[1]徐 斌,刘 毅. 不同分离方法及培养条件对人脐带间充质干细胞生物活性的影响[J].中国美容医学,2020,(2):71-73.
 XU Bin,LIU Yi. Effects of Separation Methods and Culture Conditions on Biological Characteristicsof Human Umbilical Cord-mesenchymal Stem Cells[J].Medical Aesthetics and Beauty,2020,(2):71-73.
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 不同分离方法及培养条件对人脐带间充质干细胞生物活性的影响
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《中国美容医学》[ISSN:1008-6445/CN:61-1347/R]

卷:
期数:
2020年2期
页码:
71-73
栏目:
出版日期:
2020-03-15

文章信息/Info

Title:
 Effects of Separation Methods and Culture Conditions on Biological Characteristics
of Human Umbilical Cord-mesenchymal Stem Cells
文章编号:
1008-6455(2020)02-0071-03
作者:
 徐 斌1刘 毅2
Author(s):
 XU Bin1LIU Yi2
关键词:
 [关键词]组织块贴壁法酶消化法人脐带间充质干细胞培养基生物活性
Keywords:
 Key words: tissue adherence method collagenase digestion method human umbilical cord-mesenchymal stemcells(hUCMSCs) culture medium biological characteristics
分类号:
Q813.1
文献标志码:
A
摘要:
[摘要]目的:观察不同分离方法及培养条件对人脐带间充质干细胞(Human umbilical cord-mesenchymal stem cells,
hUCMSCs)生物活性的影响。方法:分别用组织块贴壁法、酶消化法获取hUCMSCs,进行原代培养,记录各组首次传代时间,
相差显微镜观察细胞的形态,流式细胞仪鉴定其CD29、CD44、HLA-ABC、CD34、CD45、HLA-DR抗原表达。分别用DMEM-LG、
DMEM-HG和DMEM-F12 3种培养基培养第3代、第7代细胞,MTT法比较不同时间点3种培养基培养细胞的生长情况。结果:两
种分离方法均能得到较均一的梭形或者多角形贴壁细胞,胞核大胞浆丰富,CD29、CD44、HLA-ABC抗原表达阳性,CD34、
CD45、HLA-DR抗原表达阴性。用DMEM-F12培养的细胞活力更好,细胞生长更迅速。结论:两种分离方法均能得到hUCMSCs,
DMEM-F12培养基更能够促进细胞的增殖,较适合于培养hUCMSCs。

Abstract:
Abstract: Objective To observe the effects of different separation methods and culture conditions on biological characteristics
of hUCMSCs. Methods The hUCMSCs were isolated form human umbilical cord by tissue adherence and digested with
collagenase, the time of passage was recorded, in addition, the cell morphology was observed by phase contrast microscope,
and the CD29、CD44、HLA-ABC、CD34、CD45、HLA-DR antigen expression was identifi ed using fl ow cytometry. The
3rd and the 7th generation cells were cultured with DMEM-LG, MEM-HG, and DMEM-F12 culture medium. MTT was used to
evaluate the growth of hUCMSCs. Phase contrast microscope was used to observe the morphological changes of aging cells.
Results hUCMSCs could be separated by each method. The adherent cells showed shuttle or multiple angle shapes, with rich
cytoplasm, and positive for CD29、CD44、 HLA-ABC antigen, negative for CD34、CD45 and HLA-DR. DMEM-F12 could
promote the proliferation of quiescent cells. And the cells presented the better viability. Conclusion Both of the two methods
can produce hUCMSCs, DMEM-F12 medium is more suitable for the culture of hUCMSCs.

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更新日期/Last Update: 2020-03-31