Expression of Fas system-related genes in the testis during development and after toxicant exposure

被引:37
作者
Boekelheide, K [1 ]
Lee, J [1 ]
Shipp, EB [1 ]
Richburg, JH [1 ]
Li, G [1 ]
机构
[1] Brown Univ, Dept Pathol & Lab Med, Providence, RI 02912 USA
关键词
testis; apoptosis; Sertoli cell; germ cell; Fas system;
D O I
10.1016/S0378-4274(98)00242-2
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The Fas system has been identified as a key regulator of testicular germ cell apoptosis. The goal of these experiments was to explore the expression of Fas system-related genes in the testis during development and after toxicant exposure. Both Fas ligand (FasL) and Fas receptor (Fas) were expressed postnatally in rat testis with peak expression associated with the high levels of germ cell apoptosis found during the first wave of spermatogenesis. The testicular expression of RIP and FAP-1, components of the Pas activating complex, increased after exposure to mono-(2-ethylhexyl)phthalate (MEHP), a Sertoli cell toxicant which induces massive germ cell death. Finally, the expression of additional apoptosis-inducing genes, including tumor necrosis factor receptor (TNFR), FADD, TRAIL, and DR5, was detected in mammalian testis. These results provide additional support for the following concepts: (1) Sertoli-germ cell interactions are important in the control of germ cell apoptosis; and (2) the Fas system and similar paracrine systems are important modulators of testicular homeostasis. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:503 / 508
页数:6
相关论文
共 24 条
[1]   SPERMATOGONIAL APOPTOSIS HAS 3 MORPHOLOGICALLY RECOGNIZABLE PHASES AND SHOWS NO CIRCADIAN-RHYTHM DURING NORMAL SPERMATOGENESIS IN THE RAT [J].
ALLAN, DJ ;
HARMON, BV ;
ROBERTS, SA .
CELL PROLIFERATION, 1992, 25 (03) :241-250
[2]   APOPTOSIS OF MALE GERM-CELLS, A GENERALIZED OR A CELL-TYPE-SPECIFIC PHENOMENON [J].
BARTKE, A .
ENDOCRINOLOGY, 1995, 136 (01) :3-4
[3]   APOPTOSIS IN TESTIS GERM-CELLS - DEVELOPMENTAL-CHANGES IN GONADOTROPIN DEPENDENCE AND LOCALIZATION TO SELECTIVE TUBULE STAGES [J].
BILLIG, H ;
FURUTA, I ;
RIVIER, C ;
TAPANAINEN, J ;
PARVINEN, M ;
HSUEH, AJW .
ENDOCRINOLOGY, 1995, 136 (01) :5-12
[4]   Fate of germ cells in 2,5-hexanedione-induced testicular injury .1. Apoptosis is the mechanism of germ cell death [J].
Blanchard, KT ;
Allard, EK ;
Boekelheide, K .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1996, 137 (02) :141-148
[5]   FADD, A NOVEL DEATH DOMAIN-CONTAINING PROTEIN, INTERACTS WITH THE DEATH DOMAIN OF FAS AND INITIATES APOPTOSIS [J].
CHINNAIYAN, AM ;
OROURKE, K ;
TEWARI, M ;
DIXIT, VM .
CELL, 1995, 81 (04) :505-512
[6]   A FAS-ASSOCIATED PROTEIN FACTOR, FAF1, POTENTIATES FAS-MEDIATED APOPTOSIS [J].
CHU, KT ;
NIU, XH ;
WILLIAMS, LT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11894-11898
[7]  
Furuchi T, 1996, DEVELOPMENT, V122, P1703
[8]   Radiation-induced cell death in the mouse testis: Relationship to apoptosis [J].
Hasegawa, M ;
Wilson, G ;
Russell, LD ;
Meistrich, ML .
RADIATION RESEARCH, 1997, 147 (04) :457-467
[9]   Resistance of differentiating spermatogonia to radiation-induced apoptosis and loss in p53-deficient mice [J].
Hasegawa, M ;
Zhang, Y ;
Niibe, H ;
Terry, NHA ;
Meistrich, ML .
RADIATION RESEARCH, 1998, 149 (03) :263-270
[10]   MORPHOLOGY AND KINETICS OF SPERMATOGONIAL DEGENERATION IN NORMAL ADULT RATS - ANALYSIS USING A SIMPLIFIED CLASSIFICATION OF GERMINAL EPITHELIUM [J].
HUCKINS, C .
ANATOMICAL RECORD, 1978, 190 (04) :905-926