题名 | BMP-7 attenuates liver fibrosis via regulation of epidermal growth factor receptor |
作者 | |
发表日期 | 2014-12-31 |
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 | Carbon tetrachloride liver fibrosis bone morphogenetic protein-7 epidermal growth factor receptor hepatic stellate cell liver fibrosis. |
其他关键词 | BONE-FORMATION ; FACTOR-BETA ; DEFECTS ; TRANSITION ; MECHANISMS ; MICE |
摘要 | The aim of this study was to elucidate the effect of bone morphogenetic protein-7 (BMP-7) on liver fibrosis induced by carbon tetrachloride (CCl4) in vivo and on the hepatic stellate cells (HSC) activation in vitro. In vivo, thirty male ICR mice were randomly allocated to three groups, the control group (n = 6), the CCl4 group (n = 18) and the BMP-7+CCl4 group (n = 6). The model of liver fibrosis was induced by intraperitoneal injection with CCl4 three times per week lasting for 12 weeks in CCl4 group and the BMP-7+CCl4 group. After 8 weeks injection with CCl4, mice were intraperitoneal injected with human recombinant BMP-7 in BMP-7+CCl4 group. Meanwhile, mice in the CCl4 group were only intraperitoneal injection with equal amount of saline. The degree of liver fibrosis was assessed by HE and Masson's staining. PCR and western blot were used to detect mRNA and protein levels. In BMP-7+CCl4 group, serum levels of alanine aminotransferase (ALT) and aminotransferase (AST) were decreased and serum albumin (Alb) was increased. Meanwhile, the expressions of transforming growth factor-beta 1 (TGF-beta 1) and alpha-smooth muscle actin (alpha-SMA) were down-regulated by BMP-7 intervention as compared to the CCl4 group (P < 0.05). Furthermore, BMP-7 also suppressed the expression of epidermal growth factor receptor (EGFR) and phosphorylated-epidermal growth factor receptor (pEGFR). HE and Masson stain showed that liver damage was alleviated in BMP-7+CCl4 group. In vitro study, expression of EGFR, TGF-beta 1 and alpha-SMA were down regulated by BMP-7 dose-dependently, indicating it might effect on suppression of HSC activation. Therefore, our data indicate BMP-7 was capable of inhibiting liver fibrosis and suppressing HSCs activation, and these effects might rely on its crosstalk with EGFR and TGF-beta 1. We suggest that BMP-7 may be a potential reagentfor the prevention and treatment of liver fibrosis. |
资助项目 | Zhejiang Provincial Natural Science Foundation of ChinaNatural Science Foundation of Zhejiang Province [2013ZX10005002-001] |
出版者 | E-CENTURY PUBLISHING CORP |
出版地 | MADISON |
ISSN | 1936-2625 |
卷号 | 7期号:7页码:3537-3547 |
页数 | 11 |
WOS类目 | Oncology ; Pathology |
WOS研究方向 | Oncology ; Pathology |
WOS记录号 | WOS:000341264400004 |
收录类别 | SCIE ; SCOPUS ; PUBMED |
URL | 查看原文 |
PubMed ID | 25120732 |
PMC记录号 | PMC4128967 |
SCOPUSEID | 2-s2.0-84906248961 |
通讯作者地址 | [Chen, Yong-Ping]Department of Infection and Liver Diseases, Liver Research Center, The First Affiliated Hospital of Wenzhou Medical University,Nanbaixiang Street,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/15232 |
专题 | 附属第一医院 |
通讯作者 | Chen, Yong-Ping |
作者单位 | 1.Department of Infection Disease, The First Affiliated Hospital of Wenzhou Medical University,China; 2.Department of Pulmonary Medicine, Fuzhou Pulmonary Hospital of Fujian,China |
第一作者单位 | 附属第一医院 |
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 | Wang, Li-Ping,Dong, Jin-Zhong,Xiong, Li-Jun,et al. BMP-7 attenuates liver fibrosis via regulation of epidermal growth factor receptor[J]. INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY,2014,7(7):3537-3547. |
APA | Wang, Li-Ping., Dong, Jin-Zhong., Xiong, Li-Jun., Shi, Ke-Qing., Zou, Zhuo-Lin., ... & Chen, Yong-Ping. (2014). BMP-7 attenuates liver fibrosis via regulation of epidermal growth factor receptor. INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 7(7), 3537-3547. |
MLA | Wang, Li-Ping,et al."BMP-7 attenuates liver fibrosis via regulation of epidermal growth factor receptor".INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY 7.7(2014):3537-3547. |
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