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The role of the SIBLING, Bone Sialoprotein in skeletal biology - Contribution of mouse experimental genetics.SIBLING家族成员骨唾液蛋白在骨骼生物学中的作用——小鼠实验遗传学的贡献
Matrix Biol. 2016 May-Jul;52-54:60-77. doi: 10.1016/j.matbio.2015.12.011. Epub 2016 Jan 5.
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Enhanced Dentinogenesis of Pulp Progenitors by Early Exposure to FGF2.早期暴露于FGF2增强牙髓祖细胞的牙本质形成
J Dent Res. 2015 Nov;94(11):1582-90. doi: 10.1177/0022034515599768. Epub 2015 Aug 14.
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Runx2: Structure, function, and phosphorylation in osteoblast differentiation.Runx2:成骨细胞分化中的结构、功能和磷酸化。
Int J Biol Macromol. 2015;78:202-8. doi: 10.1016/j.ijbiomac.2015.04.008. Epub 2015 Apr 13.
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Stage-specific effects of fibroblast growth factor 2 on the differentiation of dental pulp cells.成纤维细胞生长因子2对牙髓细胞分化的阶段特异性作用。
Cells Tissues Organs. 2014;199(5-6):311-28. doi: 10.1159/000371343. Epub 2015 Mar 25.
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The Fibroblast Growth Factor signaling pathway.成纤维细胞生长因子信号通路。
Wiley Interdiscip Rev Dev Biol. 2015 May-Jun;4(3):215-66. doi: 10.1002/wdev.176. Epub 2015 Mar 13.
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Role and regulation of RUNX2 in osteogenesis.RUNX2在骨生成中的作用与调控。
Eur Cell Mater. 2014 Oct 23;28:269-86. doi: 10.22203/ecm.v028a19.
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Runx2 activity in committed osteoblasts is not essential for embryonic skeletogenesis.在已定向分化的成骨细胞中,Runx2活性对于胚胎骨骼发生并非必不可少。
Connect Tissue Res. 2014 Aug;55 Suppl 1(0 1):102-6. doi: 10.3109/03008207.2014.923873.
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Treatment of FGF-2 on stem cells from inflamed dental pulp tissue from human deciduous teeth.成纤维细胞生长因子-2对人乳牙牙髓炎症组织来源干细胞的作用
Oral Dis. 2014 Mar;20(2):191-204. doi: 10.1111/odi.12089. Epub 2013 Mar 18.
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Effects of growth factors on dental stem/progenitor cells.生长因子对牙源性干/祖细胞的影响。
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10
The role of runt-related transcription factor 2 (Runx2) in the late stage of odontoblast differentiation and dentin formation. runt 相关转录因子 2(Runx2)在成牙本质细胞分化和牙本质形成的晚期阶段的作用。
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成纤维细胞生长因子信号传导可防止成牙本质细胞的终末分化。

FGF Signaling Prevents the Terminal Differentiation of Odontoblasts.

作者信息

Sagomonyants K, Kalajzic I, Maye P, Mina M

机构信息

1 Department of Oral Health and Diagnostic Sciences, School of Dental Medicine, University of Connecticut Health Center, Farmington, CT, USA.

2 Department of Reconstructive Sciences, School of Dental Medicine, University of Connecticut Health Center, Farmington, CT, USA.

出版信息

J Dent Res. 2017 Jun;96(6):663-670. doi: 10.1177/0022034517691732. Epub 2017 Feb 7.

DOI:10.1177/0022034517691732
PMID:28170285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5444616/
Abstract

Members of the fibroblast growth factor (FGF) family play essential and important roles in primary and reparative dentinogenesis, with conflicting results regarding their effects on odontoblast differentiation. Our recent studies showed that the effects of FGF2 on cells in odontoblast lineage were stage-specific and depended on the stage of cell maturity. Continuous exposure of pulp cells to FGF2 inhibited odontoblast differentiation, whereas early and limited exposure of pulp cells to FGF2 resulted in marked increases in odontoblast differentiation. The purpose of this study was to evaluate the cellular and molecular mechanisms regulating the inhibitory effects of FGF2 on odontoblast differentiation. To do so, we examined the effects of the addition of FGF2 during the differentiation/mineralization phase of the in vitro growth of pulp cultures derived from a series of green fluorescent protein reporter transgenic mice that display stage-specific activation of transgenes during odontoblast differentiation. Our results showed that this treatment first stimulated the differentiation of remaining progenitors in pulp cultures into functional odontoblasts but prevented their differentiation into mature odontoblasts. In addition, this treatment inhibited expression of markers of osteogenesis. Furthermore, we demonstrated that the inhibitory effects of FGF2 on odontoblast differentiation were mediated through activation of FGFR/MEK/Erk1/2 signaling and downregulation of bone morphogenetic protein signaling, with negative and positive roles in the expression of Dmp1 and Dspp, respectively, during the advanced stage of odontoblast differentiation.

摘要

成纤维细胞生长因子(FGF)家族成员在原发性和修复性牙本质形成过程中发挥着至关重要的作用,但其对成牙本质细胞分化的影响却存在相互矛盾的结果。我们最近的研究表明,FGF2对成牙本质细胞谱系中的细胞的影响具有阶段特异性,并且取决于细胞成熟的阶段。牙髓细胞持续暴露于FGF2会抑制成牙本质细胞分化,而牙髓细胞早期和有限地暴露于FGF2会导致成牙本质细胞分化显著增加。本研究的目的是评估调节FGF2对成牙本质细胞分化抑制作用的细胞和分子机制。为此,我们在源自一系列绿色荧光蛋白报告转基因小鼠的牙髓培养物的体外生长的分化/矿化阶段添加FGF2,这些转基因小鼠在成牙本质细胞分化过程中显示出转基因的阶段特异性激活。我们的结果表明,这种处理首先刺激了牙髓培养物中剩余祖细胞分化为功能性成牙本质细胞,但阻止了它们分化为成熟的成牙本质细胞。此外,这种处理抑制了成骨标志物的表达。此外,我们证明FGF2对成牙本质细胞分化的抑制作用是通过激活FGFR/MEK/Erk1/2信号传导和下调骨形态发生蛋白信号传导介导的,在成牙本质细胞分化的晚期阶段,分别对Dmp1和Dspp的表达起负向和正向作用。