The primary goals of this application are to elucidate mechanisms of maturation of spermatozoa in the epididymis which will lead to an understanding of how fertility is regulated in the male. Maturation of sperm in the epididymis involves interactions among sperm, luminal fluid, and the epididymal epithelium (which is regulated by factors from the blood vascular system). In the experiments to be done in this application, investigation will be undertaken on proteins which are synthesized and secreted by the epididymal epithelium. Antibodies raised against these proteins cross-react with molecules on the sperm surface as well as with molecules that are derived from the testis.
The first aim of this grant proposal is to isolate pure compounds from rete testis fluid, from the epididymis, and from sperm surfaces, which will then be studied extensively with respect to their amino acid sequences and the carbohydrate components of their oligosaccharide chains. The underlying theme of these experiments is to determine whether all of the molecules that cross-react immunologically are actually structurally the same, and whether they are the same as the Alpha-lactalbumin from rat milk. After deducing their structure, the molecules will be studied with respect to their ability to modify galactosyltransferase activity, which is a major function of Alpha-lactalbumin.
The third aim i n the project is related to studies on the synthesis and secretion (and control of these two functions) of immunologically cross-reactive molecules from the epididymis in culture. We have developed a perifusion culture system for epididymal tubules that will allow us to do studies on long-term cultures of epididymis, in which we know that epididymal epithelium and sperm are reasonably normal. Finally, using the well characterized monoclonal antibodies raised against the individual polypeptides of the epididymal Alpha-lactalbumin complex, experiments will be done to determine whether the molecules have any effect on sperm motility or fertilizing ability.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD011962-08
Application #
3311733
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1978-09-29
Project End
1988-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
8
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Liu, Mian; Hamilton, David W; Barany, George (2010) Solid-phase synthesis and evaluation of glycopeptide fragments from rat epididymal cysteine-rich secretory protein-1 (Crisp-1). Molecules 15:6399-410
Roberts, Kenneth P; Ensrud-Bowlin, Kathy M; Piehl, Laura B et al. (2008) Association of the protein D and protein E forms of rat CRISP1 with epididymal sperm. Biol Reprod 79:1046-53
Roberts, Kenneth P; Johnston, Daniel S; Nolan, Michael A et al. (2007) Structure and function of epididymal protein cysteine-rich secretory protein-1. Asian J Androl 9:508-14
Roberts, Kenneth P; Wamstad, Joseph A; Ensrud, Kathy M et al. (2003) Inhibition of capacitation-associated tyrosine phosphorylation signaling in rat sperm by epididymal protein Crisp-1. Biol Reprod 69:572-81
Roberts, Kenneth P; Ensrud, Kathy M; Hamilton, David W (2002) A comparative analysis of expression and processing of the rat epididymal fluid and sperm-bound forms of proteins D and E. Biol Reprod 67:525-33
Roberts, K P; Hoffman, L B; Ensrud, K M et al. (2001) Expression of crisp-1 mRNA splice variants in the rat epididymis, and comparative analysis of the rat and mouse crisp-1 gene regulatory regions. J Androl 22:157-63
Klemme, L M; Roberts, K P; Hoffman, L B et al. (1999) Cloning and characterization of the rat Crisp-1 gene. Gene 240:279-88
Xu, W; Ensrud, K M; Hamilton, D W (1997) The 26 kD protein recognized on rat cauda epididymal sperm by monoclonal antibody 4E9 has internal peptide sequence that is identical to the secreted form of epididymal protein E. Mol Reprod Dev 46:377-82
Xu, W; Hamilton, D W (1996) Identification of the rat epididymis-secreted 4E9 antigen as protein E: further biochemical characterization of the highly homologous epididymal secretory proteins D and E. Mol Reprod Dev 43:347-57
Siiteri, J E; Ensrud, K M; Moore, A et al. (1995) Identification of osteopontin (OPN) mRNA and protein in the rat testis and epididymis, and on sperm. Mol Reprod Dev 40:16-28

Showing the most recent 10 out of 24 publications