• 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

人牙龈结合上皮体外再生过程中细胞表型的变化。

Changes in cell phenotype during regeneration of junctional epithelium of human gingiva in vitro.

作者信息

Salonen J I, Kautsky M B, Dale B A

出版信息

J Periodontal Res. 1989 Nov;24(6):370-7. doi: 10.1111/j.1600-0765.1989.tb00885.x.

DOI:10.1111/j.1600-0765.1989.tb00885.x
PMID:2480439
Abstract

The relationship between cell attachment and the phenotype of the attached oral epithelial cells was studied by comparing junctional epithelium (JE) with a culture model for JE in which epithelial cells form an equivalent organization of tissues. Gingival explants were cultured on either a high or a low protein-binding membrane. The cut edge of epithelium and connective tissue was placed on the membrane; epithelial cells migrated to form a sheet of tissue between the explant and the membrane substratum. Cells which grew in contact with the high protein-binding membrane attached to the substratum and assumed a cuboidal shape. With time in culture these cells showed a decrease in reactivity with antibodies to psi-3 antigen (an antigen associated with epithelial migration) and an increase in reactivity with antibodies to cytokeratin 19 (a marker for JE). Cells grown on the low protein-binding membrane did not exhibit changes in shape or antigens. Because similar features were found in the JE in vivo, it was concluded that the junctional cells which are directly attached to the tooth (DAT cells) have a nonmigratory phenotype that develops as a response to the tooth surface. Because the cells are in contact with a metabolically inert material the changes appear to be largely self-induced. The culture method allows studies on putative inducer molecules and on mechanisms which may control the phenotype of epithelial cells at the dentogingival interface.

摘要

通过将结合上皮(JE)与JE的培养模型进行比较,研究了细胞附着与附着的口腔上皮细胞表型之间的关系,在该培养模型中上皮细胞形成了等效的组织结构。牙龈外植体在高蛋白结合膜或低蛋白结合膜上培养。上皮和结缔组织的切缘置于膜上;上皮细胞迁移,在植体和膜基质之间形成一层组织。与高蛋白结合膜接触生长的细胞附着于基质并呈立方形。随着培养时间的延长,这些细胞与psi-3抗原(一种与上皮迁移相关的抗原)抗体的反应性降低,与细胞角蛋白19(JE的标志物)抗体的反应性增加。在低蛋白结合膜上生长的细胞在形状或抗原方面未表现出变化。由于在体内JE中发现了类似特征,得出的结论是,直接附着于牙齿的结合细胞(DAT细胞)具有非迁移表型,该表型是对牙齿表面的反应而形成的。由于这些细胞与代谢惰性物质接触,这些变化似乎很大程度上是自我诱导的。该培养方法允许对假定的诱导分子以及可能控制牙-龈界面上皮细胞表型的机制进行研究。

