华西口腔医学杂志

• 专栏论著 • 上一篇    下一篇

阻遏蛋白β-TrCP在小鼠牙胚不同发育时期的表达与意义

沈永岱;田卫东;刘磊;何永红;汤炜;郑晓辉   

  1. 口腔生物医学工程教育部重点实验室, 四川大学, 四川成都610041
  • 收稿日期:2007-04-25 修回日期:2007-04-25 出版日期:2007-04-20 发布日期:2007-04-20
  • 通讯作者: 田卫东,Tel:028- 85503406
  • 作者简介:沈永岱(1966-),男,甘肃人,主治医师,博士研究生
  • 基金资助:

    国家自然科学基金资助项目(30471904和30572051);教育部重点资助项目(106134)

β- tr ansduction Repeat Containing Protein Expr essed in Tooth Germs and Ameloblast and Odontoblast of Differ ent Stage of Tooth Development

SHEN Yong- dai, TIAN Wei- dong, LIU Lei, HE Yong- hong, TANG Wei, ZHENG Xiao- hui   

  1. Key. Laboratory of Oral Biomedical Engineering of Ministry of Education, Sichuan University, Chengdu 610041, China
  • Received:2007-04-25 Revised:2007-04-25 Online:2007-04-20 Published:2007-04-20
  • Contact: TIAN Wei- dong,Tel:028- 85503406

摘要:

目的观察Sonic hedgehog(shh)信号转导通路的阻遏蛋白β- TrCP在小鼠牙胚发育不同时期的表达情况,探讨β- TrCP在晚期牙胚发育中的作用与意义。方法取不同发育时期的鼠胚、乳鼠鼠头标本,用标记生物素链亲和素LsAB法观察β- TrCP蛋白在不同发育时期牙胚组织的表达情况。结果β- TrCP在胚胎10.5、13.5、14.5、16.5、18.5 d的小鼠牙胚上皮层与间充质层,以及出生后0、3、6 d的小鼠成釉细胞与成牙本质细胞胞浆呈特征性表达。结论β- TrCP在正常发育小鼠牙胚及成釉细胞与成牙本质细胞特征性表达,提示β- TrCP在牙胚发育中维持/限定shh信号通路的正常信号转导具有重要意义。

关键词: 牙胚, 成釉细胞, 成牙本质细胞

Abstract:

Objective The Sonic hedgehog signalling peptide has been demonstrated to play important roles in the growth and patterning of the tooth development. This study aims on whether the antagonist β- transduction repeat containing protein of Sonic hedgehog signal transduction expressed in tooth germs ameloblast and odontoblast or not. Methods The mouse embryo heads of different developmental stages of E10.5, E13.5, E14.5, E16.5, E18.5 and P0, P3, P6 after birth were acquired fixed with 4% paraformaldehyde for 48 hours, embeded with Paraffin and examined using LsAB(labelled streptavidin- biotin)method to observe the β- TrCP expression pattern in tooth germs, ameloblast and odontoblast. Results It was demonstrated that β- TrCP expressed in oral epithelium, tooth bud, mesenchymal cell cytoplasm of ameloblast and odontoblast of different stage of tooth development. Conclusion β- TrCP expressed from early stage to later stage of murine tooth development. And these findings provide the evidence of antagonist regulatory pathways for shh in teeth development.

Key words: tooth germs, ameloblast, odontoblast