DEVELOPMENTAL EXPRESSION AND ANDROGEN REGULATION OF 24 KDA SECRETORY PROTEINS BY THE MURINE EPIDIDYMIS

被引:20
作者
LEFRANCOIS, AM [1 ]
JIMENEZ, C [1 ]
DUFAURE, JP [1 ]
机构
[1] CNRS,URA 360,F-63177 CLERMONT FERRAND,FRANCE
来源
INTERNATIONAL JOURNAL OF ANDROLOGY | 1993年 / 16卷 / 02期
关键词
EPIDIDYMIS; ANDROGEN-DEPENDENT PROTEIN SYNTHESIS; CASTRATION; ORGAN CULTURE;
D O I
10.1111/j.1365-2605.1993.tb01168.x
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Two peptides with a molecular weight of 24 kDa and a P(i) of 8.4-8.8 were found to be synthesized and secreted specifically by the caput epididymis of adult male mice under androgen control. The peptides can interact with spermatozoa. In the present study, the developmental pattern of [S-35]-methionine-labelled proteins synthesized by the murine caput epididymis at 10, 20, 30 and 40 days of age were studied using two-dimensional polyacrylamide gel electrophoresis (2D PAGE) and autoradiography. Active synthesis of the 24 kDa proteins was detected in the epididymis from 20 days of age, but secretion of the two peptides was only observed from 30 days of age onwards. To determine whether androgens influenced the active expression of 24 kDa proteins in the developing epididymis, their effect on [S-35]-methionine incorporation into proteins was assessed using 2D PAGE. Mice were either castrated, castrated then testosterone injected or simply testosterone injected at 10, 20, 30 or 40 days of age. Androgen control of 24 kDa protein expression was also studies in vitro in epididymal organ culture over a 10-day period, with or without testosterone. Androgens were not involved in the initiation of synthesis of the 24 kDa proteins from days 10 to 20, as shown by in-vivo and in-vitro experiments. However, androgens appeared to be essential for maintaining synthesis and secretion of the proteins from 20 days of age onwards. Administration of excessive testosterone was only able to increase secretion of the 24 kDa proteins in intact male mice aged 40 days.
引用
收藏
页码:147 / 154
页数:8
相关论文
共 41 条
[1]   ULTRASTRUCTURE OF THE MOUSE EPIDIDYMAL DUCT WITH SPECIAL REFERENCE TO THE REGIONAL DIFFERENCES OF THE PRINCIPAL CELLS [J].
ABE, K ;
TAKANO, H ;
ITO, T .
ARCHIVUM HISTOLOGICUM JAPONICUM, 1983, 46 (01) :51-68
[2]  
Bedford J. M., 1975, HDB PHYSIOLOGY, P303
[3]   SELECTIVE BINDING OF SPECIFIC RAT EPIDIDYMAL SECRETORY PROTEINS TO SPERMATOZOA AND ERYTHROCYTES [J].
BROOKS, DE .
GAMETE RESEARCH, 1983, 7 (04) :367-376
[4]  
BROOKS DE, 1983, J REPROD FERTIL, V69, P651, DOI 10.1530/jrf.0.0690651
[6]   ANDROGEN-CONTROLLED SPECIFIC PROTEINS IN RAT EPIDIDYMIS [J].
CAMEO, MS ;
GLAQUIER, JA .
JOURNAL OF ENDOCRINOLOGY, 1976, 69 (01) :47-55
[7]   DEVELOPMENTAL ASPECTS OF ANDROGEN-DEPENDENT MESSENGER-RNA FROM RAT VENTRAL PROSTATE USING CLONED CDNA [J].
CARTER, DB ;
YAMADA, K ;
HARRIS, SE .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1983, 31 (2-3) :199-214
[8]   DEVELOPMENTAL EXPRESSION OF AN ANDROGEN-REGULATED EPIDIDYMAL PROTEIN [J].
CHAREST, NJ ;
PETRUSZ, P ;
ORDRONNEAU, P ;
JOSEPH, DR ;
WILSON, EM ;
FRENCH, FS .
ENDOCRINOLOGY, 1989, 125 (02) :942-947
[9]  
COUROT M, 1981, PROG REPRODUCT BIOL, V8, P67
[10]   SEQUENCE OF SPERM CELL-SURFACE DIFFERENTIATION AND ITS RELATIONSHIP TO EXOGENOUS FLUID PROTEINS IN THE RAM EPIDIDYMIS [J].
DACHEUX, JL ;
VOGLMAYR, JK .
BIOLOGY OF REPRODUCTION, 1983, 29 (04) :1033-1046