期刊文献+

BMP4对牙源性干细胞精氨酸组蛋白甲基化酶表达影响的研究 被引量:1

Effect of BMP4 on the expression of arginine histone methylase in dental tissue derived mesenchymal stem cells
下载PDF
导出
摘要 目的探索人重组骨形成蛋白4(BMP4)对牙源性干细胞精氨酸组蛋白甲基化酶表达的影响。方法利用BMP4对根尖牙乳头干细胞和牙周膜干细胞进行诱导,Real-time PCR检测精氨酸组蛋白甲基化酶基因家族的主要相关基因PMRT1~9的表达变化。结果 Real-time PCR结果显示50 ng/ml BMP4促进根尖牙乳头干细胞精氨酸组蛋白甲基化酶基因家族中的PRMT2、PRMT4、PRMT5、PRMT6、PRMT7和PRMT9的表达,而在牙周膜干细胞50 ng/ml BMP4只促进PRMT6的表达。结论 BMP4促进根尖牙乳头干细胞和牙周膜干细胞部分精氨酸组蛋白甲基化酶的表达,可能在牙源性干细胞成骨分化中起一定的作用。 Objective To examine the effect of human recombinant bone morphogenetic protein 4 (BMP4) on the expression of arginine histone methylase in dental tissue derived mesenehymal stem ceils. Methods BMP4 was used to induce the stem cells from apical papilla ( SCAPs ) and periodontal ligament stem cells ( PDLSCs ). The related gene expression of arginine histone methylase, including PRMT1-9, was examined by real-time PCR. Results After the induction of 50 ng/ml BMP4, the expression of PRMT2, PRMT4, PRMT5, PRMT6, PRMT7, and PRMT9 were up-regulated in SCAPs, while only PRMT6 expression was increased in PDLSCs after 50 ng/ml BMP4 treatment. Conclusion BMP4 promoted the expression of some arginine histone methylase in SCAPs and PDLSCs, which may play a role in the osteogenie differentiation of dental tissue derived MSCs.
出处 《北京口腔医学》 CAS 2017年第6期305-308,共4页 Beijing Journal of Stomatology
关键词 BMP4 根尖牙乳头干细胞 牙周膜干细胞 精氨酸 组蛋白甲基化酶 BMP4 SCAPs PDLSCs Arginine Histone methylase
  • 相关文献

参考文献4

二级参考文献58

  • 1包柳郁,金岩,史俊南,牛忠英,汪平,赵守亮,郝建军,王捍国.人牙源性间充质细胞向成牙本质细胞的诱导分化[J].实用口腔医学杂志,2005,21(2):178-182. 被引量:9
  • 2赵征,黄征难,徐军明.ADAM28真核表达质粒的构建及转染人牙囊细胞后的表达分析[J].上海口腔医学,2007,16(4):404-409. 被引量:7
  • 3Seo BM, Miura M, Gronthos S, et al. Investigation of multipotent postnatal stem ceils from human periodontal ligament. Lancet, 2004, 364(9429) : 149-155.
  • 4Howell TH, Martuscelli G, Oringer J. Polypeptide growth factors for periodontal regeneration. Curr Opin Periodontol, 1996,3 : 149-156.
  • 5Fan Z,Yamaza T, Lee JS, et al. BCOR regulates mesenchymal stem cell function by epigenetic mechanisms. Nat Cell Biol,2009,11 (8) : 1002-1009.
  • 6Du J,Ma Y,Ma P,et al. Demethylation of epiregulin gene by histone demethylase ibxlll and bcl6 corepressor inhibits osteo/dentinogenic differentiation. Stem Cells, 2012 Oct 16. doi: 10. 1002/stem. 1255. [ Epub ahead of print].
  • 7Toyoda H, Komurasaki T, Uchida D, et al. Distribution of mRNA for human epiregulin,a differentially expressed member of the epidermal growth factor family. Biochem J, 1997,326 (Pt 1 ) : 69-75.
  • 8Shirasawa S, Sugiyama S, Baba I, et al. Dermatitis due to epiregulin deficiency and a critical role of epiregulin in immune-related responses of kerafinocyte and macrophage. Proc Natl Acad Sci U S A, 2004,101 (38) : 13921-13926.
  • 9Draper BK, Komurasaki T, Davidson MK, et al. Epiregulin is more potent than EGF or TGFalpha in promoting in vitro wound closure due to enhanced ERK/MAPK activation. J Cell Biochem,2003,89 (6): 1126-1137.
  • 10Taylor DS, Cheng X, Pawlowski JE, et al. Epiregulin is a potent vascular smooth muscle cell-derived mitogen induced by angiotensin Ⅱ,endothelin-1 ,and thrombirL Proc Natl Acad Sci U S A, 1999,96 (4) : 1633-1638.

共引文献23

同被引文献2

引证文献1

二级引证文献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