Light intensity and wavelength during embryo manipulation are important factors for maintaining viability of preimplantation embryos in vitro

Fertility and Sterility

Volumn 88, Issue 4 SUPPL., 2007, Pages 1150-1157

  Oh, Seo Jin ^a   Gong, Seung Pyo ^a   Lee, Seung Tae ^a   Lee, Eun Ju ^a   Lim, Jeong Mook ^a  

^a Seoul National University   (South Korea)

Author keywords

apoptosis; Hamster embryo; Hsp70; lighting; preimplantation development; reactive oxygen species (ROS)

Indexed keywords

HEAT SHOCK PROTEIN 70; REACTIVE OXYGEN METABOLITE;

ANIMAL CELL; APOPTOSIS; ARTICLE; BLASTOCYST; BLASTOMERE; BLUE LIGHT; CELL MANIPULATION; CELL VIABILITY; CONTROLLED STUDY; EMBRYO; EMBRYO CULTURE; EMBRYO DEVELOPMENT; FEMALE; HAMSTER; LIGHT INTENSITY; MALE; MORULA; NONHUMAN; NUCLEOTIDE SEQUENCE; PREIMPLANTATION EMBRYO; PRIORITY JOURNAL; PROTEIN EXPRESSION; RANDOMIZATION; RED LIGHT; SPECTRAL SENSITIVITY;

ANIMALS; BASE SEQUENCE; BLASTOCYST; CELL SURVIVAL; CRICETINAE; EMBRYO TRANSFER; EMBRYONIC DEVELOPMENT; FEMALE; LIGHT; MALE; MOLECULAR SEQUENCE DATA; PREGNANCY; PROSPECTIVE STUDIES; RANDOM ALLOCATION;

EID: 34848919748     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2007.01.036     Document Type: Article

References (32)

