The objective of the work is to design better techniques, particularly media, for in vitro fertilization and the culture of preimplantation embryos. The proposal is in two parts. The first part concerns the growth and differentiation of the mammalian blastocyst. Two animal models will be used, the mouse as a minimally expanding blastocyst, and the rabbit as a maximally expanding blastocyst. The response of the blastocysts to different media will be evaluated by measuring three major components of blastocyst development -- cell multiplication, the movement of fluid into the blastocyst and the synthesis of cell surface macromolecules. The initial phase will search for suitable available media that can provide the starting point for the addition of supplements such as amino acids and growth factors. Attempts will be made throughout to apply the principles of good experimental design to optimize the composition of media. The second part concerns finding suitable conditions for fertilizing primate oocytes in vitro. The purpose is to produce primate embryos for genetic manipulation, particularly to increase the numbers of genetically valuable animals for transfer, and by embryo bisection. The technique is also required for producing transgenic primates, which has importance in cancer research. Attempts will be made to increase the efficiency of in vitro fertilization in the rhesus monkey and the common marmoset.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01HD021988-05
Application #
3552545
Study Section
Special Emphasis Panel (SRC)
Project Start
1986-09-01
Project End
1991-08-31
Budget Start
1989-12-01
Budget End
1990-11-30
Support Year
5
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Erbach, Gregory T; Biggers, John D; Manning, Peter C et al. (2013) Localization of parathyroid hormone-related protein in the preimplantation mouse embryo is associated with events of blastocyst hatching. J Assist Reprod Genet 30:1009-15
Biggers, J D; McGinnis, L K (2001) Evidence that glucose is not always an inhibitor of mouse preimplantation development in vitro. Hum Reprod 16:153-163
Biggers, J D; McGinnis, L K; Raffin, M (2000) Amino acids and preimplantation development of the mouse in protein-free potassium simplex optimized medium. Biol Reprod 63:281-93
Summers, M C; McGinnis, L K; Lawitts, J A et al. (2000) IVF of mouse ova in a simplex optimized medium supplemented with amino acids. Hum Reprod 15:1791-801
Nowak, R A; Haimovici, F; Biggers, J D et al. (1999) Transforming growth factor-beta stimulates mouse blastocyst outgrowth through a mechanism involving parathyroid hormone-related protein. Biol Reprod 60:85-93
Biggers, J D; Summers, M C; McGinnis, L K (1997) Polyvinyl alcohol and amino acids as substitutes for bovine serum albumin in culture media for mouse preimplantation embryos. Hum Reprod Update 3:125-35
Younis, A I; Toner, M; Albertini, D F et al. (1996) Cryobiology of non-human primate oocytes. Hum Reprod 11:156-65
Erbach, G T; Bhatnagar, P; Baltz, J M et al. (1995) Zinc is a possible toxic contaminant of silicone oil in microdrop cultures of preimplantation mouse embryos. Hum Reprod 10:3248-54
Johnson, L D; Albertini, D F; McGinnis, L K et al. (1995) Chromatin organization, meiotic status and meiotic competence acquisition in mouse oocytes from cultured ovarian follicles. J Reprod Fertil 104:277-84
Feldman, B; Poueymirou, W; Papaioannou, V E et al. (1995) Requirement of FGF-4 for postimplantation mouse development. Science 267:246-9

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