首页> 外文期刊>Journal of reconstructive microsurgery >Autogenous venous graft with one-stage prepared schwann cells as a conduit for repair of long segmental nerve defects.
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Autogenous venous graft with one-stage prepared schwann cells as a conduit for repair of long segmental nerve defects.

机译:自体静脉移植物,经一步制备的施旺细胞作为修复长节段神经缺损的导管。

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The use of autogenous venous graft with intraluminal injection of Schwann cells to enhance nerve regeneration of long segmental nerve defects was evaluated in a rabbit tibial nerve-repair model. Schwann cells were isolated from the excised rabbit tibial nerve by using the polylysine differential adhesion method. The cultured cells were identified by immunocytochemical labeling for S-100 protein. Tibial nerve defects in 4-cm segments were created in 24 animals, which were then divided into three groups. In Group 1, the tibial nerve defect was repaired with interposition vein graft alone; in Group 2, the nerve defect was repaired with a vein graft with intraluminal injection of Schwann-cell suspension; in Group 3, the nerve defect was repaired by autogenous nerve graft alone. At 2 months postoperatively, electrophysiologic evaluation showed that an evoked muscle action potential was recorded for the animals in Group 2, with vein grafting plus Schwann cells, and for those in Group 3, with autogenous nerve grafting, but not for those in Group 1, where vein grafting alone was used. The average motor nerve conduction velocity in the group with vein grafting and Schwann cells was 3.4 +/- 1.5 m/sec, which was slower than the nerve grafting group (7.8 +/- 1.8 m/sec). Histologic analysis confirmed there was formation of new nerve fascicles with myelination in the vein graft filled with Schwann cells. No nerve regrowth was found in the vein grafts without Schwann cells. These results suggested that isolated Schwann cells are able to survive in a vein graft, and that the vein graft with intraluminal seeded Schwann cells could be an alternative for repairing injured nerves with long gaps.
机译:在兔胫神经修复模型中评估了自体静脉移植物腔内注射施万细胞对增强长节段神经缺损的神经再生的作用。使用聚赖氨酸差异粘附法从切除的兔胫神经中分离出雪旺细胞。通过免疫细胞化学标记S-100蛋白鉴定培养的细胞。在24只动物中产生了4厘米长的胫骨神经缺损,然后将其分为三组。在第1组中,仅通过介入静脉移植修复了胫骨神经缺损。在第2组中,腔内注射施万细胞悬浮液通过静脉移植修复神经缺损。在第三组中,仅通过自体神经移植修复了神经缺损。术后2个月,电生理评估显示,第2组动物经静脉移植加雪旺氏细胞记录了诱发的肌肉动作电位,第3组动物自体神经移植记录了诱发的肌肉动作电位,但第1组动物未记录到。仅使用静脉移植的地方静脉移植和雪旺氏细胞组的平均运动神经传导速度为3.4 +/- 1.5 m / sec,比神经移植组(7.8 +/- 1.8 m / sec)慢。组织学分析证实,在充满施万细胞的静脉移植物中形成了新的神经束,髓鞘化。没有雪旺氏细胞的静脉移植物中未发现神经再生长。这些结果表明,分离的雪旺氏细胞能够在静脉移植物中存活,并且腔内植入雪旺氏细胞的静脉移植物可以替代修复具有长间隙的神经。

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