连小峰,侯铁胜,傅强,袁健东,金根洋,陈元贵.植块法与酶消化法结合培养原代大鼠雪旺细胞[J].中国脊柱脊髓杂志,2008,(9):.
植块法与酶消化法结合培养原代大鼠雪旺细胞
Study of culturing primary Schwann cells of rats by explant and enzyme digestion technique Identification of melatonin receptor in human bone mesenchymals stromal cells and its significance
  
DOI:
中文关键词:  雪旺细胞  细胞培养  消化法  植块法
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基金项目:国家自然科学基金,上海市青年科技启明星计划
连小峰  侯铁胜  傅强  袁健东  金根洋  陈元贵
上海市长海医院骨科,200433
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中文摘要:
  目的:探讨利用植块法与酶消化法相结合培养大鼠原代雪旺细胞的可行性;并研究其增殖规律.方法:取10只新生2~3d的SD大鼠双侧坐骨神经;剥除神经外膜;剪成约1mm3大小的碎块;用0.03%胶原酶和0.25%胰蛋白酶按1:2对神经碎块消化12min;加入少量含10%胎牛血清的DMED培养基小心吹打细胞及组织块;再植于培养皿中培养.用S-100免疫组化染色鉴定雪旺细胞;结合Hoechst3342染色计算其纯度;在显微镜下确定细胞数量.结果:在植块培养24h后即有大量细胞迁出;2~6d细胞生长迅速;10d以后生长较为缓慢;其倍增时间为2-3d.经S-100染色证实所培养细胞为雪旺细胞;结合Hoechst3342染色可得其培养8d时纯度为95.1%;传代后纯度可达96.3%.10只新生鼠培养12d后可得细胞数约为4.8×106个.结论:利用植块法与酶消化法相结合的方法可以迅速获得大量高纯度的雪旺细胞;其增殖速度在前6d最快;倍增时间为2.3d.
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