种很有前途的新型脑肿瘤正电子发射断层扫描(PET)示踪靶点。然而,由于有助于TSPO-PET信号的细胞群体的异质性,成像解释可能具有挑战性。因此,我们评估了TSPO在胶质瘤中的富集/表达及其潜在的组织病理学和分子特征。我们在大型计算机数据集中分析了TSPO的表达及其调控机制,并对TSPO启动子进行了直接亚硫酸氢盐测序。在我们的TSPO-PET成像研究队列的胶质母细胞瘤组织样本中,我们通过免疫组织化学和荧光多重染色分析了TSPO示踪剂富集和蛋白质标记与细胞谱系标记物表达的关系。此外,我们通过RNA测序确定了相关的TSPO相关信号通路。我们发现TSPO的表达与预后不良的神经胶质瘤表型有关,TSPO启动子高甲基化与IDH突变有关。仔细的组织学分析显示,TSPO免疫组织化学与TSPO-PET信号相关,TSPO在不同的细胞群体中表达。虽然肿瘤核心区域是总TSPO信号的主要贡献者,但肿瘤边缘的TSPO信号主要由CD68阳性的小胶质细胞/巨噬细胞驱动。TSPO的高表达标志着预后不良的胶质母细胞瘤细胞亚群,其特征是间充质基因集富集和肿瘤相关巨噬细胞数量增加。总之,我们的研究通过揭示TSPO表达/调节的IDH依赖性差异、TSPO PET信号的区域异质性以及TSPO在肿瘤免疫细胞相互作用方面的功能意义,提高了对TSPO作为胶质瘤成像标志物的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Translocator protein (18kDA) (TSPO) marks mesenchymal glioblastoma cell populations characterized by elevated numbers of tumor-associated macrophages.

Translocator protein (18kDA) (TSPO) marks mesenchymal glioblastoma cell populations characterized by elevated numbers of tumor-associated macrophages.

Translocator protein (18kDA) (TSPO) marks mesenchymal glioblastoma cell populations characterized by elevated numbers of tumor-associated macrophages.

Translocator protein (18kDA) (TSPO) marks mesenchymal glioblastoma cell populations characterized by elevated numbers of tumor-associated macrophages.

TSPO is a promising novel tracer target for positron-emission tomography (PET) imaging of brain tumors. However, due to the heterogeneity of cell populations that contribute to the TSPO-PET signal, imaging interpretation may be challenging. We therefore evaluated TSPO enrichment/expression in connection with its underlying histopathological and molecular features in gliomas. We analyzed TSPO expression and its regulatory mechanisms in large in silico datasets and by performing direct bisulfite sequencing of the TSPO promotor. In glioblastoma tissue samples of our TSPO-PET imaging study cohort, we dissected the association of TSPO tracer enrichment and protein labeling with the expression of cell lineage markers by immunohistochemistry and fluorescence multiplex stains. Furthermore, we identified relevant TSPO-associated signaling pathways by RNA sequencing.We found that TSPO expression is associated with prognostically unfavorable glioma phenotypes and that TSPO promotor hypermethylation is linked to IDH mutation. Careful histological analysis revealed that TSPO immunohistochemistry correlates with the TSPO-PET signal and that TSPO is expressed by diverse cell populations. While tumor core areas are the major contributor to the overall TSPO signal, TSPO signals in the tumor rim are mainly driven by CD68-positive microglia/macrophages. Molecularly, high TSPO expression marks prognostically unfavorable glioblastoma cell subpopulations characterized by an enrichment of mesenchymal gene sets and higher amounts of tumor-associated macrophages.In conclusion, our study improves the understanding of TSPO as an imaging marker in gliomas by unveiling IDH-dependent differences in TSPO expression/regulation, regional heterogeneity of the TSPO PET signal and functional implications of TSPO in terms of tumor immune cell interactions.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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