Department of Spine Surgery, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Med Sci Monit. 2020 May 21;26:e922928. doi: 10.12659/MSM.922928.
BACKGROUND The exosomes (Exo) derived from mesenchymal stem cells (MSCs) are capable of attenuating the apoptosis of nucleus pulposus cells (NPCs) elicited by proinflammatory cytokines. However, it remains unknown whether MSC-derived Exo also exert a protective effect on NPCs in the pathological acid environment. MATERIAL AND METHODS NPCs were divided into 3 groups: Group A, pH 7.1-7.3; Group B, pH 6.5-6.7 and Group C, pH 5.9-6.1. The NPCs were cultured in the above-defined acidic medium, and 3 different amounts of Exo were added into the media. Finally, the expression of the caspase-3, aggrecan, collagen II, and MMP-13 was analyzed and compared among the different groups. RESULTS Compared with cells cultured at pH 7.1-7.3 (Group A), proliferation activity of NPCs cultured at pH 5.9-6.7 (Group B and C) decreased significantly. Collagen II and aggrecan expression was also obviously reduced with the decrease of cell proliferation. Conversely, the expression of caspase-3 and MMP-13 significantly increased. Further experiments showed that proliferation activity was significantly attenuated in NPCs cultured at pH 5.9-6.1 without Exo treatment (Group E) compared with those cultured at pH 7.1-7.3 without Exo treatment (Group D). CONCLUSIONS In the pathological acid environment, MSC-derived Exo promotes the expression of chondrocyte extracellular matrix, collagen II, and aggrecan, and reduces matrix degradation by downregulating matrix-degrading enzymes, protecting NPCs from acidic pH-induced apoptosis. This study reveals a promising strategy for treatment of IVD degeneration.
间充质干细胞(MSCs)来源的外泌体(Exo)能够减轻促炎细胞因子诱导的髓核细胞(NPC)凋亡。然而,目前尚不清楚 MSC 来源的 Exo 是否对病理性酸性环境中的 NPC 也具有保护作用。
将 NPC 分为 3 组:A 组,pH7.1-7.3;B 组,pH6.5-6.7;C 组,pH5.9-6.1。将 NPC 在上述定义的酸性培养基中培养,并向培养基中加入 3 种不同量的 Exo。最后,分析和比较不同组之间 caspase-3、聚集蛋白聚糖、胶原 II 和基质金属蛋白酶 13 的表达。
与 pH7.1-7.3 培养的细胞(A 组)相比,pH5.9-6.7(B 组和 C 组)培养的 NPC 的增殖活性显著降低。随着细胞增殖的减少,胶原 II 和聚集蛋白聚糖的表达也明显减少。相反,caspase-3 和 MMP-13 的表达显著增加。进一步的实验表明,与 pH7.1-7.3 无外泌体处理(D 组)的 NPC 相比,在无外泌体处理的 pH5.9-6.1 中培养的 NPC 的增殖活性明显降低(E 组)。
在病理性酸性环境中,MSC 来源的 Exo 通过下调基质降解酶来促进软骨细胞细胞外基质、胶原 II 和聚集蛋白聚糖的表达,减少基质降解,从而保护 NPC 免受酸性 pH 诱导的凋亡。本研究为治疗椎间盘退变提供了一种有前途的策略。