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作 者:章少华[1] 劳杰[1] 李岩峰[1] 顾玉东[1] 赵新[1] 李继峰[1]
机构地区:[1]复旦大学附属华山医院手外科,上海200040
出 处:《中华手外科杂志》2009年第2期110-112,共3页Chinese Journal of Hand Surgery
基 金:国家973计划课题基金资助项目(2005CB522604);上海市周围神经显微外科重点实验室课题基金资助项目(05DE22108)
摘 要:目的寻找简单快速获得高纯度雪旺细胞的方法。方法取20只预变性成年SD大鼠坐骨神经,经分次酶消化后,分别使用DMEM/F12(A组)和黑素细胞培养基(B组)进行培养。冷喷射(cold jet)方式传代,S-100染色鉴定。结果采用黑素细胞培养基组的雪旺细胞纯度达到90%以上。结论使用黑素细胞培养基及冷喷射传代操作简单,可以在短期内获得足量高纯度的雪旺细胞。Objective To develop a simple and effective method to obtain highly purified Schwann cells. Methods After enzymatic digestion of Predegenerated sciatic nerves from 20 adult SD rats were with 1 week ion, the suspension were cultured in group A (DMEM/F12 medium) and group B (melanocyte growth medium), cold jet as the passage method. S-100 stain for detection of Schwann cell purity. Results The cell yields and purity of group B was beyond 90%. Conclusion The combination of melanocyte growth medium and cold jet provides a convenient mean to obtain considerable Schwann cells with purity.
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