• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Bmp4 通过调控细胞增殖和凋亡对牙尖形态的改变。

Cuspal Shape Alterations by Bmp4 Directing Cell Proliferation and Apoptosis.

机构信息

Division in Anatomy and Developmental Biology, Department of Oral Biology, Taste Research Center, Oral Science Research Center, BK21 FOUR Project, Yonsei University College of Dentistry, Seoul, Korea.

NGeneS Inc., Ansan-si, Korea.

出版信息

J Dent Res. 2023 Jul;102(7):825-834. doi: 10.1177/00220345231167769. Epub 2023 May 29.

DOI:10.1177/00220345231167769
PMID:37246809
Abstract

The enamel knot (EK), located at the center of cap stage tooth germs, is a transitory cluster of nondividing epithelial cells. The EK acts as a signaling center that provides positional information for tooth morphogenesis and regulates the growth of tooth cusps. To identify species-specific cuspal patterns, this study analyzed the cellular mechanisms in the EK that were related to bone morphogenetic protein (Bmp), which plays a crucial role in cell proliferation and apoptosis. To understand the cellular mechanisms in the EK, the differences between 2 species showing different cuspal patterning, mouse (pointy bunodont cusp) and gerbil (flat lophodont cusp), were analyzed with quantitative reverse transcriptase polymerase chain reaction and immunofluorescent staining. Based on these, we performed protein-soaked bead implantation on tooth germs of the 2 different EK regions and compared the cellular behavior in the EKs of the 2 species. Many genes related with cell cycle, cell apoptosis, and cell proliferation were involved in BMP signaling in the EK during tooth development. A comparison of the cell proliferation and apoptosis associated with Bmp revealed distinctive patterns of the cellular mechanisms. Our findings indicate that the cellular mechanisms, such as cell proliferation and apoptosis, in the EK are related to Bmp4 and play an important role in tooth morphogenesis.

摘要

釉结(EK)位于帽状期牙胚的中心,是一群暂不分裂的上皮细胞。EK 充当信号中心,为牙齿形态发生提供位置信息,并调节牙尖的生长。为了确定具有物种特异性的牙尖模式,本研究分析了与骨形态发生蛋白(Bmp)相关的 EK 中的细胞机制,Bmp 在细胞增殖和细胞凋亡中发挥着关键作用。为了了解 EK 中的细胞机制,我们分析了表现出不同牙尖模式的两种物种(小鼠(尖形布龙都尖)和沙鼠(平形骆马尖))之间 EK 的差异,使用定量逆转录聚合酶链反应和免疫荧光染色。在此基础上,我们对两种不同 EK 区域的牙胚进行了蛋白浸泡珠植入,并比较了两种物种 EK 中的细胞行为。许多与细胞周期、细胞凋亡和细胞增殖相关的基因都参与了牙发育过程中 EK 中的 BMP 信号转导。对与 Bmp 相关的细胞增殖和凋亡的比较揭示了细胞机制的独特模式。我们的研究结果表明,EK 中的细胞机制,如细胞增殖和凋亡,与 Bmp4 有关,在牙齿形态发生中发挥着重要作用。

相似文献

1
Cuspal Shape Alterations by Bmp4 Directing Cell Proliferation and Apoptosis.Bmp4 通过调控细胞增殖和凋亡对牙尖形态的改变。
J Dent Res. 2023 Jul;102(7):825-834. doi: 10.1177/00220345231167769. Epub 2023 May 29.
2
The primary enamel knot determines the position of the first buccal cusp in developing mice molars.原发性釉结决定了发育中小鼠磨牙中第一个颊尖的位置。
Differentiation. 2007 Jun;75(5):441-51. doi: 10.1111/j.1432-0436.2006.00153.x. Epub 2007 Feb 16.
3
Inhibition of apoptosis in the primary enamel knot does not affect specific tooth crown morphogenesis in the mouse.抑制小鼠原发性釉结中的细胞凋亡不会影响特定的牙冠形态发生。
Int J Dev Biol. 2000 Jun;44(4):389-96.
4
Hippo pathway/Yap regulates primary enamel knot and dental cusp patterning in tooth morphogenesis.河马通路/Yes相关蛋白(Yap)在牙齿形态发生过程中调节原发性釉结和牙尖模式。
Cell Tissue Res. 2015 Nov;362(2):447-51. doi: 10.1007/s00441-015-2267-8. Epub 2015 Aug 29.
5
Cell cycle of the enamel knot during tooth morphogenesis.牙齿形态发生过程中釉结的细胞周期。
Histochem Cell Biol. 2018 Jun;149(6):655-659. doi: 10.1007/s00418-018-1666-9. Epub 2018 Apr 12.
6
Temporospatial tissue interactions regulating the regeneration of the enamel knot in the developing mouse tooth.调节发育中小鼠牙齿釉结再生的时空组织相互作用。
Differentiation. 2007 Feb;75(2):158-65. doi: 10.1111/j.1432-0436.2006.00122.x.
7
The role of APCDD1 in epithelial rearrangement in tooth morphogenesis.APCDD1在牙齿形态发生中上皮重排的作用。
Histochem Cell Biol. 2015 Oct;144(4):377-87. doi: 10.1007/s00418-015-1345-z. Epub 2015 Jul 14.
8
The transcription factor NKX2-3 mediates p21 expression and ectodysplasin-A signaling in the enamel knot for cusp formation in tooth development.转录因子 NKX2-3 介导 p21 表达和外胚层发育不良素-A 信号在牙发育中的牙尖形成牙釉质结中。
J Biol Chem. 2018 Sep 21;293(38):14572-14584. doi: 10.1074/jbc.RA118.003373. Epub 2018 Aug 8.
9
Identification of a novel putative signaling center, the tertiary enamel knot in the postnatal mouse molar tooth.在出生后小鼠磨牙中鉴定出一个新的假定信号中心——三级釉结。
Mech Dev. 2003 Mar;120(3):270-6. doi: 10.1016/s0925-4773(02)00458-6.
10
Modulation of activin/bone morphogenetic protein signaling by follistatin is required for the morphogenesis of mouse molar teeth.卵泡抑素对激活素/骨形态发生蛋白信号的调节是小鼠磨牙形态发生所必需的。
Dev Dyn. 2004 Sep;231(1):98-108. doi: 10.1002/dvdy.20118.

引用本文的文献

1
Identifying cell types by lasso-constraint regularized Gaussian graphical model based on weighted distance penalty.基于加权距离惩罚的lasso 约束正则化高斯图形模型识别细胞类型。
Brief Bioinform. 2024 Sep 23;25(6). doi: 10.1093/bib/bbae572.
2
PRX1-positive mesenchymal stem cells drive molar morphogenesis.PRX1 阳性间充质干细胞驱动磨牙形态发生。
Int J Oral Sci. 2024 Feb 19;16(1):15. doi: 10.1038/s41368-024-00277-0.