Connective tissue growth factor (CTGF/CCN2) in hepatic fibrosis

被引:243
作者
Rachfal, AW
Brigstock, DR [1 ]
机构
[1] Ohio State Univ, Dept Surg, Columbus, OH 43212 USA
[2] Ohio State Univ, Dept Mol & Cellular Biochem, Columbus, OH 43212 USA
[3] Ohio State Univ, Mol Cellular & Dev Biol Program, Columbus, OH 43212 USA
[4] Childrens Res Inst, Ctr Cell & Vasc Biol, Columbus, OH 43205 USA
基金
美国国家卫生研究院;
关键词
CTGF/CCN2; TGF-beta; hepatic stellate cell; extracellular matrix; matricellular; CCN;
D O I
10.1016/S1386-6346(03)00115-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Connective tissue growth factor (CTGF/CCN2) is a highly profibrogenic molecule which is overexpressed in many fibrotic lesions, including those of the liver. CTGF/CCN2 is transcriptionally activated by transforming growth factor-beta (TGF-beta) and appears to mediate some of the extracellular matrix (ECM)-inducing properties that have been previously attributed to TGF-beta. CTGF/CCN2 and TGF-beta stimulate connective tissue cell proliferation and ECM synthesis in vitro and exhibit shared fibrogenic and angiogenic properties in vivo. In fibrotic liver, CTGF/CCN2 mRNA and protein are produced by fibroblasts, myofibroblasts, hepatic stellate cells (HSCs), endothelial cells, and bile duct epithelial cells. CTGF/CCN2 is also produced at high levels in hepatocytes during cytochrome P-4502E1-mediated ethanol oxidation. CTGF/CCN2 expression in cultured HSCs is enhanced following their activation or stimulation by TGF-beta while exogenous CTGF/CCN2 is able to promote HSC adhesion, proliferation, locomotion, and collagen production. Collectively, these data suggest that during initiating or downstream fibrogenic events in the liver, production of CTGF/CCN2 is regulated primarily by TGF-beta in one or more cell types and that CTGF/CCN2 plays important roles in HSC activation and progression of fibrosis. This article reviews the data that support the importance of CTGF/CCN2 in hepatic fibrosis and highlights the concept that CTGF/CCN2 may represent a new therapeutic target in this disease. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 106 条
[1]   Connective tissue growth factor in human liver cirrhosis [J].
Abou-Shady, M ;
Friess, H ;
Zimmermann, A ;
di Mola, FF ;
Guo, XZ ;
Baer, HU ;
Büchler, MW .
LIVER, 2000, 20 (04) :296-304
[2]   Enhanced insulin-like growth factor finding protein-related protein 2 (connective tissue growth factor) expression in patients with idiopathic pulmonary fibrosis and pulmonary sarcoidosis [J].
Allen, JT ;
Knight, RA ;
Bloor, CA ;
Spiteri, MA .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 21 (06) :693-700
[3]   COMPLEXITY OF THE EARLY GENETIC RESPONSE TO GROWTH-FACTORS IN MOUSE FIBROBLASTS [J].
ALMENDRAL, JM ;
SOMMER, D ;
MACDONALDBRAVO, H ;
BURCKHARDT, J ;
PERERA, J ;
BRAVO, R .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2140-2148
[4]   REGULATION OF TGF-BETA GENE-EXPRESSION IN RAT-LIVER INTOXICATED WITH CARBON-TETRACHLORIDE [J].
ARMENDARIZBORUNDA, J ;
SEYER, JM ;
KANG, AH ;
RAGHOW, R .
FASEB JOURNAL, 1990, 4 (02) :215-221
[5]   Establishment of a recombinant expression system for connective tissue growth factor (CTGF) that models CTGF processing in utero [J].
Ball, DK ;
Moussad, EEDA ;
Rageh, MAE ;
Kemper, SA ;
Brigstock, DR .
REPRODUCTION, 2003, 125 (02) :271-284
[6]   The heparin-binding 10 kDa fragment of connective tissue growth factor (CTGF) containing module 4 alone stimulates cell adhesion [J].
Ball, DK ;
Rachfal, AW ;
Kemper, SA ;
Brigstock, DR .
JOURNAL OF ENDOCRINOLOGY, 2003, 176 (02) :R1-R7
[7]   Transforming growth factor-β1 in autoimmune hepatitis:: correlation of liver tissue expression and serum levels with disease activity [J].
Bayer, EM ;
Herr, W ;
Kanzler, S ;
Waldmann, C ;
Zum Büschenfelde, KHM ;
Dienes, HP ;
Lohse, AW .
JOURNAL OF HEPATOLOGY, 1998, 28 (05) :803-811
[8]   Gene regulation of connective tissue growth factor: new targets for antifibrotic therapy [J].
Blom, IE ;
Goldschmeding, R ;
Leask, A .
MATRIX BIOLOGY, 2002, 21 (06) :473-482
[9]   SUPPRESSION OF EXPERIMENTAL GLOMERULONEPHRITIS BY ANTISERUM AGAINST TRANSFORMING GROWTH FACTOR-BETA-1 [J].
BORDER, WA ;
OKUDA, S ;
LANGUINO, LR ;
SPORN, MB ;
RUOSLAHTI, E .
NATURE, 1990, 346 (6282) :371-374
[10]   NATURAL INHIBITOR OF TRANSFORMING GROWTH-FACTOR-BETA PROTECTS AGAINST SCARRING IN EXPERIMENTAL KIDNEY-DISEASE [J].
BORDER, WA ;
NOBLE, NA ;
YAMAMOTO, T ;
HARPER, JR ;
YAMAGUCHI, Y ;
PIERSCHBACHER, MD ;
RUOSLAHTI, E .
NATURE, 1992, 360 (6402) :361-364