The objectives of this application are to devise protocols for the production of developmentally competent in vitro matured primate oocytes and to develop methods for cryopreservation of NHP oocytes. This project integrates the expertise and resources of investigators at three Regional Primate Research Centers (RPRCs) to address these complimentary objectives. At present, the success rate for IVM of oocytes is markedly reduced compared to in vivo matured oocytes, especially for IVM of oocytes from non-stimulated ovaries. Initial experiments will utilize oocytes from seven-day follicle stimulated hormone (FSH)-primed females, but as success improves, oocytes from four-day FSH-primed and non-stimulated ovaries will be used in experiments. Improvement of IVM methods will include the development of culture conditions that maintain the cumulus-oocyte connections and reversibly inhibit nuclear maturation. Once these methods are devised, a two-step procedure for IVM can be developed. The first step will delay nuclear maturation and allow the study of methods to improve cytoplasmic maturation. The second step will allow and promote nuclear maturation. In parallel experiments, the investigators will continue with efforts to improve methods for cryopreservation of mature and immature oocytes. A key part of the approach will be to determine whether organic osmolytes and/or other media supplements alter the sensitivity of oocytes to chilling injury or osmotic shock. Subsequent experiments will derive equilibrium and non-equilibrium (vitrification) methods for cryopreservation. Both IVM and cryopreservation can cause damage to oocytes, which results in decreased developmental competence of the embryos. Until alterations in the procedures for IVM and cryopreservation become more successful, another technique may provide an interim solution for improving the developmental competence of these oocytes. Transfer of cytoplasm from in vivo matured, developmentally competent oocytes to IVM or frozen/thawed oocytes may overcome their reduced developmental competence. An effective system of primate oocyte cryopreservation and IVM would provide a means to make large numbers of oocytes available for studies on early development and would assist primate breeding and conservation efforts.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Research Project (R01)
Project #
5R01RR013439-08
Application #
6916314
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Program Officer
Rall, William F
Project Start
1998-08-01
Project End
2007-07-31
Budget Start
2005-08-01
Budget End
2006-07-31
Support Year
8
Fiscal Year
2005
Total Cost
$601,734
Indirect Cost
Name
University of California Davis
Department
Veterinary Sciences
Type
Other Domestic Higher Education
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Puttabyatappa, Muraly; Brogan, Rebecca S; Vandevoort, Catherine A et al. (2013) EGF-like ligands mediate progesterone's anti-apoptotic action on macaque granulosa cells. Biol Reprod 88:18
Mtango, Namdori R; Sutovsky, Miriam; Vandevoort, Catherine A et al. (2012) Essential role of ubiquitin C-terminal hydrolases UCHL1 and UCHL3 in mammalian oocyte maturation. J Cell Physiol 227:2022-9
Mtango, Namdori R; VandeVoort, Catherine A; Latham, Keith E (2011) Ontological aspects of pluripotency and stemness gene expression pattern in the rhesus monkey. Gene Expr Patterns 11:285-98
Tollner, Theodore L; Dong, Qiaoxiang; VandeVoort, Catherine A (2011) Frozen-thawed rhesus sperm retain normal morphology and highly progressive motility but exhibit sharply reduced efficiency in penetrating cervical mucus and hyaluronic acid gel. Cryobiology 62:15-21
Dong, Qiao-Xiang; Rodenburg, Sarah E; Hill, Dana et al. (2011) The role of low-density lipoprotein (LDL) and high-density lipoprotein (HDL) in comparison with whole egg yolk for sperm cryopreservation in rhesus monkeys. Asian J Androl 13:459-64
Duffy, Diane M; VandeVoort, Catherine A (2011) Maturation and fertilization of nonhuman primate oocytes are compromised by oral administration of a cyclooxygenase-2 inhibitor. Fertil Steril 95:1256-60
Brogan, Rebecca S; MacGibeny, Margaret; Mix, Scott et al. (2011) Dynamics of intra-follicular glucose during luteinization of macaque ovarian follicles. Mol Cell Endocrinol 332:189-95
Vandevoort, Catherine A; Mtango, Namdori R; Latham, Keith E et al. (2011) Primate preimplantation embryo is a target for relaxin during early pregnancy. Fertil Steril 96:203-7
Dong, Qiaoxiang; Tollner, Theodore L; Rodenburg, Sarah E et al. (2010) Antioxidants, Oxyrase, and mitochondrial uncoupler 2,4-dinitrophenol improved postthaw survival of rhesus monkey sperm from ejaculates with low cryosurvival. Fertil Steril 94:2359-61
Duffy, Diane M; McGinnis, Lynda K; Vandevoort, Catherine A et al. (2010) Mammalian oocytes are targets for prostaglandin E2 (PGE2) action. Reprod Biol Endocrinol 8:131

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