• 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

骨桥蛋白在牙周组织矿化和非矿化组织中的定位与表达。

Localization and expression of osteopontin in mineralized and nonmineralized tissues of the periodontium.

作者信息

MacNeil R L, Berry J, D'Errico J, Strayhorn C, Somerman M J

机构信息

Department of Periodontics/Prevention and Geriatrics, School of Dentistry, University of Michigan, Ann Arbor 48109-1078, USA.

出版信息

Ann N Y Acad Sci. 1995 Apr 21;760:166-76. doi: 10.1111/j.1749-6632.1995.tb44628.x.

DOI:10.1111/j.1749-6632.1995.tb44628.x
PMID:7785893
Abstract

To summarize results from various studies focusing on determining the expression/localization of BSP and OPN during tooth root development, there is general agreement that OPN is expressed/localized to the root surface during cementogenesis and is also seen throughout the PDL region. The expression/localization of OPN to odontoblasts and its role in dentinogenesis is less apparent. Recent studies directed at establishing odontoblast cell lines should help to resolve this conflict. Studies on BSP expression during tooth root formation indicate a very precise expression and localization of this molecule during cementogenesis indicating that this molecule may play an important role in the formation of this mineralized tissue. However, as with OPN, the expression of BSP and its role in dentin formation is not clearly defined.

摘要

为总结各项聚焦于确定牙骨质生成过程中骨涎蛋白(BSP)和骨桥蛋白(OPN)表达及定位的研究结果,普遍认为在牙骨质形成过程中OPN表达于/定位于牙根表面,并且在整个牙周韧带区域也可见到。OPN在成牙本质细胞中的表达/定位及其在牙本质形成中的作用则不太明显。针对建立成牙本质细胞系的近期研究应有助于解决这一矛盾。关于牙根形成过程中BSP表达的研究表明,该分子在牙骨质形成过程中有非常精确的表达和定位,这表明该分子可能在这种矿化组织的形成中发挥重要作用。然而,与OPN一样,BSP的表达及其在牙本质形成中的作用尚未明确界定。

相似文献

1
Localization and expression of osteopontin in mineralized and nonmineralized tissues of the periodontium.骨桥蛋白在牙周组织矿化和非矿化组织中的定位与表达。
Ann N Y Acad Sci. 1995 Apr 21;760:166-76. doi: 10.1111/j.1749-6632.1995.tb44628.x.
2
Role of two mineral-associated adhesion molecules, osteopontin and bone sialoprotein, during cementogenesis.两种与矿物质相关的黏附分子骨桥蛋白和骨唾液蛋白在牙骨质形成过程中的作用。
Connect Tissue Res. 1995;33(1-3):1-7. doi: 10.3109/03008209509016974.
3
Developmental appearance and distribution of bone sialoprotein and osteopontin in human and rat cementum.骨唾液蛋白和骨桥蛋白在人和大鼠牙骨质中的发育表现及分布
Anat Rec. 1998 Jan;250(1):13-33. doi: 10.1002/(SICI)1097-0185(199801)250:1<13::AID-AR3>3.0.CO;2-F.
4
Mineralization defects in cementum and craniofacial bone from loss of bone sialoprotein.因骨涎蛋白缺失导致的牙骨质和颅面骨矿化缺陷。
Bone. 2015 Sep;78:150-64. doi: 10.1016/j.bone.2015.05.007. Epub 2015 May 9.
5
Employing a transgenic animal model to obtain cementoblasts in vitro.利用转基因动物模型在体外获得成牙骨质细胞。
J Periodontol. 2000 Jan;71(1):63-72. doi: 10.1902/jop.2000.71.1.63.
6
Overlapping functions of bone sialoprotein and pyrophosphate regulators in directing cementogenesis.骨涎蛋白和焦磷酸盐调节剂在指导成牙骨质过程中的重叠功能。
Bone. 2017 Dec;105:134-147. doi: 10.1016/j.bone.2017.08.027. Epub 2017 Sep 1.
7
Models for the study of cementogenesis.牙骨质生成研究模型。
Connect Tissue Res. 1995;33(1-3):9-17. doi: 10.3109/03008209509016975.
8
Cementum attachment protein enriches putative cementoblastic populations on root surfaces in vitro.
J Dent Res. 2000 Jul;79(7):1482-8. doi: 10.1177/00220345000790070901.
9
Bone sialoprotein in developing porcine dental tissues: cellular expression and comparison of tissue localization with osteopontin and osteonectin.发育中的猪牙组织中的骨唾液蛋白:细胞表达以及与骨桥蛋白和骨粘连蛋白的组织定位比较
Arch Oral Biol. 1993 Mar;38(3):241-9. doi: 10.1016/0003-9969(93)90034-j.
10
Immunolocalization of osteopontin, osteocalcin, and dentin sialoprotein during dental root formation and early cementogenesis in the rat.大鼠牙根形成和早期牙骨质生成过程中骨桥蛋白、骨钙素和牙本质涎蛋白的免疫定位
J Bone Miner Res. 1994 Jun;9(6):833-41. doi: 10.1002/jbmr.5650090609.

引用本文的文献

1
lncRNA RNA AC114812 Regulates the Inflammatory Response of Periodontal Ligament Cells via the miR-181a-5p-SPP1 Axis.长链非编码RNA AC114812通过miR-181a-5p-SPP1轴调控牙周膜细胞的炎症反应
J Inflamm Res. 2025 Sep 19;18:13039-13053. doi: 10.2147/JIR.S534691. eCollection 2025.
2
The Bone Sialoprotein RGD Domain Modulates and Maintains Periodontal Development.骨涎蛋白 RGD 结构域调节和维持牙周发育。
J Dent Res. 2022 Sep;101(10):1238-1247. doi: 10.1177/00220345221100794. Epub 2022 Jun 9.
3
Enzyme replacement therapy prevents dental defects in a model of hypophosphatasia.
酶替代疗法可预防低磷酸酯酶症模型中的牙齿缺陷。
J Dent Res. 2011 Apr;90(4):470-6. doi: 10.1177/0022034510393517. Epub 2011 Jan 6.
4
Phosphorylated proteins and control over apatite nucleation, crystal growth, and inhibition.磷酸化蛋白与对磷灰石成核、晶体生长及抑制的控制。
Chem Rev. 2008 Nov;108(11):4670-93. doi: 10.1021/cr0782729. Epub 2008 Oct 3.
5
In vitro models of periodontal cells: a comparative study of long-term gingival, periodontal ligament and alveolar bone cell cultures in the presence of beta-glycerophosphate and dexamethasone.牙周细胞的体外模型:在β-甘油磷酸酯和地塞米松存在下长期牙龈、牙周韧带和牙槽骨细胞培养的比较研究
J Mater Sci Mater Med. 2007 Jun;18(6):1079-88. doi: 10.1007/s10856-007-0134-1. Epub 2007 Feb 1.