相关实验视频
Updated: Sep 9, 2025

10:26
Inducing Apical Periodontitis in Mice
Published on: August 6, 2019
12.3K
根吸收中的信号通路:连接炎症,口腔细胞生成和组织重塑
Golriz Rostami1, Rajeshwari Hadagalu Revana Siddappa1, Anil Kishen2
1The Kishen Lab, Dental Research Institute, University of Toronto, Toronto, Canada.
Journal of endodontics
|August 30, 2025
概括
牙根再吸收涉及牙根组织的口腔细胞分解,类似于骨再吸收. 信号通路和炎症调解器对这一过程具有关键作用, 影响正牙和创伤性牙损伤.
科学领域:
- 牙科生物学
- 细胞生物学
- 病理学
背景情况:
- 根吸收是一种病理过程,在这种过程中,口腔细胞会分解牙和水泥.
- 这一过程反映了骨质细胞驱动的骨再吸收,涉及复杂的分子信号.
- 了解这些机制对于治疗像正牙根再吸收这样的疾病至关重要.
研究的目的:
- 综合审查涉及根吸收的分子信号通路和媒介.
- 分析促炎和抗炎因素在牙周细胞分化和活性中的作用.
- 突出影响再吸收抵抗的根结构的独特方面.
主要方法:
- 对调节骨质细胞形成和口腔细胞形成的信号通路的文献综述.
- 分析促炎和抗炎细胞因子的作用.
- 检查细胞外矩阵重塑因子和机械传导.
主要成果:
- 骨质细胞生成由RANK/RANKL/OPG轴,Wnt和炎症体通路进行调节.
- 支持炎症的调解剂 (例如IL-1,TNF-α) 促进了口腔细胞的分化,而抗炎细胞因子 (例如IL-4,IL-10) 则抑制了分化.
- 矩阵金属蛋白酶和环蛋白调节细胞外矩阵,而炎症微环境是关键.
结论:
- 根吸收涉及复杂的吸收和修复因子之间的交叉声.
- 炎症微环境和特定的信号通路决定了根部退化的程度.
- 独特的根结构提供一些抵抗力, 但炎症和机械刺激驱动吸收.
相关概念视频
Role Of Notch Signalling In Intestinal Stem Cell Renewal
2.2K
Notch signaling was first discovered in Drosophila melanogaster, where it is involved in cell lineage differentiation. Notch signaling regulates the maintenance and differentiation of intestinal stem cells or ISCs by controlling the expression of atonal homolog 1 or Atoh1. Atoh1 directs cells to differentiate into secretory cells.
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
2.2K
Notch Signaling Pathway
4.4K
The Notch signaling pathway is a major intracellular signaling pathway that is highly conserved over a broad spectrum of metazoan species. It stands unique from other intracellular signaling mechanisms in animals because notch protein itself acts as the receptor as well as the primary signaling molecule.
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
4.4K
Osteoclasts in Bone Remodeling
3.2K
Osteoclasts are cells responsible for bone resorption and remodeling. They originate from hematopoietic progenitor cells present in the bone marrow. Numerous progenitor cells fuse to form multinucleated cells, each with 10-20 nuclei. A single osteoclast has a diameter of 150 to 200 µM. These cells have ruffled borders that break down the underlying bone tissue and release minerals such as calcium into the blood in bone resorption. Osteoclasts cling to bones with their ruffled edges during...
3.2K
TGF - β Signaling Pathway
7.6K
The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors...
7.6K
Bone Remodeling
38.5K
Bone remodeling is a continuous and balanced process of bone resorption by osteoclasts and bone formation by osteoblasts. In adults, it helps maintain bone mass and calcium homeostasis. While mechanical stress can stimulate turnover as part of the normal maintenance and reparative process, several hormones also regulate bone remodeling.
38.5K
The JAK-STAT Signaling Pathway
9.2K
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as SH2...
9.2K

