单细胞RNA测序和基于人群的研究相结合揭示了手部骨关节炎相关软骨细胞亚群和途径。

IF 14.3 1区 医学 Q1 CELL & TISSUE ENGINEERING Bone Research Pub Date : 2023-11-02 DOI:10.1038/s41413-023-00292-7
Hui Li, Xiaofeng Jiang, Yongbing Xiao, Yuqing Zhang, Weiya Zhang, Michael Doherty, Jacquelyn Nestor, Changjun Li, Jing Ye, Tingting Sha, Houchen Lyu, Jie Wei, Chao Zeng, Guanghua Lei
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引用次数: 0

摘要

手骨关节炎是一种常见的异质性关节疾病,其分子机制尚不清楚,也没有治疗疾病的药物。在这项研究中,我们进行了单细胞RNA测序分析,以比较宏观证实的骨关节炎软骨(n = 5) 无骨关节炎的软骨(n = 5) 来自五个供体的指间关节。共105个 142个细胞,我们鉴定了13个亚群,包括一个具有炎症调节潜力的新亚群,注释为炎症软骨细胞。与非骨性关节炎软骨相比,纤维软骨细胞在骨关节炎软骨中表现出广泛的基因表达模式改变。炎性软骨细胞和纤维软骨细胞在骨关节炎软骨中都显示出数量增加的趋势。在这两个来自骨关节炎软骨的亚群中,脱铁途径富集,铁过载相关基因(如FTH1)的表达升高。为了验证这些发现,我们使用英国生物库进行了一项孟德尔随机化研究,并使用湘雅骨关节炎研究收集的数据进行了一次基于人群的横断面研究。FTH1 mRNA高表达的遗传倾向显著增加了患手部骨关节炎的风险(比值比 = 1.07,95%置信区间:1.02-1.11) = 332 668)在英国生物银行。高水平的血清铁蛋白(由FTH1编码)是身体铁过载的生物标志物,与参与者中手部骨关节炎的高患病率显著相关(n = 1. 241)的湘雅骨关节炎研究(P为趋势 = 0.037)。总之,我们的研究结果表明,炎性软骨细胞和纤维软骨软骨细胞是关键的亚群,脱铁症可能是手部骨关节炎的关键途径,为手部骨骨头炎的病理生理学和潜在的治疗靶点提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Combining single-cell RNA sequencing and population-based studies reveals hand osteoarthritis-associated chondrocyte subpopulations and pathways.

Hand osteoarthritis is a common heterogeneous joint disorder with unclear molecular mechanisms and no disease-modifying drugs. In this study, we performed single-cell RNA sequencing analysis to compare the cellular composition and subpopulation-specific gene expression between cartilage with macroscopically confirmed osteoarthritis (n = 5) and cartilage without osteoarthritis (n = 5) from the interphalangeal joints of five donors. Of 105 142 cells, we identified 13 subpopulations, including a novel subpopulation with inflammation-modulating potential annotated as inflammatory chondrocytes. Fibrocartilage chondrocytes exhibited extensive alteration of gene expression patterns in osteoarthritic cartilage compared with nonosteoarthritic cartilage. Both inflammatory chondrocytes and fibrocartilage chondrocytes showed a trend toward increased numbers in osteoarthritic cartilage. In these two subpopulations from osteoarthritic cartilage, the ferroptosis pathway was enriched, and expression of iron overload-related genes, e.g., FTH1, was elevated. To verify these findings, we conducted a Mendelian randomization study using UK Biobank and a population-based cross-sectional study using data collected from Xiangya Osteoarthritis Study. Genetic predisposition toward higher expression of FTH1 mRNA significantly increased the risk of hand osteoarthritis (odds ratio = 1.07, 95% confidence interval: 1.02-1.11) among participants (n = 332 668) in UK Biobank. High levels of serum ferritin (encoded by FTH1), a biomarker of body iron overload, were significantly associated with a high prevalence of hand osteoarthritis among participants (n = 1 241) of Xiangya Osteoarthritis Study (P-for-trend = 0.037). In conclusion, our findings indicate that inflammatory and fibrocartilage chondrocytes are key subpopulations and that ferroptosis may be a key pathway in hand osteoarthritis, providing new insights into the pathophysiology and potential therapeutic targets of hand osteoarthritis.

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来源期刊
Bone Research
Bone Research CELL & TISSUE ENGINEERING-
CiteScore
20.00
自引率
4.70%
发文量
289
审稿时长
20 weeks
期刊介绍: Established in 2013, Bone Research is a newly-founded English-language periodical that centers on the basic and clinical facets of bone biology, pathophysiology, and regeneration. It is dedicated to championing key findings emerging from both basic investigations and clinical research concerning bone-related topics. The journal's objective is to globally disseminate research in bone-related physiology, pathology, diseases, and treatment, contributing to the advancement of knowledge in this field.
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