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|本期目录/Table of Contents|

小鼠内皮祖细胞的分离、培养与定向诱导分化(PDF)

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2009年第4期
页码:
503-506
栏目:
基础研究
出版日期:
2009-06-25

文章信息/Info

Title:
Isolation, culture and identification of mesenchymal stem cells and endothelial progenitor cells from murine bone marrow
作者:
王云雅1; 顾春虎2; 汪静1; 邓敬兰11; 袁梦晖1; 李国权1; 赵壁君2
第四军医大学西京医院： 1.核医学科,2.心脏外科，陕西 西安 710032
Author(s):
WANG Yun-ya1;  GU Chun-hu2;  WANG Jing1;  DENG Jing-lan1;  YUAN Meng-hui1;  LI Guo-quan1;  ZHAO Bi-jun2
1.Department of Nuclear Medicine, 2.Department of Cardiovascular Surgery, Xijing Hospital, Fourth Military Medical University, Xian 710032, Shaanxi, China
关键词:
骨髓; 内皮祖细胞; 细胞培养
Keywords:
bone marrow;  endothelial progenitor cell;  cell culture
分类号:
Q254
DOI:
-
文献标识码:
A
摘要:
目的 建立一种稳定、高效，从小鼠骨髓中分离培养与定向诱导分化内皮祖细胞(EPCs)的方法。方法 从小鼠骨髓中密度梯度离心法分离单个核细胞,经差速贴壁结合特殊培养基扩增并向内皮细胞定向诱导分化EPCs。应用免疫荧光和流式细胞技术鉴定内皮细胞系列标志:CD34、CD31、Flk-1和祖细胞标志CD133。并通过检测其对FITC标记的UEA-1的吸附和内吞DiI-ac-LDL来进行细胞功能学的鉴定。对分化细胞行vWF、CD31 免疫组化染色鉴定，并与血管内皮细胞合成前列腺素能力进行比较。结果 经过梯度密度离心和贴壁法选择的细胞表达内皮细胞特异性抗原CD34、CD31、Flk-1,部分表达CD133。分离所得细胞经EBM-2专用培养基培养后，第4天可见集落形成，培养第9天流式细胞仪检测其CD34、CD133、CD31、Flk-1阳性率分别为(44±4)%、(18±3)%、(49±4)%和(79±6)%，细胞能特异性吸附FITC标记的荆豆凝集素并内吞DiI-ac-LDL,约3周左右可融合近80%，形成铺路石样内皮细胞特有形态。传代后vWF、CD31免疫组化染色阳性率分别为(66±5)%和(56±5)%。诱导后的内皮祖细胞的合成前列腺素能力与血管内皮细胞之间无显著差异。结论 从小鼠骨髓中分离培养与定向诱导分化EPCs的方法，效率高，稳定性和重复性好。
Abstract:
AIM: To establish an efficient and stable method for simultaneous isolation, culture and differentiation of murine endothelial progenitor cells (EPCs) from bone marrow. METHODS: Mononuclear cells were isolated from murine bone marrow by density gradient (Histopaque-1077, Sigma) after differential centrifugation. The resulting cells were cultured and differentiated to endothelial cells (ECs) in EBM-2. The expressions of specific antigens (CD133, CD34, Flk-1 and CD31) on cell surface were analyzed by immunofluorescence and flow cytometer. Biological functions of endothelial cells were examined by the adsorption of ulex europaeus-agglutinin (UEA) labeled by fluorescein isothiocyanate (FITC) and DiI-ac-LDL internalization. Expression of vWF and CD31 of ECs differentiated from EPCs was also assessed by immunohistochemistry. RESULTS: Cells were obtained from mouse bone marrow by density gradient, and adhesive cells expressed CD133, CD34 and Flk-1 and formed clusters at the 4th day. At the 14th day, UEA adsorption was labeled by FITC and DiI-ac-LDL internalization were positive. Expression of CD133 in adhesive cells decreased, whereas CD31 increased. Positive ratios of CD34+, CD133+, Flk-1+ and CD31+ were (43.55±4.12)%, (18.29±2.56)%, (48.78±3.96)% and (78.89±6.38)%, respectively. After 3 weeks, they differentiated into mature ECs forming cobblestone monolayers. There was no difference in secretion of PGI2 between ECs from EPCs and ECs from mouse aorta. CONCLUSION: An efficient, stable and replicable method for simultaneous isolation and culture of MSCs and EPCs from a single mouse has been established.

参考文献/References

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备注/Memo

备注/Memo:
收稿日期：2008-2-21.基金项目：国家自然科学基金项目资助（30600137）；陕西省攻关课题资助［2007K13-03（3）］ 通讯作者：顾春虎，主治医生，博士，主要从事组织工程、心血管保护等研究Email：guchuhu@fmmu.edu.cn 作者简介：王云雅，主管技师Email：yunyaw@126.com
更新日期/Last Update: 2009-06-15