Expression and location of Smad2, 4 mRNAs during and after liver fibrogenesis of rats

被引:24
作者
Liu, Yang
Wang, Li-Feng
Zou, Hai-Feng
Song, Xiao-Yan
Xu, Hua-Feng
Lin, Ping
Zheng, Hai-Hong
Yu, Xiao-Guang [1 ]
机构
[1] Harbin Med Univ, Dept Biochem & Mol Biol, Harbin 150086, Heilongjiang Pr, Peoples R China
[2] Harbin Med Univ, Dept Pathol, Harbin 150001, Heilongjiang Pr, Peoples R China
[3] Harbin Med Univ, Clin Coll 1, Harbin 150001, Heilongjiang Pr, Peoples R China
[4] Harbin Med Univ, Dept Pathol, Harbin 150086, Heilongjiang Pr, Peoples R China
[5] Harbin Med Univ, Clin Coll 2, Dept Expt Anim, Harbin 150086, Heilongjiang Pr, Peoples R China
关键词
Smad2; Smad4; mRNA; liver fibrogenesis;
D O I
10.3748/wjg.v12.i10.1577
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the location alteration of Smad2 and Smad4 mRNAs in the liver during and after fibrogenesis in rats. METHODS: Eighty, male Wistar rats weighing approximately 200 g each were used. The rat models of experimental hepatic fibrosis were established by injection with carbon tetrachloride (CCl4), normal rats and rats were injected with olive oil and served as control groups. In situ hybridization(ISH) was used to detect the Smad2 and Smad4 mRNA in liver. RESULTS: In situ hybridization showed Smad2 and Smad4 mRNA expressions in the cytoplasm of hepatic stellate cells (HSC), fibroblasts and myofibroblasts around the central vein and hepatic sinus during and after fibrogenesis. Expression of Smad2, 4 mRNA was higher than that in normal and control rats. CONCLUSION: In the process of and after hepatic fibrosis formation, HSC, fibroblasts and myofibroblasts are the major cells that express Smad2 and Smad4. The more serious the hepatic fibrosis is in the injured liver, the higher the level of Smad2 and Smad4 gene expression is during and after fibrogenesis respectively. (C) 2006 The WJG Press. All rights reserved.
引用
收藏
页码:1577 / 1582
页数:6
相关论文
共 31 条
[1]
Extracellular matrix degradation and the role of hepatic stellate cells [J].
Benyon, RC ;
Arthur, MJP .
SEMINARS IN LIVER DISEASE, 2001, 21 (03) :373-384
[2]
CELL-SPECIFIC EXPRESSION OF TRANSFORMING GROWTH-FACTOR-BETA IN RAT-LIVER - EVIDENCE FOR AUTOCRINE REGULATION OF HEPATOCYTE PROLIFERATION [J].
BISSELL, DM ;
WANG, SS ;
JARNAGIN, WR ;
ROLL, FJ .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (01) :447-455
[3]
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
[4]
BORDER WA, 1994, NEW ENGL J MED, V331, P1286
[5]
Cell adhesion molecules involved in invasion of renal carcinoma cells into the extracellular matrix [J].
Brenner, W ;
Gross, S ;
Steinbach, F ;
Horn, S ;
Hohenfellner, R ;
Thüroff, JW .
AKTUELLE UROLOGIE, 2001, 32 (01) :32-37
[7]
REGULATION OF EXTRACELLULAR-MATRIX SYNTHESIS BY TRANSFORMING GROWTH FACTOR-BETA(1) IN HUMAN FAT-STORING CELLS [J].
CASINI, A ;
PINZANI, M ;
MILANI, S ;
GRAPPONE, C ;
GALLI, G ;
JEZEQUEL, AM ;
SCHUPPAN, D ;
ROTELLA, CM ;
SURRENTI, C .
GASTROENTEROLOGY, 1993, 105 (01) :245-253
[8]
Nomenclature: Vertebrate mediators of TGF beta family signals [J].
Derynck, R ;
Gelbart, WM ;
Harland, RM ;
Heldin, CH ;
Kern, SE ;
Massague, J ;
Melton, DA ;
Mlodzik, MB ;
Padgett, RW ;
Roberts, AB ;
Smith, J ;
Thomsen, GH ;
Vogelstein, B ;
Wang, XF .
CELL, 1996, 87 (02) :173-173
[9]
DERYNCK R, 1997, BIOCHIM BIOPHYS ACTA, V1333, P105
[10]
Modulation of transforming growth factor β response and signaling during transdifferentiation of rat hepatic stellate cells to myofibroblasts [J].
Dooley, S ;
Delvoux, B ;
Lahme, B ;
Mangasser-Stephan, K ;
Gressner, AM .
HEPATOLOGY, 2000, 31 (05) :1094-1106