首页 | 本学科首页   官方微博 | 高级检索  
     

下颌骨骨折愈合过程中整合素β_1mRNA表达的实验研究
引用本文:李声伟 刘少华 等. 下颌骨骨折愈合过程中整合素β_1mRNA表达的实验研究[J]. 华西口腔医学杂志, 2001, 19(6): 351-353
作者姓名:李声伟 刘少华 等
作者单位:610041 四川大学华西口腔医学院
摘    要:目的:探讨下颌骨骨折愈合过程中整合素B1mRNA时空表达的变化。方法:用地高辛标记的整合素B1mRNA 的寡核苷酸探针,采用组织切片原位杂交技术,观察下颌骨骨折愈合过程中整合素B1mRNA的时空表达变化。结果:骨折愈合过程中,整合素B1mRNA在骨组织细胞,特别是成骨细胞中广泛表达;阳性染色出现于细胞浆和细胞核中;骨组织中的整合素B1mRNA在骨折7 d后表达增强,14至30 d最强,60至90 d时基本接近正常。结论:下颌骨骨折的愈合过程中,骨组织细胞中整合素B1mRNA表达增强,提示整合素B1对骨折的愈合过程具有重要作用。

关 键 词:整合素β1mRNA  骨折愈合  原位杂交  
收稿时间:2001-12-25
修稿时间:2001-07-13

A Study on mRNA Expression Levels of Integrin
S Li,S Liu,W Tian,G Cheng,L Liu. A Study on mRNA Expression Levels of Integrin[J]. West China journal of stomatology, 2001, 19(6): 351-353
Authors:S Li  S Liu  W Tian  G Cheng  L Liu
Affiliation:College of Stomatology, West China University of MedicalSciences
Abstract:OBJECTIVE: The aim of this study was to investigate the spatial and temporal mRNA expression changes of integrin beta 1 during the healing process of mandibular fractures. METHODS: The in situ hybridization was performed using digoxigenin-labeled integrin beta 1 mRNA oligonucleotide probe. During the healing process of mandibular fractures, the staining pattern of beta 1 mRNA was examined both spatially and time-dependently. RESULTS: Integrin beta 1 was widely present in the cells of the fractured bone, especially in osteoblasts. The positive staining was observed in the cytoplasm and nucleolus of osteoblasts. After 7 days of fracture, the expression level of integrin beta 1 increased. The peak appeared between the 14th and the 30th day, and almost recovered to normal between the 60th and 90th day. CONCLUSION: During the healing process of mandibular fracture, the expression level of integrin beta 1 in bone, especially in osteoblasts rose. It is suggested that integrin beta 1 may play an important role in the fracture healing process.
Keywords:integrinB1  message RNA  fracture healing  in situ hybridization  
本文献已被 维普 等数据库收录!
点击此处可从《华西口腔医学杂志》浏览原始摘要信息
点击此处可从《华西口腔医学杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号