Cellular distribution of EGF, TGF alpha and their receptor during postnatal development and spermatogenesis of the boar testis

被引:35
作者
Caussanel, V
Tabone, E
Mauduit, C
Dacheux, F
Benahmed, M
机构
[1] CTR HOSP LYON SUD, INSERM U407, F-69310 PIERRE BENITE, FRANCE
[2] CTR LEON BERARD, UNITE PATHOL ULTRASTRUCT, F-69373 LYON, FRANCE
[3] PRMD, URA, INRA, CNRS 1291, NOUZILLY, FRANCE
关键词
testis; EGF; TGF alpha; EGF receptor; spermatogenesis; boar;
D O I
10.1016/0303-7207(96)03893-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The epidermal growth factor (EGF), the transforming growth factor alpha (TGF alpha) and the epidermal growth factor receptor (EGFr) have been immunolocalized, (i) during the testicular postnatal development (i.e. at the perinatal, prepubertal and adult periods), and (ii) during the seminiferous epithelium cycle in the different germ cell types. While TGF alpha was essentially observed in somatic cells, specifically in perinatal Leydig cells and in mature Sertoli cells, EGF was localized both in germ cells and in somatic cells with a preferential tubular expression. Furthermore, identification of EGFr in different testicular cell types indicates that during postnatal development and spermatogenesis, testicular cells are potentially responsive to EGF in that they express EGFr. Indeed, in the course of the gonadal development, the EGFr distribution was evidenced both in somatic and germ cells with a specific germ cell pattern depending upon the seminiferous epithelium cycle. A predominant EGFr staining was evidenced during the meiotic process and the spermiogenesis. Together, the present data are in favor of the involvement of the TGF alpha/EGF system in the local control of testicular cells during development and particularly of its potential direct implication in crucial steps of spermatogenesis such as meiosis and spermiogenesis.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 48 条
[1]   NONSTEROIDAL SIGNALS ORIGINATING IN THE GONADS [J].
ACKLAND, JF ;
SCHWARTZ, NB ;
MAYO, KE ;
DODSON, RE .
PHYSIOLOGICAL REVIEWS, 1992, 72 (03) :731-787
[2]  
ASCOLI M, 1987, J BIOL CHEM, V262, P9196
[3]  
ASCOLI M, 1981, J BIOL CHEM, V256, P179
[4]   REGULATION OF INSULIN-LIKE GROWTH FACTOR-I AND STAGE-SPECIFIC LEVELS OF EPIDERMAL GROWTH-FACTOR IN STAGE SYNCHRONIZED RAT TESTES [J].
BARTLETT, JMS ;
SPITERIGRECH, J ;
NIESCHLAG, E .
ENDOCRINOLOGY, 1990, 127 (02) :747-758
[5]  
BENAHMED M, 1996, MALE INFERTILITY, P55
[6]   THE EPIDERMAL GROWTH-FACTOR [J].
BOONSTRA, J ;
RIJKEN, P ;
HUMBEL, B ;
CREMERS, F ;
VERKLEIJ, A ;
HENEGOUWEN, PVE .
CELL BIOLOGY INTERNATIONAL, 1995, 19 (05) :413-430
[7]  
CARPENTER G, 1992, PEPTIDE GROWTH FACTO, P69
[8]   FUNCTIONAL EPIDERMAL GROWTH-FACTOR RECEPTOR LOCALIZES TO THE POSTACROSOMAL REGION OF HUMAN SPERMATOZOA [J].
DAMJANOV, I ;
SOLTER, D ;
KNOWLES, BB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 190 (03) :901-906
[9]   METABOLISM AND EFFECTS OF EPIDERMAL GROWTH-FACTOR AND RELATED GROWTH-FACTORS IN MAMMALS [J].
FISHER, DA ;
LAKSHMANAN, J .
ENDOCRINE REVIEWS, 1990, 11 (03) :418-442
[10]  
FORESTA C, 1994, FERTIL STERIL, V61, P941