Mimura Toshiro, Dezawa Mari, Kanno Hiroshi, Sawada Hajime, Yamamoto Isao
Department of Neurosurgery, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
J Neurosurg. 2004 Nov;101(5):806-12. doi: 10.3171/jns.2004.101.5.0806.
Bone marrow stromal cells (BMSCs) can be induced to form Schwann cells by sequentially treating the cells with beta-mercaptoethanol and retinoic acid, followed by forskolin and neurotrophic factors including heregulin. In this study the authors made artificial grafts filled with BMSC-derived Schwann cells (BMSC-DSCs) and transplanted them into the transected sciatic nerve in adult rats to evaluate the potential of BMSCs as a novel alternative method of peripheral nerve regeneration.
The BMSC-DSCs were suspended in Matrigel and transferred into hollow fibers (12 mm in length), which were transplanted into the transected sciatic nerve in adult Wistar rats. Six months after cell transplantation, electrophysiological evaluation and walking track analysis were performed. Results of these studies showed significant improvement in motor nerve conduction velocity and sciatic nerve functional index in the BMSC-DSC-transplanted group compared with the control group (Matrigel graft only). Immunohistochemical study data demonstrated that transplanted BMSCs labeled with retrovirus green fluorescent protein were positive for P0 and myelin-associated glycoprotein and had reconstructed nodes of Ranvier and remyelinated regenerated nerve axons. The number of regenerated axons in the axial section of the central portion of the graft was significantly greater in the transplanted group. Although BMSCs can differentiate into several types of cells, tumor formation did not occur 6 months after engraftment.
Results in this study indicate that BMSC-DSCs have great potential to promote regeneration of peripheral nerves. The artificial graft made with BMSC-DSCs represents an alternative method for the difficult reconstruction of a long distance gap in a peripheral nerve.
通过依次用β-巯基乙醇和视黄酸处理骨髓基质细胞(BMSCs),随后用福斯可林和包括这里gulin在内的神经营养因子处理,可诱导BMSCs形成雪旺细胞。在本研究中,作者制作了填充有BMSC衍生雪旺细胞(BMSC-DSCs)的人工移植物,并将其移植到成年大鼠横断的坐骨神经中,以评估BMSCs作为外周神经再生新替代方法的潜力。
将BMSC-DSCs悬浮在基质胶中,转移到中空纤维(长度为12毫米)中,然后将其移植到成年Wistar大鼠横断的坐骨神经中。细胞移植6个月后,进行电生理评估和行走轨迹分析。这些研究结果显示,与对照组(仅基质胶移植物)相比,BMSC-DSC移植组的运动神经传导速度和坐骨神经功能指数有显著改善。免疫组织化学研究数据表明,用逆转录病毒绿色荧光蛋白标记的移植BMSCs对P0和髓鞘相关糖蛋白呈阳性,并且重建了郎飞结并使再生神经轴突重新髓鞘化。移植组移植物中央部分轴向切片中再生轴突的数量明显更多。尽管BMSCs可以分化为几种类型的细胞,但移植后6个月未发生肿瘤形成。
本研究结果表明,BMSC-DSCs具有促进外周神经再生的巨大潜力。用BMSC-DSCs制作的人工移植物代表了一种在外周神经长距离间隙困难重建中的替代方法。