SMAD公司
细胞生物学
运行x2
成牙本质细胞
信号转导
牙本质涎磷蛋白
牙本质形成
骨形态发生蛋白2
骨形态发生蛋白
BMPR2型
生物
化学
牙本质
转录因子
遗传学
医学
牙科
基因
体外
作者
Mengmeng Liu,Graham Goldman,Mary MacDougall,Shuo Chen
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2022-07-16
卷期号:11 (14): 2216-2216
被引量:35
标识
DOI:10.3390/cells11142216
摘要
BMP signaling plays an important role in dentin development. BMPs and antagonists regulate odontoblast differentiation and downstream gene expression via canonical Smad and non-canonical Smad signaling pathways. The interaction of BMPs with their receptors leads to the formation of complexes and the transduction of signals to the canonical Smad signaling pathway (for example, BMP ligands, receptors, and Smads) and the non-canonical Smad signaling pathway (for example, MAPKs, p38, Erk, JNK, and PI3K/Akt) to regulate dental mesenchymal stem cell/progenitor proliferation and differentiation during dentin development and homeostasis. Both the canonical Smad and non-canonical Smad signaling pathways converge at transcription factors, such as Dlx3, Osx, Runx2, and others, to promote the differentiation of dental pulp mesenchymal cells into odontoblasts and downregulated gene expressions, such as those of DSPP and DMP1. Dysregulated BMP signaling causes a number of tooth disorders in humans. Mutation or knockout of BMP signaling-associated genes in mice results in dentin defects which enable a better understanding of the BMP signaling networks underlying odontoblast differentiation and dentin formation. This review summarizes the recent advances in our understanding of BMP signaling in odontoblast differentiation and dentin formation. It includes discussion of the expression of BMPs, their receptors, and the implicated downstream genes during dentinogenesis. In addition, the structures of BMPs, BMP receptors, antagonists, and dysregulation of BMP signaling pathways associated with dentin defects are described.
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