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本文引用的文献

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Fibroblast growth factor 2 positively regulates expression of activating transcription factor 4 in osteoblasts.成纤维细胞生长因子 2 正向调节成骨细胞中激活转录因子 4 的表达。
Biochem Biophys Res Commun. 2010 Jan 1;391(1):335-9. doi: 10.1016/j.bbrc.2009.11.059. Epub 2009 Nov 12.
2
BMP2 signaling in bone development and repair.BMP2 信号在骨骼发育和修复中的作用。
Cytokine Growth Factor Rev. 2009 Oct-Dec;20(5-6):475-80. doi: 10.1016/j.cytogfr.2009.10.018. Epub 2009 Nov 4.
3
Mineralized tissue formation by BMP2-transfected pulp stem cells.经骨形态发生蛋白2转染的牙髓干细胞形成矿化组织
J Dent Res. 2009 Nov;88(11):1020-5. doi: 10.1177/0022034509346258.
4
Immortalization and characterization of mouse floxed Bmp2/4 osteoblasts.小鼠floxed Bmp2/4成骨细胞的永生化及特性分析
Biochem Biophys Res Commun. 2009 Aug 14;386(1):89-95. doi: 10.1016/j.bbrc.2009.05.144. Epub 2009 Jun 6.
5
Influences of reduced expression of maternal bone morphogenetic protein 2 on mouse embryonic development.母体骨形态发生蛋白2表达降低对小鼠胚胎发育的影响。
Sex Dev. 2008;2(3):134-41. doi: 10.1159/000143431. Epub 2008 Sep 3.
6
BMP2 regulates Osterix through Msx2 and Runx2 during osteoblast differentiation.在成骨细胞分化过程中,骨形态发生蛋白2(BMP2)通过Msx2和Runx2调节osterix。
J Biol Chem. 2008 Oct 24;283(43):29119-25. doi: 10.1074/jbc.M801774200. Epub 2008 Aug 14.
7
Molecular consequences of a frameshifted DLX3 mutant leading to Tricho-Dento-Osseous syndrome.导致毛发-牙-骨综合征的移码型DLX3突变体的分子后果。
J Biol Chem. 2008 Jul 18;283(29):20198-208. doi: 10.1074/jbc.M709562200. Epub 2008 May 19.
8
Characterization of human dental pulp-derived cell lines.人牙髓来源细胞系的特性分析。
Int Endod J. 2008 Jul;41(7):609-16. doi: 10.1111/j.1365-2591.2008.01409.x. Epub 2008 May 12.
9
Bone morphogenetic protein 2 mediates dentin sialophosphoprotein expression and odontoblast differentiation via NF-Y signaling.骨形态发生蛋白2通过NF-Y信号传导介导牙本质涎磷蛋白表达和成牙本质细胞分化。
J Biol Chem. 2008 Jul 11;283(28):19359-70. doi: 10.1074/jbc.M709492200. Epub 2008 Apr 18.
10
Structural coupling of Smad and Runx2 for execution of the BMP2 osteogenic signal.Smad与Runx2的结构偶联以执行BMP2成骨信号
J Biol Chem. 2008 Mar 28;283(13):8412-22. doi: 10.1074/jbc.M705578200. Epub 2008 Jan 18.

永生化小鼠 Bmp2 牙乳头间充质细胞系保持成牙本质细胞表型并对 BMP2 作出反应。

Immortalized mouse floxed Bmp2 dental papilla mesenchymal cell lines preserve odontoblastic phenotype and respond to BMP2.

机构信息

Department of Pediatric Dentistry, Dental School, The University of Texas Health Science Center, San Antonio, Texas 78229-3900, USA.

出版信息

J Cell Physiol. 2010 Oct;225(1):132-9. doi: 10.1002/jcp.22204.

DOI:10.1002/jcp.22204
PMID:20458728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2980836/
Abstract

Bone morphogenetic protein 2 (Bmp2) is essential for odontogensis and dentin mineralization. Generation of floxed Bmp2 dental mesenchymal cell lines is a valuable application for studying the effects of Bmp2 on dental mesenchymal cell differentiation and its signaling pathways during dentinogenesis. Limitation of the primary culture of dental mesenchymal cells has led to the development of cell lines that serve as good surrogate models for the study of dental mesenchymal cell differentiation into odontoblasts and mineralization. In this study, we established and characterized immortalized mouse floxed Bmp2 dental papilla mesenchymal cell lines, which were isolated from 1st mouse mandibular molars at postnatal day 1 and immortalized with pSV40 and clonally selected. These transfected cell lines were characterized by RT-PCR, immunohistochemistry, and analyzed for alkaline phosphatase activity and mineralization nodule formation. One of these immortalized cell lines, iBmp2-dp, displayed a higher proliferation rate, but retained the genotypic and phenotypic characteristics similar to primary cells as determined by expression of tooth-specific markers as well as demonstrated the ability to differentiate and form mineralized nodules. In addition, iBmp2-dp cells were inducible and responded to BMP2 stimulation. Thus, we for the first time described the establishment of an immortalized mouse floxed Bmp2 dental papilla mesenchyma cell line that might be used for studying the mechanisms of dental cell differentiation and dentin mineralization mediated by Bmp2 and other growth factor signaling pathways.

摘要

骨形态发生蛋白 2(Bmp2)对于牙发生和牙本质矿化是必不可少的。生成 floxed Bmp2 牙间质细胞系是研究 Bmp2 对牙间质细胞分化及其在牙本质发生过程中的信号通路影响的有价值的应用。牙间质细胞原代培养的局限性导致了细胞系的发展,这些细胞系可以作为研究牙间质细胞分化为成牙本质细胞和矿化的良好替代模型。在本研究中,我们建立并鉴定了永生化的 floxed Bmp2 牙乳头间质细胞系,这些细胞系是从出生后第 1 天的第 1 下颌磨牙中分离出来的,并用 pSV40 永生化并进行克隆选择。这些转染细胞系通过 RT-PCR、免疫组织化学进行了鉴定,并分析了碱性磷酸酶活性和矿化结节形成。这些永生化细胞系中的一个,iBmp2-dp,表现出更高的增殖率,但保留了与原代细胞相似的基因型和表型特征,如牙特异性标志物的表达,以及显示出分化和形成矿化结节的能力。此外,iBmp2-dp 细胞可诱导并对 BMP2 刺激产生反应。因此,我们首次描述了建立一种永生化的 mouse floxed Bmp2 牙乳头间质细胞系,该细胞系可用于研究 Bmp2 和其他生长因子信号通路介导的牙细胞分化和牙本质矿化的机制。