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间充质干细胞衍生的细胞外囊泡作为一种潜在的更有益的治疗策略,优于基于 MSC 的治疗方法,可用于轻度代谢性骨关节炎模型。

Mesenchymal stem/stromal cells-derived extracellular vesicles as a potentially more beneficial therapeutic strategy than MSC-based treatment in a mild metabolic osteoarthritis model.

机构信息

Regenerative Medicine Center, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.

Department of Orthopedics, University Medical Center Utrecht, PO Box 85500, 3508 GA, Utrecht, The Netherlands.

出版信息

Stem Cell Res Ther. 2023 May 24;14(1):137. doi: 10.1186/s13287-023-03368-7.


DOI:10.1186/s13287-023-03368-7
PMID:37226203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10210425/
Abstract

BACKGROUND: Mesenchymal stromal/stem cells (MSCs) and MSC-derived extracellular vesicles (MSC-EVs) hold promise as a disease modifying treatment in osteoarthritis (OA). Obesity, and its associated inflammation, contribute to OA development and metabolic OA represents a specific and significant group of the OA patient population. Given their immunomodulatory properties, MSC and MSC-EVs are especially interesting for this group of patients as a therapeutic option. Here, we were the first to compare the therapeutic efficacy of MSCs and MSC-EVs in a mild OA model taking these metabolic aspects into consideration. METHODS: Male Wistar-Han rats (Crl:WI(Han) (n = 36) were fed a high fat diet for 24 weeks, with unilateral induction of OA by groove surgery after 12 weeks. Eight days after surgery rats were randomized in three treatment groups receiving MSCs, MSC-EVs or vehicle injection. Pain-associated behavior, joint degeneration, and local and systemic inflammation were measured. RESULTS: We demonstrated that despite not having a significant therapeutic effect, MSC-EV treatment results in lower cartilage degeneration, less pain behaviour, osteophytosis and joint inflammation, than MSC treatment. Suggesting that MSC-EVs could be a more promising therapeutic strategy than MSCs in this mild metabolic OA model. CONCLUSION: In summary, we find that MSC treatment has negative effects on the joint in metabolic mild OA. This is an essential finding for the significant group of patients with metabolic OA phenotype, and might help to understand why clinical translation of MSC treatment shows varying therapeutic efficacy thus far. Our results also suggest that MSC-EV-based treatment might be a promising option for these patients, however MSC-EV therapeutic efficacy will need improvement.

摘要

背景:间充质基质/干细胞(MSCs)和 MSC 衍生的细胞外囊泡(MSC-EVs)有望成为骨关节炎(OA)的疾病修饰治疗方法。肥胖及其相关炎症会导致 OA 的发展,代谢性 OA 代表了 OA 患者人群中的一个特定和重要群体。鉴于它们的免疫调节特性,MSC 和 MSC-EVs 作为一种治疗选择,对这群患者特别有吸引力。在这里,我们首次在考虑这些代谢因素的情况下,在轻度 OA 模型中比较了 MSCs 和 MSC-EVs 的治疗效果。

方法:雄性 Wistar-Han 大鼠(Crl:WI(Han)(n=36)接受高脂肪饮食喂养 24 周,12 周后单侧沟手术诱导 OA。手术后 8 天,大鼠随机分为三组,分别接受 MSC、MSC-EV 或载体注射治疗。测量疼痛相关行为、关节退变以及局部和全身炎症。

结果:我们证明,尽管 MSC-EV 治疗没有显著的治疗效果,但与 MSC 治疗相比,MSC-EV 治疗导致软骨退变、疼痛行为、骨赘形成和关节炎症减少。这表明,在这种轻度代谢性 OA 模型中,MSC-EVs 可能是一种比 MSC 更有前途的治疗策略。

结论:综上所述,我们发现 MSC 治疗对代谢性轻度 OA 关节有负面影响。这对于代谢性 OA 表型的患者群体来说是一个重要的发现,并且可能有助于解释为什么迄今为止 MSC 治疗的临床转化显示出不同的治疗效果。我们的结果还表明,基于 MSC-EV 的治疗可能是这些患者的一种有前途的选择,然而 MSC-EV 的治疗效果仍需改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8373/10210425/f8f43bb1226d/13287_2023_3368_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8373/10210425/d4ca3b23fd73/13287_2023_3368_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8373/10210425/2ca1cf4bf4d8/13287_2023_3368_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8373/10210425/805e84768a1b/13287_2023_3368_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8373/10210425/f8f43bb1226d/13287_2023_3368_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8373/10210425/d4ca3b23fd73/13287_2023_3368_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8373/10210425/2ca1cf4bf4d8/13287_2023_3368_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8373/10210425/805e84768a1b/13287_2023_3368_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8373/10210425/f8f43bb1226d/13287_2023_3368_Fig4_HTML.jpg

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[5]
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[6]
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[7]
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[8]
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[9]
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本文引用的文献

[1]
Pharmacokinetics, safety and efficacy of intra-articular non-steroidal anti-inflammatory drug injections for the treatment of osteoarthritis: A narrative review.

J Clin Pharm Ther. 2022-8

[2]
Sprague Dawley Rats Show More Severe Bone Loss, Osteophytosis and Inflammation Compared toWistar Han Rats in a High-Fat, High-Sucrose Diet Model of Joint Damage.

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LncRNA Malat-1 From MSCs-Derived Extracellular Vesicles Suppresses Inflammation and Cartilage Degradation in Osteoarthritis.

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Acta Biomater. 2021-3-1

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Exosomes derived from miR-155-5p-overexpressing synovial mesenchymal stem cells prevent osteoarthritis via enhancing proliferation and migration, attenuating apoptosis, and modulating extracellular matrix secretion in chondrocytes.

Cell Biol Toxicol. 2021-2

[10]
Metabolic syndrome increases senescence-associated micro-RNAs in extracellular vesicles derived from swine and human mesenchymal stem/stromal cells.

Cell Commun Signal. 2020-8-12

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