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定义口腔炎症性疾病反应中的人类间充质和上皮细胞异质性。

Defining human mesenchymal and epithelial heterogeneity in response to oral inflammatory disease.

机构信息

Centre for Craniofacial and Regenerative Biology, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.

Department of Periodontology, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.

出版信息

Elife. 2021 Jan 4;10:e62810. doi: 10.7554/eLife.62810.

Abstract

Human oral soft tissues provide the first barrier of defence against chronic inflammatory disease and hold a remarkable scarless wounding phenotype. Tissue homeostasis requires coordinated actions of epithelial, mesenchymal, and immune cells. However, the extent of heterogeneity within the human oral mucosa and how tissue cell types are affected during the course of disease progression is unknown. Using single-cell transcriptome profiling we reveal a striking remodelling of the epithelial and mesenchymal niches with a decrease in functional populations that are linked to the aetiology of the disease. Analysis of ligand-receptor interaction pairs identify potential intercellular hubs driving the inflammatory component of the disease. Our work establishes a reference map of the human oral mucosa in health and disease, and a framework for the development of new therapeutic strategies.

摘要

人类口腔软组织是抵御慢性炎症性疾病的第一道防线,具有显著的无瘢痕创伤表型。组织稳态需要上皮细胞、间充质细胞和免疫细胞的协调作用。然而,目前尚不清楚人类口腔黏膜内的异质性程度以及在疾病进展过程中组织细胞类型受到的影响。通过单细胞转录组谱分析,我们揭示了上皮和间充质生态位的显著重构,与疾病病因相关的功能群体减少。配体-受体相互作用对的分析确定了潜在的细胞间枢纽,这些枢纽驱动着疾病的炎症成分。我们的工作为人类口腔黏膜的健康和疾病建立了一个参考图谱,并为新的治疗策略的发展提供了一个框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efd8/7781605/83009c6fb104/elife-62810-fig1.jpg

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