Objectives To determine the role of an oviductal glycoprotein, oviductin, or estrogen-dependent glycoprotein, in fertilization. ABSTRACT:Oviductin is a glycoprotein present in oviductal secretions during the periovulatory and early embryonic development periods. In the primate, synthesis and secretion of oviductin is coordinated with the reproductive cycle, being up- regulated by estradiol and down-regulated by progesterone. Oviductins belong to a newly discovered class of mammalian proteins that share homology with chitinases but have no chitinase enzymic activity. For preliminary work (to be confirmed eventually in primates), the function of oviductin has been assayed using a golden hamster fertilization system. This model animal system was chosen because ova are abundant and both ovulated and non-ovulated mature ova can be obtained; early stages of sperm penetration and fertilization are easily assessed; and the large size of the sperm!s head permits regional localization of markers at the light microscopic level. As visualized by indirect immunofluorescence, affinity purified hamster oviductin binds to the zona pellucida of hamster eggs and to the sperm!s head, with regional localization of binding to sperm changing during sperm capacitation. Oviductin binds to sperm both in vitro and in vivo (determined in sperm flushed from oviducts of mated animals). Oviductin profoundly increases the speed of sperm penetration through the zona pellucida the mechanism for this action appears to occur by increased adhesiveness of acrosome reacting sperm for the zona pellucida. Oviductins are heavily glycosylated, with marked variations occurring between species. As determined by probes of transblots with biotinylated lectins, hamster oviductin is strongly positive for N-acetyl-D-glucosamine and alpha-linked-N-acetyl-D-galactosamine, and weakly reactive for alpha-mannose. These preliminary findings in the golden hamster form a strong basis for future highly directed studies of oviductin!s function in primate fertilization and early embryonic development.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000167-36
Application #
3718931
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
36
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Kang, HyunJun; Mesquitta, Walatta-Tseyon; Jung, Ho Sun et al. (2018) GATA2 Is Dispensable for Specification of Hemogenic Endothelium but Promotes Endothelial-to-Hematopoietic Transition. Stem Cell Reports 11:197-211
Rhoads, Timothy W; Burhans, Maggie S; Chen, Vincent B et al. (2018) Caloric Restriction Engages Hepatic RNA Processing Mechanisms in Rhesus Monkeys. Cell Metab 27:677-688.e5
Ellis-Connell, Amy L; Balgeman, Alexis J; Zarbock, Katie R et al. (2018) ALT-803 Transiently Reduces Simian Immunodeficiency Virus Replication in the Absence of Antiretroviral Treatment. J Virol 92:
Park, Mi Ae; Jung, Ho Sun; Slukvin, Igor (2018) Genetic Engineering of Human Pluripotent Stem Cells Using PiggyBac Transposon System. Curr Protoc Stem Cell Biol 47:e63
Ellis, Amy; Balgeman, Alexis; Rodgers, Mark et al. (2017) Characterization of T Cells Specific for CFP-10 and ESAT-6 in Mycobacterium tuberculosis-Infected Mauritian Cynomolgus Macaques. Infect Immun 85:
Rodrigues, Michelle A (2017) Female Spider Monkeys (Ateles geoffroyi) Cope with Anthropogenic Disturbance Through Fission-Fusion Dynamics. Int J Primatol 38:838-855
Buechler, Connor R; Bailey, Adam L; Lauck, Michael et al. (2017) Genome Sequence of a Novel Kunsagivirus (Picornaviridae: Kunsagivirus) from a Wild Baboon (Papio cynocephalus). Genome Announc 5:
Wu, Hong; Whritenour, Jessica; Sanford, Jonathan C et al. (2017) Identification of MHC Haplotypes Associated with Drug-induced Hypersensitivity Reactions in Cynomolgus Monkeys. Toxicol Pathol 45:127-133
Shackman, A J; Fox, A S; Oler, J A et al. (2017) Heightened extended amygdala metabolism following threat characterizes the early phenotypic risk to develop anxiety-related psychopathology. Mol Psychiatry 22:724-732
Kalin, Ned H (2017) Mechanisms underlying the early risk to develop anxiety and depression: A translational approach. Eur Neuropsychopharmacol 27:543-553

Showing the most recent 10 out of 528 publications