Oocyte cryopreservation is of great importance to the advancement of assisted reproductive medicine, maintenance of animal resources, and livestock management. However, the commonly used methods today for oocyte cryopreservation by either slow-freezing or conventional vitrification have inherent drawbacks. For example, the slow-freezing (freezing: the transition of liquid water into ice crystal) approach is associated with inevitable cell injury due to ice formation and slow- freezing induced cell dehydration. The unusually high CPA (cryoprotectant) concentration (4 - 7 M) required by the conventional vitrification (vitrification: the transition of liquid water into an amorphous, glassy state rather than ice crystal) method can result in significant metabolic and osmotic injury in living cells even in a short exposure time of only a few minutes. Presumably, it is these inherent drawbacks that are responsible for the dismal outcome of oocyte cryopreservation to date. The goal of the proposed research outlined in this R01 proposal is to develop new strategies for cell cryopreservation by microencapsulating the cells in alginate microcapsule to vitrify at a low-CPA (low and non- toxic amount of cryoprotectants, = 1.5 M) concentration. The proposed low-CPA vitrification approach combines all the advantages of the commonly used slow-freezing and conventional vitrification techniques today while avoiding all their shortcomings. Oocytes of the naturally bred (outbred) Peromyscus will be used as the biological model in this project so that the results obtained from the proposed studies can be more transferable to achieve low-CPA vitrification of oocytes of other naturally bred mammals including humans. In addition, Peromyscus embryos will be used as the benchmark biological model in this project to test the new approach in view of the fact that embryo cryopreservation has been successful in general. It is believed that the proposed research and the novel low-CPA vitrification approach will have a significant impact on the field of oocyte cryopreservation for assisted reproductive medicine, maintenance of animal resources, and livestock management.

Public Health Relevance

Oocyte cryopreservation is of great importance to the advancement of assisted reproductive medicine. We propose to develop a novel technology to achieve much improved performance for oocyte cryopreservation. This research will have a significant impact on the preservation of future fertility of women who may lose gonadal function because of exposure to environmental/occupational hazards or aggressive medical treatments such as extirpative surgery, radiation, and chemotherapy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB012108-03
Application #
8209010
Study Section
Biomaterials and Biointerfaces Study Section (BMBI)
Program Officer
Hunziker, Rosemarie
Project Start
2011-03-01
Project End
2014-12-31
Budget Start
2012-01-01
Budget End
2012-12-31
Support Year
3
Fiscal Year
2012
Total Cost
$343,476
Indirect Cost
$115,344
Name
Ohio State University
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
Zhao, Shuting; Agarwal, Pranay; Rao, Wei et al. (2014) Coaxial electrospray of liquid core-hydrogel shell microcapsules for encapsulation and miniaturized 3D culture of pluripotent stem cells. Integr Biol (Camb) 6:874-84
Yi, Jingru; Liang, Xin M; Zhao, Gang et al. (2014) An improved model for nucleation-limited ice formation in living cells during freezing. PLoS One 9:e98132
Zhao, Gang; Takamatsu, Hiroshi; He, Xiaoming (2014) The effect of solution nonideality on modeling transmembrane water transport and diffusion-limited intracellular ice formation during cryopreservation. J Appl Phys 115:144701
Choi, Jung Kyu; Agarwal, Pranay; Huang, Haishui et al. (2014) The crucial role of mechanical heterogeneity in regulating follicle development and ovulation with engineered ovarian microtissue. Biomaterials 35:5122-8
Huang, Haishui; He, Xiaoming (2014) Interfacial tension based on-chip extraction of microparticles confined in microfluidic Stokes flows. Appl Phys Lett 105:143704
Choi, Jung Kyu; Agarwal, Pranay; He, Xiaoming (2013) In vitro culture of early secondary preantral follicles in hanging drop of ovarian cell-conditioned medium to obtain MII oocytes from outbred deer mice. Tissue Eng Part A 19:2626-37
Zhang, Wujie; Zhao, Shuting; Rao, Wei et al. (2013) A Novel Core-Shell Microcapsule for Encapsulation and 3D Culture of Embryonic Stem Cells. J Mater Chem B Mater Biol Med 2013:1002-1009
Agarwal, Pranay; Zhao, Shuting; Bielecki, Peter et al. (2013) One-step microfluidic generation of pre-hatching embryo-like core-shell microcapsules for miniaturized 3D culture of pluripotent stem cells. Lab Chip 13:4525-33
Choi, Jung Kyu; He, Xiaoming (2013) In vitro maturation of cumulus-oocyte complexes for efficient isolation of oocytes from outbred deer mice. PLoS One 8:e56158
He, Xiaoming (2011) Thermostability of biological systems: fundamentals, challenges, and quantification. Open Biomed Eng J 5:47-73

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