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Single-cell RNA sequencing analysis of vestibular schwannoma reveals functionally distinct macrophage subsets.

Baruah, P; Mahony, C; Marshall, JL; Smith, CG; Monksfield, P; Irving, RI; Dumitriu, IE; Buckley, CD; Croft, AP (2024) Single-cell RNA sequencing analysis of vestibular schwannoma reveals functionally distinct macrophage subsets. Br J Cancer, 130 (10). pp. 1659-1669. ISSN 1532-1827 https://doi.org/10.1038/s41416-024-02646-2
SGUL Authors: Dumitriu, Ingrid Elena

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Abstract

BACKGROUND: Vestibular schwannomas (VSs) remain a challenge due to their anatomical location and propensity to growth. Macrophages are present in VS but their roles in VS pathogenesis remains unknown. OBJECTIVES: The objective was to assess phenotypic and functional profile of macrophages in VS with single-cell RNA sequencing (scRNAseq). METHODS: scRNAseq was carried out in three VS samples to examine characteristics of macrophages in the tumour. RT-qPCR was carried out on 10 VS samples for CD14, CD68 and CD163 and a panel of macrophage-associated molecules. RESULTS: scRNAseq revealed macrophages to be a major constituent of VS microenvironment with three distinct subclusters based on gene expression. The subclusters were also defined by expression of CD163, CD68 and IL-1β. AREG and PLAUR were expressed in the CD68+CD163+IL-1β+ subcluster, PLCG2 and NCKAP5 were expressed in CD68+CD163+IL-1β- subcluster and AUTS2 and SPP1 were expressed in the CD68+CD163-IL-1β+ subcluster. RT-qPCR showed expression of several macrophage markers in VS of which CD14, ALOX15, Interleukin-1β, INHBA and Colony Stimulating Factor-1R were found to have a high correlation with tumour volume. CONCLUSIONS: Macrophages form an important component of VS stroma. scRNAseq reveals three distinct subsets of macrophages in the VS tissue which may have differing roles in the pathogenesis of VS.

Item Type: Article
Additional Information: © The Author(s) 2024 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
Keywords: 1112 Oncology and Carcinogenesis, 1117 Public Health and Health Services, Oncology & Carcinogenesis
Journal or Publication Title: Br J Cancer
ISSN: 1532-1827
Language: eng
Dates:
DateEvent
1 June 2024Published
13 March 2024Published Online
27 February 2024Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
RCSgrant2021Royal College of Surgeons of Englandhttp://dx.doi.org/10.13039/501100000297
20298Versus Arthritishttp://dx.doi.org/10.13039/501100012041
19791Versus Arthritishttp://dx.doi.org/10.13039/501100012041
PubMed ID: 38480935
Web of Science ID: WOS:001184586600002
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116447
Publisher's version: https://doi.org/10.1038/s41416-024-02646-2

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