LETHAL EFFECT OF THE ANTI-FAS ANTIBODY IN MICE

被引:1794
作者
OGASAWARA, J
WATANABEFUKUNAGA, R
ADACHI, M
MATSUZAWA, A
KASUGAI, T
KITAMURA, Y
ITOH, N
SUDA, T
NAGATA, S
机构
[1] OSAKA BIOSCI INST, 6-2-4 FURUEDAI, SUITA, OSAKA 565, JAPAN
[2] OSAKA CITY INST PUBL HLTH & ENVIRONM SCI, TENNOJI KU, OSAKA 543, JAPAN
[3] UNIV TOKYO, INST MED SCI, LAB ANIM RES CTR, TOKYO 108, JAPAN
[4] OSAKA UNIV, SCH MED, DEPT PATHOL, SUITA, OSAKA 565, JAPAN
关键词
D O I
10.1038/364806a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
DURING mammalian development, many cells are programmed to die1,2 most mediated by apoptosis3. The Fas antigen4 coded by the structural gene for mouse lymphoproliferation mutation (lpr)5,6, is a cell surface protein belonging to the tumour necrosis factor/nerve growth factor receptor family7,8, and mediates apoptosis7. The Fas antigen messenger RNA is expressed in the thymus, liver, heart, lung and ovary8. We prepared a monoclonal antibody against mouse Fas antigen, which immunoprecipitated the antigen (M(r) 45K) and had cytolytic activity against cell lines expressing mouse Fas antigen. We report here that staining of mouse thymocytes with the antibody indicated that thymocytes from the wild-type and lpr(cg) mice expressed the Fas antigen, whereas little expression of the Fas antigen was found in lpr mice. Intraperitoneal administration of the anti-Fas antibody into mice rapidly killed the wild-type mice but neither lpr nor lpr(cg) mice. Biochemical, histological and electron microscope analyses indicated severe damage of the liver by apoptosis. These findings suggest that the Fas antigen is important in programmed cell death in the liver, and may be involved in fulminant hepatitis in some cases.
引用
收藏
页码:806 / 809
页数:4
相关论文
共 27 条
[1]   ABERRANT TRANSCRIPTION CAUSED BY THE INSERTION OF AN EARLY TRANSPOSABLE ELEMENT IN AN INTRON OF THE FAS ANTIGEN GENE OF LPR MICE [J].
ADACHI, M ;
WATANABEFUKUNAGA, R ;
NAGATA, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :1756-1760
[2]   PREFERENTIAL DISTRIBUTION OF APOPTOTIC BODIES IN ACINAR ZONE 3 OF NORMAL HUMAN AND RAT-LIVER [J].
BENEDETTI, A ;
JEZEQUEL, AM ;
ORLANDI, F .
JOURNAL OF HEPATOLOGY, 1988, 7 (03) :319-324
[3]  
Chisari F V, 1992, Mol Genet Med, V2, P67
[4]  
CLIGAN JE, 1991, CURRENT PROTOCOLS IM
[5]   MONOCLONAL-ANTIBODY-MEDIATED APOPTOSIS IN ADULT T-CELL LEUKEMIA [J].
DEBATIN, KM ;
GOLDMANN, CK ;
BAMFORD, R ;
WALDMANN, TA ;
KRAMMER, PH .
LANCET, 1990, 335 (8688) :497-500
[6]   MECHANISMS AND FUNCTIONS OF CELL-DEATH [J].
ELLIS, RE ;
YUAN, JY ;
HORVITZ, HR .
ANNUAL REVIEW OF CELL BIOLOGY, 1991, 7 :663-698
[7]  
ESKANDARI MK, 1992, J IMMUNOL, V148, P2724
[8]  
FALK MH, 1992, BLOOD, V79, P3300
[9]  
HIRATA Y, 1989, J IMMUNOL, V143, P2900
[10]   THE POLYPEPTIDE ENCODED BY THE CDNA FOR HUMAN CELL-SURFACE ANTIGEN FAS CAN MEDIATE APOPTOSIS [J].
ITOH, N ;
YONEHARA, S ;
ISHII, A ;
YONEHARA, M ;
MIZUSHIMA, S ;
SAMESHIMA, M ;
HASE, A ;
SETO, Y ;
NAGATA, S .
CELL, 1991, 66 (02) :233-243