题名 | FGF23(C-tail) improves diabetic nephropathy by attenuating renal fibrosis and inflammation |
作者 | |
发表日期 | 2018-05-30 |
发表期刊 | BMC BIOTECHNOLOGY 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | FGF23 Diabetic nephropathy Inflammation Fibrosis |
其他关键词 | GROWTH-FACTOR 23 ; MOLECULAR-MECHANISMS ; FGF23 ; MORTALITY ; DISEASE ; HYPOPHOSPHATEMIA ; EXPRESSION ; BIOMARKERS ; PHOSPHATE ; INSIGHTS |
摘要 | Background: High level of serum fibroblast growth factor 23 (FGF23) is implicated in the development and progression of diabetic nephropathy (DN), making it a crucial factor in the pathogenesis of DN. FGF23 is also tightly correlated with inflammation in the progression of DN. The aim of this study was to explore whether the C-terminal of FGF23 (FGF23(C-tail)), an antagonist that can block the FGF23 signaling pathway by competing with intact FGF23, could exhibit a therapeutic effect on DN. Results: Biochemical data and histological examination showed that FGF23C-tail administration ameliorated the functional and morphological abnormalities of db/db mice with DN without changing the levels of circulating FGF23 and phosphate. Evaluation of morphology and fibrosis by Masson's trichrome staining and IHC staining of fibronectin, PCR, and western blot analysis showed that FGF23C(-tail) prevents diabetes-induced fibrosis in db/db mice. Importantly, FGF23(C-tail) decreased the levels of inflammatory cytokines in serum and renal tissues. Conclusion: FGF23(C-tail) may improve diabetic nephropathy by decreasing inflammation and fibrosis in db/db mice, suggesting that blocking of FGF23 action remains an important therapeutic target for the prevention or attenuation of the progression of DN. |
资助项目 | Natural Science Foundation of ZhejiangNatural Science Foundation of Zhejiang Province [LY15H300004]; Natural Science Foundation of Zhejiang ProvinceNatural Science Foundation of Zhejiang Province [LQ15H310005]; Science and Technology Project of Wenzhou [Y20140724, Y20140734, Y20160163, Y20170165] |
出版者 | BMC |
出版地 | LONDON |
ISSN | 1472-6750 |
EISSN | 1472-6750 |
卷号 | 18期号:1页码:33 |
DOI | 10.1186/s12896-018-0449-7 |
页数 | 41 |
WOS类目 | Biotechnology & Applied Microbiology |
WOS研究方向 | Biotechnology & Applied Microbiology |
WOS记录号 | WOS:000433586600001 |
收录类别 | SCIE ; PUBMED ; EI ; SCOPUS |
EI入藏号 | 20182205266094 |
EI主题词 | Pathology |
URL | 查看原文 |
PubMed ID | 29843712 |
PMC记录号 | PMC5975516 |
SCOPUSEID | 2-s2.0-85047665776 |
通讯作者地址 | [Huang, Zhifeng]Department of Biopharmacy,School of Pharmacy,Wenzhou Medical University,Chashan Town, Wenzhou,325035,China |
Scopus学科分类 | Biotechnology |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/18718 |
专题 | 药学院(分析测试中心)_生物制药系 |
通讯作者 | Huang, Zhifeng |
作者单位 | Wenzhou Medical University,Department of Biopharmacy,School of Pharmacy,Chashan Town, Wenzhou,325035,China |
第一作者单位 | 温州医科大学 |
通讯作者单位 | 温州医科大学 |
第一作者的第一单位 | 温州医科大学 |
推荐引用方式 GB/T 7714 | Zhang, Xiaomin,Guo, Kaiwen,Xia, Feng,et al. FGF23(C-tail) improves diabetic nephropathy by attenuating renal fibrosis and inflammation[J]. BMC BIOTECHNOLOGY,2018,18(1):33. |
APA | Zhang, Xiaomin, Guo, Kaiwen, Xia, Feng, Zhao, Xinyu, Huang, Zhifeng, & Niu, Jianlou. (2018). FGF23(C-tail) improves diabetic nephropathy by attenuating renal fibrosis and inflammation. BMC BIOTECHNOLOGY, 18(1), 33. |
MLA | Zhang, Xiaomin,et al."FGF23(C-tail) improves diabetic nephropathy by attenuating renal fibrosis and inflammation".BMC BIOTECHNOLOGY 18.1(2018):33. |
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