题名 | bFGF enhances activation of osteoblast differentiation and osteogenesis on titanium surfaces via PI3K/Akt signaling pathway |
作者 | |
发表日期 | 2016-12-31 |
发表期刊 | INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | Titanium (Ti) osteoblast basic fibroblast growth factor (bFGF) PI3K/Akt signaling pathway |
其他关键词 | BONE MORPHOGENIC PROTEIN-2 ; FIBROBLAST GROWTH-FACTORS ; FGF ; INHIBITION ; RECEPTORS ; IMPLANT ; ROLES ; CELLS ; PROLIFERATION ; MANAGEMENT |
摘要 | Objectives: The aim of this study was to investigate the role of bFGF during the differentiation of osteoblasts and in the course of osteogenesis on titanium surfaces. Materials and methods: Basic f.ibroblast growth factor (bFGF, FGF-2), a member of the fibroblast growth factor family, has many biological effects on cell growth, differentiation, and survival. It was added into this study and MC3T3-E1 Subclone14 was cultivated. The MTT method was used to detect the proliferation of osteoblasts. Alkaline phosphatase (ALP) and osteocalcin (OCN) were examined for indicators of osteoblast differentiation and osteogenesis. Immunofluorescence staining was used to observe protein fluorescence intensity and the Western-blot method was used to analyze the change of the proteins and study the PI3K/Akt signaling pathway. Results: The experimental results showed that the OD values of the MTT, ALP, and OCN rose and the expression levels of OPG, Runx2, and BMP-2 proteins increased when bFGF was added. Moreover, the concentration of 40 ng/ml bFGF was the optimum concentration. Furthermore, the results of signaling pathway analysis indicated that bFGF could promote expression of OPG, Runx2, p-Akt, and BMP-2 proteins via an activated PI3K/Akt signaling pathway. Conclusion: A certain concentration of bFGF could promote the proliferation, differentiation, and osteogenesis of osteoblasts on Ti surfaces via an activated PI3K/Akt signaling pathway. |
资助项目 | National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81000461]; Zhejiang Provincial Natural Science Foundation of ChinaNatural Science Foundation of Zhejiang Province [Y2100274]; Wenzhou Science and Technology Bureau projects [Y20140699] |
出版者 | E-CENTURY PUBLISHING CORP |
出版地 | MADISON |
ISSN | 1936-2625 |
卷号 | 9期号:4页码:4680-4692 |
页数 | 13 |
WOS类目 | Oncology ; Pathology |
WOS研究方向 | Oncology ; Pathology |
WOS记录号 | WOS:000377601900047 |
收录类别 | SCIE ; SCOPUS |
URL | 查看原文 |
SCOPUSEID | 2-s2.0-84969506763 |
通讯作者地址 | [Ding, Xi]Department of Stomatology,The First Affiliated Hospital,Wenzhou Medical University,Nanbaixiang, Ouhai District, Wenzhou, Zhejiang,325000,China |
Scopus学科分类 | Pathology and Forensic Medicine;Histology |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/12710 |
专题 | 药学院(分析测试中心)_生物制药系_生物制药工程 附属第一医院 研究生工作部(研究生院) 口腔医学院、附属口腔医院_儿童口腔 |
通讯作者 | Ding, Xi |
作者单位 | 1.Department of Stomatology,The First Affiliated Hospital,Wenzhou Medical University,Wenzhou, Zhejiang,China; 2.Department of Pediatric Dentistry,School and Hospital of Stomatology,Wenzhou Medical University,Wenzhou, Zhejiang,China; 3.School of Pharmacy,Key Laboratory of Biotechnology and Pharmaceutical Engineering,Wenzhou Medical University,Wenzhou, Zhejiang,China |
第一作者单位 | 附属第一医院; 口腔医学院、附属口腔医院 |
通讯作者单位 | 附属第一医院 |
第一作者的第一单位 | 附属第一医院 |
推荐引用方式 GB/T 7714 | Zheng, An-Qi,Xiao, Jian,Xie, Jing,et al. bFGF enhances activation of osteoblast differentiation and osteogenesis on titanium surfaces via PI3K/Akt signaling pathway[J]. INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY,2016,9(4):4680-4692. |
APA | Zheng, An-Qi, Xiao, Jian, Xie, Jing, Lu, Pei-Pei, & Ding, Xi. (2016). bFGF enhances activation of osteoblast differentiation and osteogenesis on titanium surfaces via PI3K/Akt signaling pathway. INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 9(4), 4680-4692. |
MLA | Zheng, An-Qi,et al."bFGF enhances activation of osteoblast differentiation and osteogenesis on titanium surfaces via PI3K/Akt signaling pathway".INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY 9.4(2016):4680-4692. |
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