Platelet-derived growth factor promotes the proliferation of human umbilical cord-derived mesenchymal stem cells

被引:13
|
作者
Qiu, Pubin [1 ]
Song, Wencong [1 ]
Niu, Zhiwei [1 ]
Bai, Yaofu [1 ,2 ]
Li, Wei [2 ]
Pan, Shaohui [2 ]
Peng, Sha [1 ]
Hua, Jinlian [1 ]
机构
[1] Northwest A&F Univ, Coll Vet Med, Shaanxi Stem Cell Engn & Technol Res Ctr, Key Lab Anim Biotechnol Agr,Minist China, Yangling 712100, Peoples R China
[2] North Branch Biotechnol Co Ltd Jiangsu Prov, Taizhou 225300, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
umbilical cord mesenchymal stem cells (UC-MSCs); platelet-derived growth factor (PDGF); proliferation; human; EXPRESSION; EXPANSION; GENE; PDGF; MIGRATION; BLOOD;
D O I
10.1002/cbf.2870
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study was designed to investigate the effect of platelet-derived growth factor (PDGF) on the proliferation of human umbilical cord mesenchymal stem cells (UC-MSCs) and further explore the mechanism of PDGF in promoting the proliferation of UC-MSCs. The human UC-MSCs were treated with different concentrations of PDGF, and the effects were evaluated by counting the cell number, the cell viability, the expression of PDGF receptors analyzed by RT-PCR, and the detection of the gene expression of cell proliferation, cell cycle and pluripotency, and Brdu assay by immunofluorescent staining and Quantitative real-time (QRT-PCR). The results showed that PDGF could promote the proliferation of UC-MSCs in vitro in a dose-dependent way, and 10 to 50 ng/ml PDGF had a significant proliferation effect on UC-MSCs; the most obvious concentration was 50 ng/ml. Significant inhibition on the proliferation of UC-MSCs was observed when the concentration of PDGF was higher than 100 ng/ml, and all cells died when the concentration reached 200 ng/ml PDGF. The PDGF-treated cells had stronger proliferation and antiapoptotic capacity than the control group by Brdu staining. The expression of the proliferation-related genes C-MYC, PCNA and TERT and cell cyclerelated genes cyclin A, cyclin 1 and CDK2 were up-regulated in PDGF medium compared with control. However, pluripotent gene OCT4 was not significantly different between cells cultured in PDGF and cells analyzed by immunofluorescence and QRT-PCR. The PDGF could promote the proliferation of human UC-MSCs in vitro. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:159 / 165
页数:7
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