在体内大鼠模型中,关节内注射血小板裂解物衍生的细胞外囊泡可改善膝骨关节炎。

Intra-articular injection of platelet lysate-derived extracellular vesicles recovers from knee osteoarthritis in an in vivo rat model.

作者信息

Forteza-Genestra Maria Antònia, Antich-Rosselló Miquel, Ráez-Meseguer Carmen, Sangenís Anna Tomàs, Calvo Javier, Gayà Antoni, Monjo Marta, Ramis Joana Maria

机构信息

Cell Therapy and Tissue Engineering Group, Research Institute on Health Sciences (IUNICS), University of the Balearic Islands, Crta Valldemossa km 7.5, 07122, Palma, Spain.

Health Research Institute of the Balearic Islands (IdISBa), 07120, Palma, Spain.

出版信息

J Orthop Translat. 2024 Feb 8;45:1-9. doi: 10.1016/j.jot.2023.10.005. eCollection 2024 Mar.

Abstract

OBJECTIVE

MSCs and Platelet-Rich Plasma are the main focus in the study of new regenerative treatments aimed to reverse Osteoarthritis (OA). However, extracellular vesicles (EVs) present several advantages to cell-based treatments. Thus, the aim of this study was to compare and evaluate the regenerative potential of MSC-derived EVs (cEVs) and platelet-derived EVs (pEVs) in an OA cartilage rat model.

DESIGN

OA in vivo model was established through injection of 6 mg MIA in the rat knee joints. After 14 and 21 days, OA knee joints were treated with 1 × 10 particles of pEVs or cEVs. At day 28, the animals were sacrificed, plasma was collected to quantify CTX-II and knee joints were excised to be evaluated by Cone Beam Computed Tomography (CBCT). After decalcification, histology was used to determine the OARSI score and to visualize collagen and glycosaminoglycan content.

RESULTS

pEVs and cEVs samples did not show significant differences per se but they did in terms of regenerative effects on OA knee joints. pEVs-treated knee joints showed better subchondral bone integrity in CT-analysed parameters when compared to cEVs or OA group, showing similar values to the healthy control group. Moreover, OARSI score indicated that pEVs showed a greater OA reversion in knee joints, especially in female rats, and so indicated the analysed histological images.

CONCLUSIONS

pEVs are proposed as a viable regeneration treatment for OA since they are not only capable of exerting their regenerative potential on osteoarthritic cartilage, but also outperform cEVs in terms of efficacy, particularly in females.

SIGNIFICANCE STATEMENT

Osteoarthritis (OA) is one of the most age-related diseases. It is estimated that 500 million people suffer from OA worldwide, representing the principal cause of chronic disability in adults. In the present study we evaluated the therapeutic effect of extracellular vesicles (EVs) from different sources (platelet lysate and human umbilical cord mesenchymal stromal cells) in an in vivo rat model. Our results demonstrate that platelet-derived EVs (pEVs) induce an OA reversion in knee joints, thus evidencing the therapeutic potential of pEVs as cell-free regenerative agents for OA treatment.

THE TRANSLATIONAL POTENTIAL OF THIS ARTICLE

Platelet-derived extracellular vesicles (pEVs) offer a promising cell-free therapy option for OA treatment. Their production could be easily standardized and reproduced without extensive platelet harvesting and amplification, thus paving the way for their clinical translation.

摘要

目的

间充质干细胞(MSCs)和富血小板血浆是旨在逆转骨关节炎(OA)的新型再生治疗研究的主要焦点。然而,细胞外囊泡(EVs)在基于细胞的治疗中具有若干优势。因此,本研究的目的是在OA软骨大鼠模型中比较和评估间充质干细胞来源的细胞外囊泡(cEVs)和血小板来源的细胞外囊泡(pEVs)的再生潜力。

设计

通过向大鼠膝关节注射6mg单碘乙酸(MIA)建立OA体内模型。在14天和21天后,用1×10个pEVs或cEVs颗粒治疗OA膝关节。在第28天,处死动物,收集血浆以定量Ⅱ型胶原C-末端肽(CTX-II),并切除膝关节以通过锥形束计算机断层扫描(CBCT)进行评估。脱钙后,采用组织学方法确定骨关节炎研究学会国际工作组(OARSI)评分,并观察胶原和糖胺聚糖含量。

结果

pEVs和cEVs样本本身未显示出显著差异,但它们对OA膝关节的再生效果存在差异。与cEVs或OA组相比,pEVs治疗的膝关节在CT分析参数中显示出更好的软骨下骨完整性,与健康对照组的值相似。此外,OARSI评分表明,pEVs在膝关节中显示出更大的OA逆转,尤其是在雌性大鼠中,分析的组织学图像也表明了这一点。

结论

pEVs被认为是一种可行的OA再生治疗方法,因为它们不仅能够在骨关节炎软骨上发挥其再生潜力,而且在疗效方面优于cEVs,尤其是在雌性中。

意义声明

骨关节炎(OA)是最常见的与年龄相关的疾病之一。据估计,全球有5亿人患有OA,是成年人慢性残疾的主要原因。在本研究中,我们在体内大鼠模型中评估了来自不同来源(血小板裂解物和人脐带间充质基质细胞)的细胞外囊泡(EVs)的治疗效果。我们的结果表明,血小板来源的细胞外囊泡(pEVs)可诱导膝关节OA逆转,从而证明pEVs作为OA治疗的无细胞再生剂的治疗潜力。

本文的转化潜力

血小板来源的细胞外囊泡(pEVs)为OA治疗提供了一种有前景的无细胞治疗选择。它们的生产可以很容易地标准化和复制,而无需大量采集和扩增血小板,从而为其临床转化铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7129/10873568/91868f29cfa4/ga1.jpg

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