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PTH(1-34)通过抑制体外 OA 软骨细胞修复中的促炎细胞因子表达,增强骨髓间充质干细胞来源的外泌体的治疗效果。

PTH (1-34) enhances the therapeutic effect of bone marrow mesenchymal stem cell-derived exosomes by inhibiting proinflammatory cytokines expression on OA chondrocyte repair in vitro.

机构信息

Department of Scientific Research Center, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, China.

Department of Critical Care Medicine, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, China.

出版信息

Arthritis Res Ther. 2022 Apr 29;24(1):96. doi: 10.1186/s13075-022-02778-x.

Abstract

BACKGROUND

The effects of bone marrow mesenchymal stem cells (BMSCs) during the treatment of cartilage damage have been proven to be attributed to paracrine mechanisms, particularly the effect of exosomes. Exosomes from different batches are inhomogeneous, and different treatment effects are observed between samples. The purpose of this research was to find more effective and homogeneous exosomes for the repair of chondrocytes in osteoarthritis (OA). We observed the potential effects and possible mechanisms of exosomes derived from parathyroid hormone (PTH) (1-34)-preconditioned BMSCs (Exo) in the alleviation of OA.

MATERIALS AND METHODS

Exosomes derived from BMSCs (Exo) and Exo were isolated by differential centrifugation. Primary rat chondrocytes were used to establish the OA model by interleukin 1 beta (IL-1β) in vitro. The effects of these two types of exosomes on OA chondrocyte proliferation, migration, apoptosis, and extracellular matrix formation were measured and compared. We observed changes in IL-2, TNF-α, and IL-6 levels via Western blotting (WB), and quantitative real-time PCR (qRT-PCR).

RESULTS

We successfully extracted Exo and Exo and established an IL-1β-induced OA model in primary chondrocytes from rats. Our study showed that IL-2, TNF-α, and IL-6 levels increased significantly in OA chondrocytes; however, both Exo and Exo reduced the levels of IL-2, TNF-α, and IL-6. In addition, Exo exhibited stronger anti-inflammatory effects. Exo had a more marked effect on proliferation, migration, and production of the extracellular matrix (Col-II) in OA chondrocytes than Exo at 24 h.

CONCLUSION

Exo increased the migration, proliferation, and chondral matrix formation of OA chondrocytes in vitro. In OA chondrocyte therapy, the potential mechanism of Exo might involve the inhibition of production of proinflammatory cytokines. Although the two types of exosomes had some similar effects, most effects of Exo were better than those of Exo, so Exo may have a better ability to alleviate OA.

摘要

背景

骨髓间充质干细胞(BMSCs)在治疗软骨损伤中的作用已被证明归因于旁分泌机制,特别是外泌体的作用。不同批次的外泌体不均匀,并且在样本之间观察到不同的治疗效果。本研究的目的是寻找更有效和均匀的外泌体,用于修复骨关节炎(OA)中的软骨细胞。我们观察了甲状旁腺激素(PTH)(1-34)预处理的骨髓间充质干细胞(BMSCs)衍生的外泌体(Exo)在缓解 OA 中的潜在作用和可能的机制。

材料和方法

通过差速离心分离 BMSCs 衍生的外泌体(Exo)和 Exo。体外使用白细胞介素 1β(IL-1β)建立原代大鼠软骨细胞 OA 模型。测量并比较了这两种外泌体对 OA 软骨细胞增殖、迁移、凋亡和细胞外基质形成的影响。我们通过 Western blot(WB)和定量实时 PCR(qRT-PCR)观察 IL-2、TNF-α 和 IL-6 水平的变化。

结果

我们成功提取了 Exo 和 Exo,并在大鼠原代软骨细胞中建立了 IL-1β诱导的 OA 模型。我们的研究表明,OA 软骨细胞中的 IL-2、TNF-α 和 IL-6 水平显著升高;然而,Exo 和 Exo 均降低了 IL-2、TNF-α 和 IL-6 的水平。此外,Exo 表现出更强的抗炎作用。与 Exo 相比,Exo 在 24 小时时对 OA 软骨细胞的增殖、迁移和细胞外基质(Col-II)的产生有更明显的作用。

结论

Exo 增加了 OA 软骨细胞在体外的迁移、增殖和软骨基质形成。在 OA 软骨细胞治疗中,Exo 的潜在机制可能涉及抑制促炎细胞因子的产生。虽然两种外泌体具有一些相似的作用,但 Exo 的大多数作用都优于 Exo,因此 Exo 可能具有更好的缓解 OA 的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5ca/9052609/fdc8b5624fff/13075_2022_2778_Fig1_HTML.jpg

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