It is believed that, in mature animals, Sertoli cells and jgerm cells of the testis interact to coordinate germ cell differentiation with the biochemical activities and morphological changes, occuring in Sertoli cells, which are necessary for the success of the process of spermatogenesis. Although several models have been proposed for the mechanism of Sertoli-germ cell interaction, as yet no mechanism has been demonstrated to exist. Other workers have suggested that Sertoli cell response to FSH may be modulated by germ cells in vivo. Preliminary evidence from my laboratory shows that germ cells or germ cell membranes can directly stimulate Sertoli membrane adenylate cyclase to an extent comparable with FSH. Taken together, the results suggest the possibilities that Sertoligerm interaction may involve germ cell-dependent modulation of Sertoli response to FSH or may occur by a mechanism identical to the mechanism of peptide hormone action. Therefore, the goal of this proposal is to investigate the hypotheses that germ cells interact with mature Sertoli cells to modify FSH response or that germ cells may directly stimulate Sertoli cell adenylate cyclase to initiate a series of events identical to that initiated by FSH.
The specific aims of the proposal are to determine if germ cells directly or, by modulation of FSH response, indirectly affect Sertoli cell FSH receptor numbers, adenylate cyclase activity, phosphorylation of proteins, cell morphology and distribution of cytoskeletal proteins.
These aims will be approached by using, in a complementary manner, biochemical and morphological techniques applied primarily to an in vitro cell culture experimental model system. It is expected that the proposed research will contribute to our understanding of spermatogenesis and to cell-cell interaction in the testis and may ultimately lead to new avenues of approach to development of male contraceptives. Moreover, this research may reveal a previously unsuspected significance to our appreciation of the mechanism of peptide hormone action, namely that, in order to elicit responses in neighboring cells, cell-cell interaction may involve the same biochemical pathways as those affected by peptide hormones.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD017121-03
Application #
3314187
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1983-01-01
Project End
1986-11-30
Budget Start
1985-01-01
Budget End
1986-11-30
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Hew, K W; Ericson, W A; Welsh, M J (1993) A single low cadmium dose causes failure of spermiation in the rat. Toxicol Appl Pharmacol 121:15-21
Hew, K W; Heath, G L; Jiwa, A H et al. (1993) Cadmium in vivo causes disruption of tight junction-associated microfilaments in rat Sertoli cells. Biol Reprod 49:840-9
Redmond, T; Brott, B K; Jove, R et al. (1992) Localization of the viral and cellular Src kinases to perinuclear vesicles in fibroblasts. Cell Growth Differ 3:567-76
Pittenger, G L; Gilmont, R R; Welsh, M J (1992) The low molecular weight heat shock protein (hsp27) in rat Sertoli cells: evidence for identity of hsp27 with a germ cell-responsive phosphoprotein. Endocrinology 130:3207-15
Welsh, M J; Ireland, M E (1992) The second messenger pathway for germ cell-mediated stimulation of Sertoli cells. Biochem Biophys Res Commun 184:217-24
Van Eldik, L J; Barger, S W; Welsh, M J (1992) Antisense approaches to the function of glial cell proteins. Ann N Y Acad Sci 660:219-30
Sweet, S C; Gnegy, M E; Welsh, M J (1991) Presence of matrix-specific antibodies in affinity-purified polyclonal antibodies. J Immunol Methods 136:31-6
Selinfreund, R H; Barger, S W; Welsh, M J et al. (1990) Antisense inhibition of glial S100 beta production results in alterations in cell morphology, cytoskeletal organization, and cell proliferation. J Cell Biol 111:2021-8
Sanchez, E R; Hirst, M; Scherrer, L C et al. (1990) Hormone-free mouse glucocorticoid receptors overexpressed in Chinese hamster ovary cells are localized to the nucleus and are associated with both hsp70 and hsp90. J Biol Chem 265:20123-30
Redmond, T; Sanchez, E R; Bresnick, E H et al. (1989) Immunofluorescence colocalization of the 90-kDa heat-shock protein and microtubules in interphase and mitotic mammalian cells. Eur J Cell Biol 50:66-75

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