Xing Wen, Pang Ai-Ming, Yao Jian-Feng, Li Yuan, Shi Hui, Sheng Meng-Yao, Zhou Yuan, Zhao Ying-Xu, Xu Ming-Jiang, Yang Feng-Chun
Chinese Academy of Medical Sciences, Tianjin, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013 Apr;21(2):451-4. doi: 10.7534/j.issn.1009-2137.2013.02.040.
Human bone marrow is the major source of mesenchymal stem cells (MSC). It was reported that the standard density gradient centrifugation method was not efficient in isolating MSC and it may be caused by the existing of bone marrow particles. In previous study, a lot of MSC were obtained by culturing bone marrow particles alone combined with standard method. However, it is time- and labor-consuming to obtain bone marrow particles by filtering and to isolate MNC by density gradient centrifugation. This study was purposed to explore the more simple and efficient method to isolate MSC from bone marrow. Seven normal bone marrow aspirates were collected and centrifugated. The bone marrow particles floated on surface layers were cultured by modified primary explant culture, whereas the bone marrow aspirates deposited were cultured by direct plating method, then the immun phenotype and differentiation capability of isolated cells were analyzed. The results showed that in 3 of 7 aspirates, bone marrow particles were floated on surface layers, whereas the other bone marrow cells and some particles were deposited after centrifugation. The MSC were reliably isolated from the floating layers or deposited aspirates by modified primary explant culture and direct plating method separately. After 3 passages the isolated MSC did not express CD45 and CD34, but expressed CD105, CD73, CD44, CD90, CD49e and they could differentiate into chondrocytes and adipocytes. It is concluded that normal human bone marrow MSC can be isolated simply and efficiently by direct plating method in combination with modified primary explant culture.
人骨髓是间充质干细胞(MSC)的主要来源。据报道,标准密度梯度离心法分离MSC的效率不高,这可能是由于骨髓颗粒的存在所致。在先前的研究中,通过单独培养骨髓颗粒并结合标准方法获得了大量MSC。然而,通过过滤获得骨髓颗粒并通过密度梯度离心分离单核细胞既耗时又费力。本研究旨在探索从骨髓中分离MSC的更简单有效的方法。收集7份正常骨髓抽吸物并进行离心。对漂浮在表层的骨髓颗粒采用改良的原代外植体培养法进行培养,而对沉淀的骨髓抽吸物采用直接接种法进行培养,然后分析分离细胞的免疫表型和分化能力。结果显示,在7份抽吸物中有3份,骨髓颗粒漂浮在表层,而其他骨髓细胞和一些颗粒在离心后沉淀。通过改良的原代外植体培养法和直接接种法分别从漂浮层或沉淀的抽吸物中可靠地分离出MSC。传代3次后,分离出的MSC不表达CD45和CD34,但表达CD105、CD73、CD44、CD90、CD49e,并且它们可以分化为软骨细胞和脂肪细胞。结论是,结合改良的原代外植体培养法,采用直接接种法可简单高效地分离正常人骨髓MSC。