Since androgens are known to be essential for the completion of spermatogenesis, it is of considerable interest to understand the influences of androgens on testicular cells in molecular terms. Since the Sertoli cells of the seminiferous tubule are thought to play a role in the control of spermatogenic process and we have shown that these cells have androgen receptors, the primary effort of this work will be directed toward defining in biochemical terms androgen-dependent functions of the Sertoli cell and attempting to look at these parameters in the setting of the seminiferous tubule. This proposal also seeks to extend earlier findings on androgen receptor dynamics by using an immunological probe of receptor levels. We will study the effect of androgens on maturational aspects of Sertoli cell function during the first wave of spermatogenesis, including the measurment of newly synthesized cellular and secreted proteins, as detected by 2-dimensional electrophoresis, identified Sertoli cell secretory products or functions, androgen receptor levels, total and poly A+ RNA profiles, translated protein patterns and RNA hybridization to selected cDAN probes. We will attempt to correlate androgen receptor dynamics temporally and quantitatively with selected responses elicited by androgens and to study the effect of other hormones and factors on the responsiveness of the Sertoli cell to androgens. We propose to compare biochemical events accompanying seminiferous tubular development In Vitro with comparable patterns in Sertoli, peritubular and germ cells of corresponding maturity and assess the effect of androgens on these events. We also propose to generate monoclonal antibodies to Sertoli cell androgen receptor for the study of receptor dynamics in the Sertoli cell.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD017795-03
Application #
3314814
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1983-07-01
Project End
1987-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Texas Health Science Center Houston
Department
Type
Schools of Medicine
DUNS #
City
Houston
State
TX
Country
United States
Zip Code
77225
Lu, Q; Porter, L D; Cui, X et al. (2001) Ecto-ATPase mRNA is regulated by FSH in Sertoli cells. J Androl 22:289-301
Walker, W H; Sanborn, B M; Habener, J F (1994) An isoform of transcription factor CREM expressed during spermatogenesis lacks the phosphorylation domain and represses cAMP-induced transcription. Proc Natl Acad Sci U S A 91:12423-7
Ku, C Y; Loose-Mitchell, D S; Sanborn, B M (1994) Both Sertoli and peritubular cells respond to androgens with increased expression of an androgen response element reporter. Biol Reprod 51:319-26
Ku, C Y; Lu, Q; Ussuf, K K et al. (1991) Hormonal regulation of cytochrome oxidase subunit messenger RNAs in rat Sertoli cells. Mol Endocrinol 5:1669-76
Sanborn, B M; Caston, L A; Chang, C et al. (1991) Regulation of androgen receptor mRNA in rat Sertoli and peritubular cells. Biol Reprod 45:634-41
Jakubowiak, A; Janecki, A; Tong, D et al. (1991) Effects of recombinant human inhibin and testosterone on gonadotropin secretion and subunit mRNA in superfused male rat pituitary cell cultures stimulated with pulsatile gonadotropin-releasing hormone. Mol Cell Endocrinol 82:265-73
Buzek, S W; Sanborn, B M (1990) Nuclear androgen receptor dynamics in testicular peritubular and Sertoli cells. J Androl 11:514-20
Caston, L A; Sanborn, B M (1988) Regulation of testicular and Sertoli cell gamma-glutamyl transpeptidase by follicle-stimulating hormone. Biol Reprod 38:109-13
Buzek, S W; Sanborn, B M (1988) Increase in testicular androgen receptor during sexual maturation in the rat. Biol Reprod 39:39-49
Sanborn, B M; Caston, L A; Buzek, S W et al. (1987) Hormonal regulation of Sertoli cell function. Adv Exp Med Biol 219:561-88

Showing the most recent 10 out of 12 publications