相似文献

1
Changes in cell phenotype during regeneration of junctional epithelium of human gingiva in vitro.人牙龈结合上皮体外再生过程中细胞表型的变化。
J Periodontal Res. 1989 Nov;24(6):370-7. doi: 10.1111/j.1600-0765.1989.tb00885.x.
2
Morphological and functional characteristics of human gingival junctional epithelium.人牙龈结合上皮的形态和功能特征。
BMC Oral Health. 2014 Apr 3;14:30. doi: 10.1186/1472-6831-14-30.
3
Sampling and preliminary analysis of the extra- and intracellular material involved in the attachment of human oral epithelium in vitro.体外人口腔上皮附着过程中细胞外和细胞内物质的取样及初步分析。
J Periodontal Res. 1986 May;21(3):279-87. doi: 10.1111/j.1600-0765.1986.tb01460.x.
4
Transforming growth factor-beta response and expression in junctional and oral gingival epithelial cells.转化生长因子-β在结合上皮和口腔牙龈上皮细胞中的反应与表达。
J Periodontal Res. 1997 Nov;32(8):682-91. doi: 10.1111/j.1600-0765.1997.tb00579.x.
5
Patterns of phenotypic expression of human junctional, gingival and reduced enamel epithelia in vivo and in vitro.人结合上皮、牙龈上皮和缩余釉上皮在体内和体外的表型表达模式。
Epithelial Cell Biol. 1992 Oct;1(4):156-67.
6
Synthesis of type VIII collagen by epithelial cells of human gingiva.人牙龈上皮细胞合成VIII型胶原蛋白。
J Periodontal Res. 1991 Jul;26(4):355-60. doi: 10.1111/j.1600-0765.1991.tb02074.x.
7
Lectin binding patterns in regenerated rat junctional epithelium.再生大鼠结合上皮中的凝集素结合模式
J Osaka Dent Univ. 1994 Dec;28(1-2):17-28.
8
Effect of short chain fatty acids on human gingival epithelial cell keratins in vitro.短链脂肪酸对人牙龈上皮细胞角蛋白的体外作用
Eur J Oral Sci. 2000 Dec;108(6):523-9. doi: 10.1034/j.1600-0722.2000.00881.x.
9
Migration of epithelial cells on materials used in guided tissue regeneration.上皮细胞在引导组织再生所用材料上的迁移。
J Periodontal Res. 1990 Jul;25(4):215-21. doi: 10.1111/j.1600-0765.1990.tb00907.x.
10
Human junctional epithelium: demonstration of a new marker, its growth in vitro and characterization by lectin reactivity and keratin expression.人结合上皮:一种新标志物的证实、其体外生长以及通过凝集素反应性和角蛋白表达进行的特征描述。
J Invest Dermatol. 1991 May;96(5):708-17. doi: 10.1111/1523-1747.ep12470948.

引用本文的文献

1
Histatin 1-modified SIS hydrogels enhance the sealing of peri-implant mucosa to prevent peri-implantitis.组蛋白1修饰的小肠黏膜下层水凝胶增强种植体周围黏膜的封闭性以预防种植体周围炎。
iScience. 2023 Oct 14;26(11):108212. doi: 10.1016/j.isci.2023.108212. eCollection 2023 Nov 17.
2
Smad2 overexpression reduces the proliferation of the junctional epithelium.Smad2 过表达可减少结合上皮的增殖。
J Dent Res. 2014 Sep;93(9):898-903. doi: 10.1177/0022034514543016. Epub 2014 Jul 14.
3
The junctional epithelium originates from the odontogenic epithelium of an erupted tooth.
结合上皮起源于已萌出牙的牙源性上皮。
Sci Rep. 2014 May 2;4:4867. doi: 10.1038/srep04867.
4
Host-bacteria crosstalk at the dentogingival junction.牙-牙龈交界处的宿主-细菌相互作用。
Int J Dent. 2012;2012:821383. doi: 10.1155/2012/821383. Epub 2012 Jul 26.
5
Kindler syndrome and periodontal disease: review of the literature and a 12-year follow-up case.金德勒综合征与牙周病:文献综述及一例12年随访病例
J Periodontol. 2008 May;79(5):961-6. doi: 10.1902/jop.2008.070167.
6
Collagenase-3 (matrix metalloproteinase-13) expression is induced in oral mucosal epithelium during chronic inflammation.在慢性炎症期间,口腔黏膜上皮中会诱导表达胶原酶-3(基质金属蛋白酶-13)。
Am J Pathol. 1998 Jun;152(6):1489-99.
7
Human oral epithelial cell culture I. Improved conditions for reproducible culture in serum-free medium.人口腔上皮细胞培养 I. 无血清培养基中可重复培养的改进条件。
In Vitro Cell Dev Biol. 1990 Jun;26(6):589-95. doi: 10.1007/BF02624208.
8
Human oral epithelial cell culture. II. Keratin expression in fetal and adult gingival cells.人口腔上皮细胞培养。II. 胎儿及成人牙龈细胞中的角蛋白表达
In Vitro Cell Dev Biol. 1990 Jun;26(6):596-603. doi: 10.1007/BF02624209.