1. Rinehart J.S., Bavister B.D., and Gerrity M. Quality control in the in vitro fertilization laboratory: comparison of bioassay systems for water quality. J In Vitro Fert Embryo Transf 5 (1988) 335-342
2. Isfort R.J., Kerckaert G.A., Cody D.B., Carter J., Driscoll K.E., and LeBoeuf R.A. Isolation and biological characterization of morphological transformation-sensitive Syrian hamster embryo cells. Carcinogenesis 17 (1996) 997-1005
3. Riley J.K., and Moley K.H. Glucose utilization and the PI3-K pathway: mechanisms for cell survival in preimplantation embryos. Reproduction 131 (2006) 823-835
4. Warner S.M., Conlon F.V., and Kane M.T. Inositol transport in preimplantation rabbit embryos: effects of embryo stage, sodium, osmolality and metabolic inhibitors. Reproduction 129 (2005) 128
5. Van Blerkom J. Mitochondria in human oogenesis and preimplantation embryogenesis: engines of metabolism, ionic regulation and developmental competence. Reproduction 128 (2004) 269-280
6. Houghton F.D., and Leese H.J. Metabolism and developmental competence of the preimplantation embryo. Eur J Obstet Gynecol Reprod Biol (2004) 115 (Suppl 1):S92-6
7. Kolle S., Stojkovic M., Reese S., Reichenbach H.D., Wolf E., and Sinowatz F. Effects of growth hormone on the ultrastructure of bovine preimplantation embryos. Cell Tissue Res 317 (2004) 101-108
8. Lee ST, Oh SJ, Lee EJ, Ho J Han, Lim JM. Adenosine triphosphate synthesis, mitochondrial number and activity, and pyruvate uptake in oocytes following gonadotropin injections. Fertil Steril 2006;86:1164-9.
9. Lee S.T., Han H.J., Oh S.J., Lee E.J., Han J.Y., and Lim J.M. Influence of ovarian hyperstimulation and ovulation induction on cytoskeletal dynamics and developmental competence of oocytes. Mol Reprod Dev 73 (2006) 1022-1033
10. Brackett B.G. Recent progress in investigations of fertilization in vitro. In: Blandaau R.J. (Ed). The biology of the blastocyst (1971), University of Chicago, Chicago 329-348
11. Chang M.O., and Sharkey N.A. Recent advances in fertilization of mammalian eggs in vitro. In: Afzelius B.J. (Ed). The functional anatomy of the spermatozoa (1977), Pergamon, Oxford/New York 97-103
12. Gwatkin R.B.L. Fertilization mechanisms in man and mammals (1977), Plenum, New York
13. Yanagimachi R. Specificity of sperm-egg interation. In: Edidin M., and Johnsonn M.H. (Eds). Immunobiology of gametes (1977), Cambridge University Press, Cambridge 9:255-95
14. Schumacher A., and Fisher B. Influence of visible light and room temperature on cell proliferation in preimplantation rabbit embryos. J Reprod Fertil 84 (1988) 197-204
15. Ludwig T.E., Squirrell J.M., Palmenberge A.C., and Bavister B.D. Relationship between development, metabolism, and mitochondrial organization in two-cell hamster embryos in the presence of low levels of phosphate. Biol Reprod 65 (2001) 1648-1654
16. Lane M., Boatman D.E., Albert R.M., and Bavister B.D. Intracellular divalent cation homeostasis and developmental competence in the hamster preimplantation embryo. Mol Reprod Dev 50 (1998) 443-450
17. Yang H.W., Hwang K.J., Kwon H.C., Kim H.S., Choi K.W., and Oh K.S. Detection of reactive oxygen species (ROS) and apoptosis in human fragmented embryos. Hum Reprod 13 (1998) 998-1002
18. Hashimoto S., Minomi N., Takakura R., Yamada M., Imai H., and Kashima N. Low oxygen tension during in vitro maturation is beneficial for supporting the subsequent development of bovine cumulus-oocyte complexes. Mol Reprod Dev 57 (2000) 112-119
19. Gavrieli Y., Sherman Y., and Ben-Sasson S.A. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J Cell Biol 119 (1992) 493-501
20. Brison D.R., and Schultz R.M. Apoptosis during mouse blastocyst formation: evidence for a role for survival factors including transforming growth factor α. Biol Reprod 56 (1997) 1088-1096
21. Byrne A.T., Southgate J., Brison D.R., and Leese H.J. Analysis of apoptosis in the preimplantation bovine embryo using TUNEL. J Reprod Fertil 117 (1999) 97-105
22. Knijn H.M., Gørret J.O., Vos P.I.A.M., Hendrikesn P.J.M., van der Weiiden B.C., Maddox-Hyttel P., et al. Consequences of in vivo development and subsequent culture on apoptosis, cell number, and blastocyst formation in bovine embryos. Biol Reprod 69 (2003) 1371-1378
23. Benjamin I.J., and McMillan D.R. Stress (heat shock) proteins, molecular chaperones in cardiovascular biology and disease. Circ Res 83 (1998) 117-132
24. Feder M.E., and Hofmann G.E. Heat shock proteins, molecular chaperones, and the stress response: evolutionary and ecological physiology. Annu Rev Physiol 61 (1999) 243-282
25. Jolly C., and Morimoto R.I. Role of heat shock response and molecular chaperones in oncogenesis and cell death. J Natl Cancer Inst 92 (2000) 1564-1572
26. Lindquist S. The heat shock response. Annu Rev Biochem 55 (1986) 1151-1191
27. Smith D.F., Whitesell L., and Katsanis E. Molecular chaperones: biology and prospects for pharmacological intervention. Pharmacol Rev 50 (1998) 493-513
28. Beere H.M., and Green D.R. Stress-management heat shock protein-70 and the regulation of apoptosis. Trends Cell Biol 11 (2001) 6-10
29. Agashe V.R., and Hartl F.-U. Role of molecular chaperones in cytoplasmic protein folding. Semin Cell Dev Biol 11 (2000) 15-25
30. Gething M.J., and Sambrook J. Protein folding in the cell. Nature 355 (1992) 33-45
31. Lesser M.P., Kruse V.A., and Barry T.M. Exposure to ultraviolet radiation causes apoptosis in developing sea urchin embryos. J Exp Biol (2003) 206 Pt 22:4097-103
32. Felip A., Piferrer F., Carrillo M., and Zanuy S. The relationship between the effects of UV light and thermal shock on gametes and the viability of early developmental stages in a marine teleost fish, the sea bass (Dicentrarchus labrax L.). Heredity (1999) 83 Pt 4:387-97