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Mechano-transduction in osteoblastic cells involves strain-regulated estrogen receptor alpha-mediated control of insulin-like growth factor (IGF) I receptor sensitivity to Ambient IGF, leading to phosphatidylinositol 3-kinase/AKT-dependent Wnt/LRP5 receptor-independent activation of beta-catenin signaling.成骨细胞中的机械转导涉及应变调节的雌激素受体 α 介导的对环境 IGF 中 IGF-I 受体敏感性的控制,导致磷脂酰肌醇 3-激酶/AKT 依赖性 Wnt/LRP5 受体非依赖性激活β-连环蛋白信号通路。
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Early activation of the beta-catenin pathway in osteocytes is mediated by nitric oxide, phosphatidyl inositol-3 kinase/Akt, and focal adhesion kinase.成骨细胞中β-连环蛋白途径的早期激活是由一氧化氮、磷脂酰肌醇-3 激酶/Akt 和粘着斑激酶介导的。
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Prostaglandin promotion of osteocyte gap junction function through transcriptional regulation of connexin 43 by glycogen synthase kinase 3/beta-catenin signaling.前列腺素通过糖原合酶激酶 3/β-连环蛋白信号转导对连接蛋白 43 的转录调控促进骨细胞缝隙连接功能。
Mol Cell Biol. 2010 Jan;30(1):206-19. doi: 10.1128/MCB.01844-08.
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Regulatory roles of beta-catenin and AP-1 on osteoprotegerin production in interleukin-1alpha-stimulated periodontal ligament cells.β-连环蛋白和活化蛋白-1在白细胞介素-1α刺激的牙周膜细胞中对骨保护素产生的调节作用
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Role of Wnt signaling in the biology of the periodontium.Wnt 信号通路在牙周组织生物学中的作用。
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Putative signaling action of amelogenin utilizes the Wnt/beta-catenin pathway.釉原蛋白的假定信号传导作用利用Wnt/β-连环蛋白途径。
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Beta-catenin levels influence rapid mechanical responses in osteoblasts.β-连环蛋白水平影响成骨细胞的快速力学反应。
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机械加载激活牙周膜细胞中的 β-连环蛋白信号通路。

Mechanical loading activates β-catenin signaling in periodontal ligament cells.

机构信息

Orthodontic Section, Department of Growth and Development, University of Nebraska Medical Center College of Dentistry, Lincoln, NE 68583, USA.

出版信息

Angle Orthod. 2011 Jul;81(4):592-9. doi: 10.2319/090310-519.1. Epub 2011 Feb 7.

DOI:10.2319/090310-519.1
PMID:21299429
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8919760/
Abstract

OBJECTIVE

To determine whether β-catenin signaling is responsive to mechanical loading in periodontal ligament (PDL) cells.

MATERIALS AND METHODS

To determine whether Wnt/β-catenin signaling pathway components are present and functional, PDL cells were treated with lithium chloride or Wnt3a-conditioned media. To determine whether mechanical strain activates β-catenin signaling, PDL cells were subjected to compressive loading. Activation of the β-catenin signaling pathway was determined by immunofluorescence, Western immunoblotting, and TOPflash assay.

RESULTS

Mimicking Wnt signaling stimulates β-catenin nuclear translocation and T-cell factor/lymphoid enhancer binding factor-dependent transcriptional activation in PDL cells. Mechanical loading stimulates a transient accumulation of dephosphorylated β-catenin in the cytoplasm and its translocation to the nucleus. This effect of strain acts through activation of protein kinase B and phosphorylation of glycogen synthase kinase-3 beta. These strain-related changes do not involve the low-density lipoprotein receptor-related protein 5/Wnt receptor.

CONCLUSIONS

The Wnt/β-catenin signaling pathway components are functional and activated by mechanical loading in PDL cells. β-catenin serves as an effector of mechanical signals in PDL cells.

摘要

目的

确定β-连环蛋白信号是否对牙周韧带(PDL)细胞中的机械加载有反应。

材料和方法

为了确定 Wnt/β-连环蛋白信号通路的组成部分是否存在且具有功能,用氯化锂或 Wnt3a 条件培养基处理 PDL 细胞。为了确定机械应变是否激活β-连环蛋白信号,将 PDL 细胞进行压缩加载。通过免疫荧光、Western 免疫印迹和 TOPflash 测定来确定β-连环蛋白信号通路的激活情况。

结果

模拟 Wnt 信号刺激 PDL 细胞中β-连环蛋白的核转位和 T 细胞因子/淋巴增强因子结合因子依赖性转录激活。机械加载刺激细胞质中去磷酸化的β-连环蛋白的瞬时积累,并使其向核内转位。这种应变的作用通过蛋白激酶 B 的激活和糖原合成激酶-3β的磷酸化来实现。这些与应变相关的变化不涉及低密度脂蛋白受体相关蛋白 5/Wnt 受体。

结论

Wnt/β-连环蛋白信号通路的组成部分在 PDL 细胞中是有功能的,并可被机械加载激活。β-连环蛋白是 PDL 细胞中机械信号的效应物。