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Anti-inflammatory effect of hesperidin enhances chondrogenesis of human mesenchymal stem cells for cartilage tissue repair

机译:哈培蛋白的抗炎作用增强了软骨组织修复的人间充质干细胞的软骨发生

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Articular cartilage diseases are considered a major health problem, and tissue engineering using human mesenchymal stem cells (MSCs) have been shown as a promising solution for cartilage tissue repair. Hesperidin is a flavonoid extract from citrus fruits with anti-inflammatory properties. We aimed to investigate the effect of hesperidin on MSCs for cartilage tissue repair. MSCs were treated by hesperidin, and colony formation and proliferation assays were performed to evaluate self-renewal ability of MSCs. Alcian blue staining and Sox9 expression were measured to evaluate chondrogenesis of MSCs. Secretion of pro-inflammatory cytokines IFN-γ, IL-2, IL-4 and IL-10, and expression of nuclear factor kappa B (NF-κB) subunit p65 were also assessed. Hesperidin improved self-renewal ability and chondrogenesis of MSCs, inhibited secretion of pro-inflammatory cytokines IFN-γ, IL-2, IL-4 and IL-10, and suppressed the expression of p65. Overexpression of p65 was able to reverse the hesperidin inhibited secretions of pro-inflammatory cytokines, and abolish the enhancing effect of hesperidin on chondrogenesis of MSCs. Hesperidin could serve as a therapeutic agent to effectively enhance chondrogenesis of human MSCs by inhibiting inflammation to facilitate cartilage tissue repair.
机译:关节软骨疾病被认为是一个主要的健康问题,并且使用人间充质干细胞(MSCs)的组织工程被显示为软骨组织修复的有希望的解决方案。 Hesperidin是一种来自柑橘类水果的黄酮类化合物,具有抗炎性质。我们的旨在探讨Hesperidin对软骨组织修复MSCs的影响。 MSCs被橙皮素治疗,并进行菌落形成和增殖测定以评估MSCs的自我更新能力。测量Alcian蓝染色和SOx9表达,评估MSC的软骨发生。还评估了促炎细胞因子IFN-γ,IL-2,IL-4和IL-10的分泌,以及核因子Kappa B(NF-κB)亚基P65的表达。 Hesperidin改善了MSCs的自我更新能力和软骨发生,抑制了促炎细胞因子IFN-γ,IL-2,IL-4和IL-10的分泌,并抑制了P65的表达。 P65的过度表达能够逆转橙皮蛋白抑制促炎细胞因子的分泌物,并取消了橙皮素对MSC的软骨发生的增强作用。 Hesperidin可以用作治疗剂,通过抑制炎症以促进软骨组织修复来有效地增强人体MSC的软骨菌。

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