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Metrnl/类Meteorin/IL-41,强直性脊柱炎中骨代谢和疾病活动的新型调节因子:基于多组学分析

Metrnl/Meteorin-like/IL-41, a novel regulator of bone metabolism and disease activity in ankylosing spondylitis: based on multi-omics analysis.

作者信息

Li Zhuoqi, Sun Tao, Zhao Min, Xia Liping, Shen Hui

机构信息

Department of Rheumatology and Immunology, The First Hospital of China Medical University, China Medical University, Shenyang, China.

National Clinical Research Center for Laboratory Medicine, Department of Laboratory Medicine, The First Hospital of China Medical University, Shenyang, China.

出版信息

Front Immunol. 2025 Jul 23;16:1595181. doi: 10.3389/fimmu.2025.1595181. eCollection 2025.

Abstract

BACKGROUND

Ankylosing spondylitis (AS) is an autoimmune disease characterized by bone destruction and abnormal remodeling. Metrnl, a secreted protein involved in inflammation and immune regulation, has recently been linked to bone growth. This study aimed to evaluate serum Metrnl levels in AS patients and explore its bone regulatory mechanisms using cell models and multi-omics analyses.

METHODS

A total of 275 participants aged 16-60 years were included to measure serum Metrnl levels using Enzyme-Linked-Immunosorbent Assay (ELISA). Correlation and receiver operating characteristic (ROC) curve analyses assessed the diagnostic and predictive value of Metrnl. Mouse pre-osteoblastic MC3T3-E1 cells were treated with recombinant Metrnl (0/10/50 ng/mL) during 28-day osteogenic differentiation. RT-qPCR and alkaline phosphatase (ALP)/Alizarin Red S (ARS) staining was used to evaluate direct osteogenic differentiation effects. Transcriptomic and proteomic studies were conducted to further explore bone metabolism mechanisms. Finally, multi-omics integration analyses identified key pathways and targets.

RESULTS

Elevated serum Metrnl levels correlated directly with disease activity markers (CRP, ESR, IL-6) in AS-Active patients, but not in AS-Stable patients. ROC analysis validated Metrnl as a potential auxiliary diagnostic biomarker for high disease activity. , Metrnl suppressed ALP/OCN expression without altering overall osteogenic differentiation. Transcriptomic and proteomic analyses revealed Metrnl's regulatory effects on osteogenic genes and proteins, emphasizing its role in bone and cartilage development. Bioinformatics highlighted Metrnl's inhibition of endochondral ossification, delaying cartilage development and promoting osteoclast differentiation. Multi-omics integration identified Aspn and Sp7 as key targets in bone remodeling and resorption balance.

CONCLUSIONS

Metrnl may serve as an additional diagnostic biomarker for AS and as an indicator for monitoring AS disease activity. Besides, Metrnl plays a critical role in regulating cartilage and bone metabolism and maintaining bone homeostasis, providing new insights for the future diagnosis and treatment of bone-related diseases.

摘要

背景

强直性脊柱炎(AS)是一种以骨质破坏和异常重塑为特征的自身免疫性疾病。Metrnl是一种参与炎症和免疫调节的分泌蛋白,最近与骨骼生长有关。本研究旨在评估AS患者血清Metrnl水平,并使用细胞模型和多组学分析探索其骨调节机制。

方法

共纳入275名年龄在16至60岁之间的参与者,采用酶联免疫吸附测定(ELISA)法检测血清Metrnl水平。相关性分析和受试者工作特征(ROC)曲线分析评估了Metrnl的诊断和预测价值。在小鼠前成骨细胞MC3T3-E1细胞进行28天成骨分化过程中,用重组Metrnl(0/10/50 ng/mL)进行处理。采用RT-qPCR和碱性磷酸酶(ALP)/茜素红S(ARS)染色评估直接成骨分化效果。进行转录组学和蛋白质组学研究以进一步探索骨代谢机制。最后,通过多组学整合分析确定关键途径和靶点。

结果

在活动期AS患者中,血清Metrnl水平升高与疾病活动标志物(CRP、ESR、IL-6)直接相关,但在稳定期AS患者中无此关联。ROC分析验证了Metrnl作为高疾病活动度潜在辅助诊断生物标志物的价值。Metrnl抑制ALP/OCN表达,但不改变整体成骨分化。转录组学和蛋白质组学分析揭示了Metrnl对成骨基因和蛋白质的调节作用,强调了其在骨骼和软骨发育中的作用。生物信息学突出了Metrnl对软骨内骨化的抑制作用,延缓软骨发育并促进破骨细胞分化。多组学整合确定Aspn和Sp7是骨重塑和吸收平衡的关键靶点。

结论

Metrnl可能作为AS的额外诊断生物标志物以及监测AS疾病活动的指标。此外,Metrnl在调节软骨和骨代谢以及维持骨稳态方面起关键作用,为未来骨相关疾病的诊断和治疗提供了新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc4d/12325251/4dcc6f75ada4/fimmu-16-1595181-g001.jpg

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