中国神经再生研究(英文版) ›› 2014, Vol. 9 ›› Issue (18): 1696-1702.doi: 10.4103/1673-5374.141805

• 原著:周围神经损伤修复保护与再生 • 上一篇    下一篇

皮肤来源前体细胞源性许旺细胞可促进大鼠损伤周围神经的再生

  

  • 收稿日期:2014-07-21 出版日期:2014-09-26 发布日期:2014-09-26
  • 作者简介:中国国家自然科学基金项目(81171194)

Schwann cells originating from skin-derived precursors promote peripheral nerve regeneration in rats

Ping Zhang 1, Xiaocheng Lu 2, Jianghai Chen 2, Zhenbing Chen 2   

  1. 1 Department of Orthopedics, Wuhan Women and Children Health Care Center, Wuhan, Hubei Province, China
    2 Department of Hand Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China
  • Received:2014-07-21 Online:2014-09-26 Published:2014-09-26
  • Contact: Zhenbing Chen, M.D., Ph.D., Department of Hand Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China, 2990430205@qq.com. Jianghai Chen, M.D., Ph.D., Department of Hand Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China, Chenjianghai2002@hotmail.com.
  • Supported by:

    This work was supported by the National Natural Science Foundation of China, No.  81171194.

摘要:

含有许旺细胞的人工导管能显著促进长距离周围神经缺损的再生,但原代许旺细胞不宜自体移植,皮肤源性前体细胞可在特定的条件下被诱导分化为许旺细胞。因此,实验提取成年大鼠背侧真皮中皮肤源性前体细胞,以含B27、神经调节蛋白1和forskolin的DMEM/F12诱导分化,免疫荧光染色及反转录PCR证实所获细胞为许旺细胞。进一步实验通过对比复合皮肤来源前体细胞、许旺细胞或皮肤来源前体细胞来源许旺细胞硅胶管桥接5mm坐骨神经缺损,发现皮肤来源前体细胞源性许旺细胞可明显促进坐骨神经轴突的再生,肌电图证实皮肤来源前体细胞源性许旺细胞移植后,大鼠损伤坐骨神经功能明显恢复,且效果优于复合皮肤来源前体细胞,但效果仍不及许旺细胞。说明皮肤来源前体细胞源性许旺细胞能促进大鼠损伤周围神经的再生。

关键词: 神经再生, 皮肤来源前体细胞, 许旺细胞, 周围神经损伤, 坐骨神经损伤, 细胞移植

Abstract:

Artificial guidance channels containing Schwann cells can promote the regeneration of injured peripheral nerve over long distances. However, primary Schwann cells are not suitable for autotransplantation. Under specific conditions, skin-derived progenitors can be induced to differentiate into Schwann cells. Therefore, adult rat dorsal skin (dermis)-derived progenitors were isolated and induced to differentiate with DMEM/F12 containing B27, neuregulin 1, and forskolin. Immunofluorescence staining and reverse transcription polymerase chain reaction (RT-PCR) confirmed that the resultant cells were indeed Schwann cells. Artificial guidance channels containing skin-derived progenitors, Schwann cells originating from skin-derived progenitors, or primary Schwann cells were used to bridge 5 mm sciatic nerve defects. Schwann cells originating from skin-derived progenitors significantly promoted sciatic nerve axonal regeneration. The significant recovery of injured rat sciatic nerve function after the transplantation of Schwann cells originating from skin-derived progenitors was confirmed by electromyogram. The therapeutic effect of Schwann cells originating from skin-derived progenitors was better than that of skin-derived progenitors. These findings indicate that Schwann cells originating from skin-derived precursors can promote peripheral nerve regeneration in rats.

Key words: erve regeneration, skin-derived precursors, Schwann cells, peripheral nerve injury, cell transplantation, NSFC grant, neural regeneration