猪骨髓间质干细胞的分离培养及分化潜能的鉴定  

Isolation and culture of multipotent mesenchymal stem cells from porcine bone marrow

作　　者：方利君[1] 付小兵[2] 孙同柱[2] 李建福[2] 程飚[2] 王玉新[3] 

机构地区：[1]中国医科大学第二医院口腔科,辽宁沈阳110003 [2]解放军第三○四医院全军创伤修复重点实验室,北京100037 [3]中国医科大学第一医院口腔颌面外科,辽宁沈阳110001

出　　处：《中国危重病急救医学》2003年第10期606-608,共3页Chinese Critical Care Medicine

基　　金：国家重大基础研究规划资助项目 ( 19990 5 42 0 4);国家自然科学基金 ( 3 0 170 966);国家自然科学基金 ( 3 0 2 3 0 3 70 )

摘　　要：目的 :建立猪骨髓间质干细胞 (MSCs)的体外分离培养和鉴定的方法 ,探讨体外培养的间充质干细胞的一些生物学特点 ,为利用猪的实验研究提供实验基础。方法 :猪的髂嵴穿刺吸取骨髓 ,经密度梯度离心得到骨髓单个核细胞 ,接种后形成单层贴壁的成纤维样的细胞。检测细胞周期 ,多向诱导分化鉴定分离的细胞。结果 :体外培养的原代 MSCs 12～ 14 d达到融合 ,传代后仍具有分化成骨的能力 ,细胞周期显示有 80 %的细胞处于G0 / G1期。结论 :体外培养猪的 MSCs具有分化成骨的潜能 ,生长稳定 ,传代后仍保持未分化状态 .猪骨髓间充质干细胞分离培养体系的建立为基础研究和组织工程提供了一个有价值的动物模型。Objective:To establish a method for the isolation of porcine mesenchymal stem cells(MSCs) from bone marrow and to demonstrate their differentiation ex vivo into various mesenchymal tissue cells. Methods:MSCs were isolated from bone marrow and purified by centrifuge and in vitro.The proliferation and growth characteristics were observed in primary and passage culture.Cell cycle was analyzed by measuring DNA content with FACScan flow cytometer and cell multipotent was identified with specific staining. Results:The adherent,fibroblast-like cells were confluent in single layer after plating for 12~14 days.The cultured MSCs in vitro differentiated into osteoblasts.The cell cycle analysis showed that 80% of MSCs were in G0/G1 phase.Conclusion:Porcine MSCs can be isolated from postnatal bone marrow through their adherent ability.Porcine MSCs may be introduced as a valuable model system to study the mesenchymal lineages for basic research and tissue engineering.

关 键 词：骨髓间充质干细胞 细胞培养 猪 

分 类 号：R329[医药卫生—人体解剖和组织胚胎学]