期刊文献+

转化生长因子β促进面突外胚间充质干细胞向平滑肌细胞分化 被引量:1

The Positive Effect of Transforming Growth Factor β on Ectomesenchymal Stem Cells of Embryonic Facial Processes Differentiating to Smooth Muscle Cells
在线阅读 下载PDF
导出
摘要 目的 探讨转化生长因子 β(TGF_β)对面突外胚间充质干细胞向平滑肌细胞分化的影响。 方法 6 0pmol LTGF_β作用于面突外胚间充质干细胞 ,分别于 1d、2d后进行抗α平滑肌肌动蛋白 (α_SMA)单克隆抗体免疫组化图象分析检测 ,2d后定量RT_PCR检测α_SMAmRNA的表达。结果 免疫组化显示 ,TGF_β诱导组表达α_SMA的细胞数约为 95 % ,而未加分化抑制剂的自然分化组表达α_SMA的细胞数约为 6 5 %。图象分析显示 ,1d、2dTGF_β诱导组抗α_SMA着色平均灰度值小于未加分化抑制剂的自然分化组。定量RT_PCR显示TGF_β诱导组α_SMAmRNA量大于自然分化组。有分化抑制剂的对照组细胞不表达α_SMA。结论 TGF_β诱导组细胞表达α_SMA强于自然分化组。TGF_β可以促进外胚间充质干细胞向平滑肌细胞分化。 Objective To investigate the effect of transforming growth factor β(TGF-β)on ectomesenchymal stem cells differentiating to smooth muscle cells. Methods 60 pmol/L TGF-β was added to the ectomesenchymal stem cells of embryonic facial processes. Immunohistochemistry assay and image analysis were used to value the expression extent of α smooth muscle actin (α-SMA) and quantitative RT-PCR was used to value the quantity of α-SMA.Results 2 days later, about 95% cells in TGF-β group and 65% cells in control group without differentiation inhibitor expressed α-SMA. Expression of α-SMA in TGF-β group was stronger than that of control group after one and two days. Quantitative RT-PCR showed the quantity of α-SMA mRNA in treated group cells was more than that of in control group. Conclusion Quantity of α-SMA in TGF-β group is more than that of spontaneous differentiation group. TGF-β has positive effect on ectomesenchymal stem cells differentiating to smooth muscle cells.
出处 《华西口腔医学杂志》 CAS CSCD 北大核心 2004年第6期460-462,共3页 West China Journal of Stomatology
基金 第四军医大学创新工程重点课题资助项目 (CX 0 2F0 0 2 )
关键词 外胚间充质干细胞 转化生长因子 平滑肌细胞 分化 ectomesenchymal stem cell transforming growth factor β smooth muscle cell differentiation
  • 相关文献

参考文献11

  • 1Barlow AJ, Bogardi JP, Ladher R, et al. Expression of chick Barx-1 and its differential regulation by FGF-8 and BMP-4 signaling in the maxillary primordial[J]. Dev Dyn, 1999,214(4):291-302.
  • 2Shigetani Y, Nobusada Y, Kuratani S. Ectodermally derived FGF8 defines the maxillomandibular region in the early chick embryo: epithelial-mesenchymal interactions in the specification of the craniofacial ectomesenchyme[J]. Dev Biol, 2000,228(1):73-85.
  • 3Hautmann MB, Adam PJ, Owens GK. Similarities and differences in smooth muscle α-actin induction by TGF-β in smooth muscle versus non-srnonth muscle cells[J]. Arterioscler Thromb Vasc Bio1,1999,19(9): 2049-2058.
  • 4Shah NM, Groves AK, Anderson DJ. Alternative neural crest cell fates are instructively promoted by TGF-β superfamily members [J].Cell, 1996,85(3) :331-343.
  • 5Grainger DJ, Metcalfe JC, Grace AA, etal. Transforming growth factor-β dynamically regulates vascular smooth muscle differentiation in vivo[J]. J Cell Sci, 1998,111(19):2977-2988.
  • 6Clowes AW, Clowes MM, Kocher O, et al. Arterial smooth-muscle cellsin vivo-relationship between actin isoform expression and mitogenesis and their modulation by heparin[J]. J Cell Biol, 1988,107(5):1939-1945.
  • 7Owens GK, Geisteffer AA, Yang YW, et al. Transforming growth factor-beta-induced growth-inhibition and cellular hypertrophy in cultured vascular smooth-muscle cells[J]. J Cell Biol, 1988, 107(2):771-780.
  • 8Ronnov-Jessen L, Petersen OW. Induction of α-snooth muscle actin by transforming growth factor-β1 in quiescent humane breast gland fibroblast[J]. Lab Invest, 1993,68(6) :696-707.
  • 9Peehl DM, Sellers RG. Induction of smooth muscle cell phenotype in cultured humane prostatic stromal cells[J]. Exp Cell Res, 1997,232(2) :208-215.
  • 10Hirschi KK, Rohovsky SA, D'Amore PA. PDGF, TGF-β and heterotopic cell-cell interactions mediate endothelial cell-induced recruitment of 10T1/2 cells and their differentiation to a smooth muscle fate[J]. JCell Biol, 1998,141(3) :805-814.

同被引文献19

  • 1周泽渊,于淑湘,史俊南,张建平,金岩,尤苏霞.诱导颌突外胚间充质干细胞向成骨细胞分化[J].牙体牙髓牙周病学杂志,2007,17(3):125-128. 被引量:1
  • 2谷莉,秦瑞峰,郭滨,裴艳蕾,刘丽文,聂鑫.外胚间充质干细胞构建组织工程骨骼肌的应用研究[J].现代生物医学进展,2007,7(10):1464-1466. 被引量:2
  • 3Albini TA,Wang RC,Reiser B,et al.Microglial stability andrepopulation in the retina [J].Br J Ophthalmol,2005,89(7):901-903.
  • 4Rezaie P,Dean A,Male D,et al.Microglia in the cerebralwall of the human telencephalon at second trimester [J].Cereb Cortex,2005,15(7):938-949.
  • 5Tsuchiya T,Park KC,Toyonaga S,et al.Characterization ofmicroglia induced from mouse embryonic stem cells andtheir migration into the brain parenchyma [J].J Neuroim-munol,2005,160(1-2):210-218.
  • 6Grobben B,De Deyn PP,Siegers H.Rat C6 glioma as expe-rimental model system for the study of glioblastoma growthand invasion [J].Cell Tissue Res,2002,310(3):257-270.
  • 7Ziu M,Schmidt NO,Cargioli TG,et al.Glioma-producedextracellular matrix influences brain tumor tropism of hu-man neural stem cells [J].J Neurooncol,2006,79(2):125-133.
  • 8Kendall SE,Najbauer J,Johnston HF,et al.Neural stem ceiltargeting of glioma is dependent on phosphoinositide 3-kinase signaling [J].Stem Cells,2008; 26(6):1575-1586.
  • 9van der Meulen AA,Biber K,Lukovac S,et al.The role ofCXC chemokine ligand(CXCL)12-CXC chemokine receptor(CXCR)4 signalling in the migration of neural stem cellstowards a brain tumour [J].Neuropathol Appl Neurobiol,2009,35(6):579-591.
  • 10Xu Q,Yuan X,Xu M,et al.Chemokine CXC receptor 4-mediated glioma tumor tracking by bone marrow--derivedneural progenitor/stem cells [J].Mol Cancer Ther,2009,8(9):2746—2753.

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部