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Therapeutic effect of mesenchymal stem cells derived from human umbilical cord in rabbit temporomandibular joint model of osteoarthritis

机译:间充质干细胞源性脐带中的间充质干细胞在腹腔炎颞下颌关节模型中衍生自脐带

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Osteoarthritis (OA) is a degenerative condition of the temporomandibular joint (TMJ) characterised by chronic inflammation and damage to joint structures. Because of the complexity of TMJ-OA, only symptomatic treatments are currently available. Recent reports have shown that many of stem cells can exert anti-inflammatory and tissue-regenerating effects. In this study, we investigated the potential cartilage-regenerating and anti-inflammatory effects of human umbilical cord matrix-mesenchymal stem cells (hUCM-MSCs) for the treatment of TMJ-OA. hUCM-MSC lines, isolated from different donors, which showed different activities in vitro. Using a selected cell line, we used different concentrations of hUCM-MSCs to assess therapeutic effects in a rabbit model of monosodium iodoacetate-induced TMJ-OA. Compared with the untreated control group, the potential regenerative result and anti-inflammatory effects of hUCM-MSCs were evident at all the tested concentrations in rabbits with induced TMJ-OA. The median dose of hUCM-MSCs showed the prominent cartilage protective effect and further cartilage regeneration potential. This effect occurred via upregulated expression of growth factors, extracellular matrix markers, and anti-inflammatory cytokines, and reduced expression of pro-inflammatory cytokines. The anti-inflammatory effect of hUCM-MSCs was comparable to that of dexamethasone (DEX). However, only hUCM-MSCs showed potential chondrogenesis effects in this study. In conclusion, our results indicate that hUCM-MSCs may be an effective treatment option for the treatment of TMJ-OA.
机译:骨关节炎(OA)是颞下颌关节(TMJ)的退行性条件,其特征在于慢性炎症和关节结构的损伤。由于TMJ-OA的复杂性,目前只有对症治疗。最近的报道表明,许多干细胞可以发挥抗炎和组织再生效果。在这项研究中,我们研究了人脐脊髓基质 - 间充质干细胞(HUCM-MSC)治疗TMJ-OA的潜在软骨再生和抗炎作用。 HUCM-MSC线路,来自不同供体的线,在体外显示出不同的活性。使用选定的细胞系,我们使用不同浓度的HUCM-MSCs来评估碘碘酸钠诱导的TMJ-OA的兔模型中的治疗效果。与未处理的对照组相比,HUCM-MSCs的潜在再生结果和抗炎作用在具有诱导的TMJ-OA的兔子中的所有测试浓度下是显而易见的。 HUCM-MSCs的中值剂量显示出突出的软骨保护效果和进一步的软骨再生电位。这种效果通过增长因子,细胞外基质标记和抗炎细胞因子的上调表达,以及减少促炎细胞因子的表达。 HUCM-MSCs的抗炎作用与地塞米松(DEX)的抗炎作用相当。然而,只有HUCM-MSCs在这项研究中显示出潜在的软骨发生效应。总之,我们的结果表明HUCM-MSCs可以是治疗TMJ-OA的有效治疗选择。

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