Apoptosis of hepatic stellate cells in carbon tetrachloride induced acute liver injury of the rat: analysis of isolated hepatic stellate cells

被引:34
作者
Lee, JI
Lee, KS [1 ]
Paik, YH
Park, YN
Han, KH
Chon, CY
Moon, YM
机构
[1] Yonsei Univ, Coll Med, Dept Internal Med, Seoul 120749, South Korea
[2] Yonsei Univ, Coll Med, Dept Pathol, Seoul 120749, South Korea
关键词
hepatic stellate cell; in vivo; ex vivo;
D O I
10.1016/S0168-8278(03)00411-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Analysis of isolated hepatic stellate cells (HSCs) from the injured liver may provide direct information on HSC apoptosis. However, it has not been established whether apoptotic HSCs would be isolated using the usual density gradient centrifugation method. The aim of this study was to observe the serial pattern of proliferation and apoptosis in isolated HSCs in comparison with that of liver tissue sections in CCl4 induced acute liver injury. Methods: Male Sprague-Dawley rats were treated with a single intraperitoneal injection of carbon tetrachloride (CCl4) and were killed at various time points after the treatment. Results: HSC proliferation showed a maximal increase at 32 h after CCl4 injection. Apoptosis of HSC, examined by quantitative analysis of annexin-V-fluorescein isothiocyanate (FITC)staining, showed the maximal increase at 64 h. Apoptosis of HSC in liver tissue sections examined by counting desmin and Tdt-mediated-dUTP biotin nick end labeling (TUNEL) double staining cells, peaked at 64 h. The number of TUNEL positive HSCs in liver tissue sections correlated significantly with annexin-V-FITC binding of isolated HSC. Conclusions: Studying apoptosis using apoptotic HSCs isolated by a usual density gradient centrifugation method from injured tissue sections would be feasible since it correlated with in vivo apoptosis of HSC. (C) 2003 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:960 / 966
页数:7
相关论文
共 35 条
[1]  
ABDELAZIZ G, 1990, AM J PATHOL, V137, P1333
[2]  
ANDREE HAM, 1990, J BIOL CHEM, V265, P4923
[3]   LIPOCYTES FROM NORMAL RAT-LIVER RELEASE A NEUTRAL METALLOPROTEINASE THAT DEGRADES BASEMENT-MEMBRANE (TYPE-IV) COLLAGEN [J].
ARTHUR, MJP ;
FRIEDMAN, SL ;
ROLL, FJ ;
BISSELL, DM .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (04) :1076-1085
[4]   ACTIVATION OF RAT-LIVER PERISINUSOIDAL LIPOCYTES BY TRANSFORMING GROWTH-FACTORS DERIVED FROM MYOFIBROBLASTLIKE CELLS - A POTENTIAL MECHANISM OF SELF PERPETUATION IN LIVER FIBROGENESIS [J].
BACHEM, MG ;
MEYER, D ;
MELCHIOR, R ;
SELL, KM ;
GRESSNER, AM .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (01) :19-27
[5]   MESANGIAL CELL APOPTOSIS - THE MAJOR MECHANISM FOR RESOLUTION OF GLOMERULAR HYPERCELLULARITY IN EXPERIMENTAL MESANGIAL PROLIFERATIVE NEPHRITIS [J].
BAKER, AJ ;
MOONEY, A ;
HUGHES, J ;
LOMBARDI, D ;
JOHNSON, RJ ;
SAVILL, J .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :2105-2116
[6]   p53 in signaling checkpoint arrest or apoptosis [J].
Bates, S ;
Vousden, KH .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (01) :12-18
[7]  
BEDOSSA P, 1994, HEPATOLOGY, V19, P1262, DOI 10.1016/0270-9139(94)90876-1
[8]   OAKLEY,C.L. LECTURE (1993) - CELLULAR AND MOLECULAR ASPECTS OF HEPATIC-FIBROSIS [J].
BURT, AD .
JOURNAL OF PATHOLOGY, 1993, 170 (02) :105-114
[9]  
DeBleser PJ, 1997, HEPATOLOGY, V26, P905
[10]   Expression of the peripheral-type benzodiazepine receptor and apoptosis induction in hepatic stellate cells [J].
Fischer, R ;
Schmitt, M ;
Bode, JG ;
Häussinger, D .
GASTROENTEROLOGY, 2001, 120 (05) :1212-1226