Department of Spine Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200240, China.
Department of Orthopaedics, 987 Hospital of PLA, Xi'an, 721000, Shaanxi Province, China.
J Neuroinflammation. 2020 Mar 16;17(1):85. doi: 10.1186/s12974-020-01765-w.
A growing body of studies have indicated that bone marrow mesenchymal stem cells (BMSCs) have powerful analgesic effects in animal models of bone cancer pain. Here, we explored the molecular mechanisms underlying how BMSCs alleviate pain sensation in a mouse model of bone cancer pain.
C3H/HeN adult male mice were used to generate a bone cancer pain model. BMSCs were isolated from mouse bone marrow, modified by transfection with microRNA-9-5p (miR-9-5p), and infused into the spinal cord. Spontaneous flinches, paw withdrawal latency, limb-use score, and weight-bearing score were used to assess pain-related behaviors. ELISA, RT-PCR, western blot, and luciferase assay were used to assess gene expressions.
Our results show that miR-9-5p regulated the expression of both repressor element silencing transcription factor (REST) and μ-opioid receptors (MOR) by targeting REST in primary mouse BMSCs. Overexpression of miR-9-5p reversed the activation of inflammatory pathway in TNF-α- and IL-6-treated BMSCs. In addition, miR-9-5p modified BMSCs alleviated cancer pain in the sarcoma-inoculated mouse model. MiR-9-5p modified BMSCs suppressed cytokine expression in the spinal cord of sarcoma-inoculated mice by suppressing REST gene expression.
Our results indicate that miR-9-5p modified BMSCs can relieve bone cancer pain via modulating neuroinflammation in the central nervous system, suggesting genetically modified BMSCs could be a promising cell therapy in pain management.
越来越多的研究表明骨髓间充质干细胞(BMSCs)在骨癌痛动物模型中具有强大的镇痛作用。在这里,我们探讨了 BMSCs 缓解骨癌痛小鼠模型中疼痛感觉的分子机制。
使用 C3H/HeN 成年雄性小鼠生成骨癌痛模型。从鼠骨髓中分离 BMSCs,通过转染 microRNA-9-5p(miR-9-5p)进行修饰,并注入脊髓。自发性抽搐、足底退缩潜伏期、肢体使用评分和负重评分用于评估与疼痛相关的行为。ELISA、RT-PCR、western blot 和荧光素酶测定用于评估基因表达。
我们的结果表明,miR-9-5p 通过靶向 REST 在原代小鼠 BMSCs 中调节沉默转录因子(REST)和 μ 阿片受体(MOR)的表达。miR-9-5p 的过表达逆转了 TNF-α 和 IL-6 处理的 BMSCs 中炎症通路的激活。此外,miR-9-5p 修饰的 BMSCs 通过抑制 REST 基因表达减轻肉瘤接种小鼠的癌痛。miR-9-5p 修饰的 BMSCs 通过抑制脊髓中细胞因子的表达来减轻肉瘤接种小鼠的神经炎症。
我们的结果表明,miR-9-5p 修饰的 BMSCs 可以通过调节中枢神经系统中的神经炎症来缓解骨癌痛,这表明基因修饰的 BMSCs 可能是疼痛管理中一种有前途的细胞治疗方法。