牙周炎
细胞
生物
免疫系统
先天免疫系统
免疫学
促炎细胞因子
炎症
细胞生物学
医学
遗传学
内科学
作者
Quinn T. Easter,Bruno Fernandes Matuck,G. B. Stark,Catherine L. Worth,Alexander V. Predeus,Brayon J. Fremin,Khoa Huynh,Vaishnavi Ranganathan,Zhi Ren,Diana Pereira,Brittany Rupp,Theresa Weaver,Kathryn Miller,Paola Pérez,Akira Hasuike,Zhaoxu Chen,Mandy Bush,Xufeng Qu,Janice S. Lee,Scott H. Randell
标识
DOI:10.1038/s41467-024-49037-y
摘要
Periodontitis affects billions of people worldwide. To address relationships of periodontal niche cell types and microbes in periodontitis, we generated an integrated single-cell RNA sequencing (scRNAseq) atlas of human periodontium (34-sample, 105918-cell), including sulcular and junctional keratinocytes (SK/JKs). SK/JKs displayed altered differentiation states and were enriched for effector cytokines in periodontitis. Single-cell metagenomics revealed 37 bacterial species with cell-specific tropism. Fluorescence in situ hybridization detected intracellular 16 S and mRNA signals of multiple species and correlated with SK/JK proinflammatory phenotypes in situ. Cell-cell communication analysis predicted keratinocyte-specific innate and adaptive immune interactions. Highly multiplexed immunofluorescence (33-antibody) revealed peri-epithelial immune foci, with innate cells often spatially constrained around JKs. Spatial phenotyping revealed immunosuppressed JK-microniches and SK-localized tertiary lymphoid structures in periodontitis. Here, we demonstrate impacts on and predicted interactomics of SK and JK cells in health and periodontitis, which requires further investigation to support precision periodontal interventions in states of chronic inflammation.
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