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山东大学学报(医学版) ›› 2010, Vol. 48 ›› Issue (9): 59-63.

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血小板衍生生长因子对人脐带间充质干细胞胞外基质的影响

庄泳1, 李栋2, 时庆2, 汪大琨2, 蔡直锋1, 鞠秀丽1   

  1. 山东大学齐鲁医院 1.儿科;2.低温医学研究室, 济南 250012
  • 收稿日期:2010-03-29 出版日期:2010-09-16 发布日期:2010-09-16
  • 通讯作者: 鞠秀丽(1964- ),女,教授,博士生导师,主要从事儿科血液学专业研究。 E-mail: shellysdcn07@hotmail.com
  • 作者简介:庄泳(1984- ),男,硕士研究生,主要从事儿科血液学专业研究。
  • 基金资助:

    国家自然科学基金资助项目(30700163);山东省自然科学基金资助项目(Y2007C109);山东省科技攻关计划资助项目(2009GG10002027)。

Effects of the plateletderived growth factor on proliferation and extracellularmatrix of human umbilical cord mesenchymal stem cells

ZHUANG Yong1,  LI Dong2,  SHI Qing2,  WANG Da-kun2,  CAI Zhi-feng1,  JU Xiu-li1   

  1. 1. Department of Pediatrics; 2. Cryomedicine Lab, Qilu Hospital of Shandong University, Jinan 250012, China
  • Received:2010-03-29 Online:2010-09-16 Published:2010-09-16

摘要:

目的     探讨血小板衍生生长因子(PDGF)对人脐带间充质干细胞(UCMSCs)增殖和细胞外基质(ECM)表达的影响及其可能的作用机制。方法     体外传代培养UCMSCs,分为对照组和实验组,其中对照组不加PDGF,实验组分别加入不同质量浓度(2、5、10、20、50μg/L)的PDGF。加入PDGF 12h后,用qRT-PCR法检测ECM基因和凋亡相关基因(Bcl2、Bax)的表达;加入PDGF 24h后,用四甲基偶氮唑(MTT)法检测细胞增殖。结果    与对照组比较,随着PDGF质量浓度的增加,反映细胞代谢活性的OD值逐渐增加,且PDGF质量浓度在20μg/L时达到最高值,但PDGF质量浓度为50μg/L时OD值反而降低;PDGF质量浓度为2μg/L时,ECM表达和Bcl2/Bax比值较对照组有所降低,随着PDGF质量浓度的增加,ECM的表达和Bcl2/Bax比值呈现先增高后降低的趋势,且在10μg/L时达到最高值。 结论     PDGF可以促进脐带间充质干细胞的增殖,同时能促进其ECM的表达,还能提高细胞耐受凋亡的能力,最佳作用质量浓度为10μg/L。

关键词: 脐带;间充质干细胞;血小板衍生生长因子;细胞外基质

Abstract:

Objective    To investigate the effects of the platelet-derived growth factor(PDGF) on the proliferation, extracellular matrix  synthesis and its probable mechanism in human umbilical cord mesenchymal stem cells(UCMSCs). Methods    Cultured UCMSCs were divided into 6 groups: the control group, and the PDGF-treated groups(2, 5, 10, 20 and 50μg/L).  Morphological changes of the cells were observed under an inverted microscope.  MTT assay was used to detect the PDGF effects on cell proliferation.  Expressions of ECM mRNA and apoptosis-related genes(Bcl-2, Bax)were detected by qRT-PCR. Results    With an increased concentration of PDGF, UCMSCs proliferation was gradually promoted compared with the control group. 20μg/L PDGF greatly promoted UCMSCs proliferation, however, 50μg/L showed  inhibitive effects. Expressions of ECM mRNA and apoptosis-related factor (Bcl-2/Bax) were down-regulated in the 2μg/L PDGF group but up-regulated when PDGF≥5μg/L. 10μg/L PDGF greatly upregulated ECM mRNA expression and apoptosis-related factor (Bcl2/Bax). Conclusion    PDGF can promote the proliferation of UCMSCs, stimulate ECM synthesis and improve the ability to withstand apoptosis of UCMSCs in vitro. 10μg/L PDGF was the most effective concentration.

Key words: Cord; Mesenchymal stem cells; Plateletderived growth factor; Extracellular matrix

中图分类号: 

  • Q291
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