Smad expression of hepatic stellate cells in liver cirrhosis in vivo and hepatic stellate cell line in vitro

被引:40
作者
Kitamura, Y [1 ]
Ninomiya, H
机构
[1] Tottori Univ, Fac Med, Dept Pathol 2, Yonago, Tottori 6838503, Japan
[2] Tottori Univ, Fac Med, Sch Life Sci, Dept Neurobiol, Yonago, Tottori 683, Japan
关键词
cell line; hepatic stellate cell; hepatitis C virus; liver cirrhosis; Smad; transforming growth factor-beta;
D O I
10.1046/j.1440-1827.2003.01431.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Smad expressions, signaling mediators of transforming growth factor-beta (TGF-beta) superfamily of cytokines, were investigated in paraffin-embedded tissue sections of liver cirrhosis due to the hepatitis C virus infection and in the hepatic stellate cell (HSC) line in vitro . Smad 2/3, 4 and 7 was expressed in the nucleus of the HSC in the cirrhotic liver, while the expression was weak in the non-cirrhotic liver. TGF-beta1 expression in the HSC of the cirrhotic liver was strong, while the expression was weak in the non-cirrhotic liver. In situ hybridization also demonstrated the Smad signalings in the HSC of the cirrhotic liver, which confirmed the results of the Smad expressions by immunohistochemistry. The HSC line showed a cytoplasmic and a weak nuclear expression of Smads without TGF-beta1 stimulation, while these cells showed a strong Smad expression in the nucleus by TGF-beta1 stimulation. Immunocytochemical assay demonstrated that the TGF-beta1 stimulation induced the increase of the Smad expressions and the decrease of the autocrine TGF-beta1 in the HSC line. In situ hybridization assay also demonstrated an increase of the Smad mRNA signalings by TGF-beta1 stimulation in vitro . These observations suggest that the Smad expressions increase in the nucleus of the HSC in the cirrhotic liver and that the TGF-beta1 stimulation induces the Smad expression.
引用
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页码:18 / 26
页数:9
相关论文
共 43 条
[1]  
ARTHUR MJP, 1995, J HEPATOL, V22, P43
[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]   OAKLEY,C.L. LECTURE (1993) - CELLULAR AND MOLECULAR ASPECTS OF HEPATIC-FIBROSIS [J].
BURT, AD .
JOURNAL OF PATHOLOGY, 1993, 170 (02) :105-114
[6]   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
[7]  
DELEEUW AM, 1984, HEPATOLOGY, V4, P392
[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]   TGF-beta receptor signaling [J].
Derynck, R ;
Feng, XH .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1997, 1333 (02) :F105-F150
[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