首页> 外文期刊>Neural regeneration research >Folic acid contributes to peripheral nerve injury repair by promoting Schwann cell proliferation, migration, and secretion of nerve growth factor
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Folic acid contributes to peripheral nerve injury repair by promoting Schwann cell proliferation, migration, and secretion of nerve growth factor

机译:叶酸通过促进雪旺氏细胞的增殖,迁移和神经生长因子的分泌来促进周围神经损伤的修复

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After peripheral nerve injury, intraperitoneal injection of folic acid improves axon quantity, increases axon density and improves electromyography results. However, the mechanisms for this remain unclear. This study explored whether folic acid promotes peripheral nerve injury repair by affecting Schwann cell function. Primary Schwann cells were obtained from rats by in vitro separation and culture. Cell proliferation, assayed using the Cell Counting Kit-8 assay, was higher in cells cultured for 72 hours with 100 mg/L folic acid compared with the control group. Cell proliferation was also higher in the 50, 100, 150, and 200 mg/L folic acid groups compared with the control group after culture for 96 hours. Proliferation was markedly higher in the 100 mg/L folic acid group compared with the 50 mg/L folic acid group and the 40 ng/L nerve growth factor group. In Transwell assays, the number of migrated Schwann cells dramatically increased after culture with 100 and 150 mg/L folic acid compared with the control group. In nerve growth factor enzyme-linked immunosorbent assays, treatment of Schwann cell cultures with 50, 100, and 150 mg/L folic acid increased levels of nerve growth factor in the culture medium compared with the control group at 3 days. The nerve growth factor concentration of Schwann cell cultures treated with 100 mg/L folic acid group was remarkably higher than that in the 50 and 150 mg/L folic acid groups at 3 days. Nerve growth factor concentration in the 10, 50, and 100 mg/L folic acid groups was higher than that in the control group at 7 days. The nerve growth factor concentration in the 50 mg/L folic acid group was remarkably higher than that in the 10 and 100 mg/L folic acid groups at 7 days. In vivo, 80 μg/kg folic acid was intraperitoneally administrated for 7 consecutive days after sciatic nerve injury. Immunohistochemical staining showed that the number of Schwann cells in the folic acid group was greater than that in the control group. We suggest that folic acid may play a role in improving the repair of peripheral nerve injury by promoting the proliferation and migration of Schwann cells and the secretion of nerve growth factors.
机译:周围神经损伤后,腹膜内注射叶酸可改善轴突数量,增加轴突密度并改善肌电图检查结果。但是,其机制尚不清楚。这项研究探讨了叶酸是否通过影响雪旺细胞功能来促进周围神经损伤的修复。通过体外分离和培养从大鼠获得原代雪旺氏细胞。与对照组相比,使用Cell Counting Kit-8分析法检测的细胞增殖在用100 mg / L叶酸培养72小时的细胞中更高。培养96小时后,在50、100、150和200 mg / L的叶酸组中,细胞增殖也高于对照组。叶酸100 mg / L组的增殖明显高于叶酸50 mg / L和神经生长因子40 ng / L组。在Transwell分析中,与对照组相比,分别用100和150 mg / L叶酸培养后,迁移的雪旺氏细胞数量急剧增加。在神经生长因子酶联免疫吸附试验中,与对照组相比,在第3天,用50、100和150 mg / L叶酸处理Schwann细胞培养物可增加培养基中神经生长因子的水平。叶酸组100 mg / L处理3天后神经细胞生长因子浓度明显高于50和150 mg / L叶酸组。叶酸10、50和100 mg / L组的神经生长因子浓度在第7天高于对照组。叶酸50 mg / L组的神经生长因子浓度在第7天明显高于叶酸10和100 mg / L组。在体内,坐骨神经损伤后连续7天腹膜内施用80μg/ kg的叶酸。免疫组织化学染色显示,叶酸组的雪旺氏细胞数量大于对照组。我们建议,叶酸可能通过促进雪旺细胞的增殖和迁移以及神经生长因子的分泌来改善周围神经损伤的修复。

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