Molecular Determinants of Neutrophil Extracellular Vesicles That Drive Cartilage Regeneration in Inflammatory Arthritis.

IF 11.4 1区 医学 Q1 RHEUMATOLOGY
Bethan L Thomas, Trinidad Montero-Melendez, Silvia Oggero, Magdalena K Kaneva, David Chambers, Andreia L Pinto, Alessandra Nerviani, Davide Lucchesi, Shani Austin-Williams, Mohammed T Hussain, Costantino Pitzalis, Benjamin Allen, Marzia Malcangio, Francesco Dell'Accio, Lucy V Norling, Mauro Perretti
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Abstract

Objective: This study was undertaken to establish the potential therapeutic profile of neutrophil-derived extracellular vesicles (EVs) in experimental inflammatory arthritis and associate pharmacological activity with specific EV components, focusing on microRNAs.

Methods: Neutrophil EVs were administered intra-articularly through a prophylactic or therapeutic protocol to male C57BL/6 mice undergoing serum-transfer-induced inflammatory arthritis. Transcriptomic analysis of knees was performed on joints following EV administration, naive and arthritic mice (untreated; n = 4/group) and EV-treated diseased mice (intra-articular administration) with contralateral (vehicle-treated; n = 8/group). Comparison of healthy donor and patients with rheumatoid arthritis (RA) neutrophil EVs was performed.

Results: EVs afforded cartilage protection with an increase in collagen-II and reduced collagen-X expression within the joint. To gain mechanistic insights, RNA sequencing of the arthritic joints was conducted. A total of 5,231 genes were differentially expressed (P < 0.05), with 257 unique to EV treatment. EVs affected key regenerative pathways involved in joint development, including Wnt and Notch signaling. This wealth of genomic alteration prompted to identify microRNAs in EVs, 10 of which are associated with RA. As a proof of concept, we focused on miR-455-3p, which was detected in both healthy donor and RA EVs. EV addition to chondrocyte cultures elevated miR-455-3p and exerted anticatabolic effects upon interleukin-1β stimulation; these effects were blocked by actinomycin or miR-455-3p antagomir.

Conclusion: Neutrophils from patients with RA yielded EVs with composition, efficacy, and miR-455-3p content similar to those of healthy volunteers, suggesting that neutrophil EVs could be developed as an autologous treatment to protect and repair joint tissue of patients affected by inflammatory arthritides.

Abstract Image

中性粒细胞胞外囊泡的分子决定因素推动炎症性关节炎的软骨再生。
研究目的本研究旨在确定中性粒细胞衍生的细胞外囊泡(EVs)在实验性炎症性关节炎中的潜在治疗特征,并将药理活性与特定的EVs成分联系起来,重点关注microRNAs:方法:通过预防性或治疗性方案,给接受血清转移诱导的炎症性关节炎的雄性 C57BL/6 小鼠关节内注射中性粒细胞囊泡。对给予 EV 后的关节进行膝关节转录组学分析,未接受治疗的小鼠和关节炎小鼠 n=4/组,EV 治疗的患病小鼠(关节内给药)和对侧(药物治疗)n=8/组。对健康供体和类风湿性关节炎(RA)患者的中性粒细胞EV进行了比较:结果:EVs 保护了软骨,增加了关节内胶原蛋白-II 的表达,减少了胶原蛋白-X 的表达。为了深入了解机理,对关节炎关节进行了 RNA 测序。共有 5,231 个基因有差异表达(PConclusion:来自RA患者的中性粒细胞产生的EVs,其成分、功效和miR-455-3p含量与健康志愿者的相似,这表明中性粒细胞EVs可作为一种自体疗法来保护和修复受炎症性关节炎影响的患者的关节组织。
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来源期刊
Arthritis & Rheumatology
Arthritis & Rheumatology RHEUMATOLOGY-
CiteScore
20.90
自引率
3.00%
发文量
371
期刊介绍: Arthritis & Rheumatology is the official journal of the American College of Rheumatology and focuses on the natural history, pathophysiology, treatment, and outcome of rheumatic diseases. It is a peer-reviewed publication that aims to provide the highest quality basic and clinical research in this field. The journal covers a wide range of investigative areas and also includes review articles, editorials, and educational material for researchers and clinicians. Being recognized as a leading research journal in rheumatology, Arthritis & Rheumatology serves the global community of rheumatology investigators and clinicians.
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