Anatomy and Embryology

, Volume 183, Issue 6, pp 559–571 | Cite as

Effects of visible light and room temperature on the ultrastructure of preimplantation rabbit embryos: a time course study

  • Christa Hegele-Hartung
  • Armin Schumacher
  • Bernd Fischer
Original Articles

Summary

In a time course study (4–20 h) rabbit early cleavage stages (day 1 p.c.) and compacted morulae (day 3 p.c.) were exposed to visible light or room temperature (23° C), respectively. An 8 h light exposure of day 1 embryos caused alterations in nuclear morphology (lobulated nuclei, loss of nucleolar diffentiation), an increased electron density of the cytoplasm, and cellular fragmentation leading to a considerable degeneration of blastomeres (central clustering of organelles, loss of cell surface differentiation) after a 20 h exposure. Room temperature exposure (compacted Day 3 morulae) led to decompaction and a cleavage delay after 8 h. After 10 h, arrested metaphases occurred in all examined morulae. Even after 20 h at 23° C, day 3 embryos were at the decompacted morula stage, and showed metaphase-arrested blastomeres. The general morphology of the blastomeres was unaffected at this temperature, except for vacuolated serand cis-side vesicles of the Golgi complex at 8, 12 and 20 h, respectively.

Key words

Visible light Room temperature Pre-implantation embryos Rabbit TEM 

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References

  1. Anderson E, Condon W, Sharp D (1971) A study of oogenesis and early embryogenesis in the rabbit, Oryctolagus cuniculus, with special reference to the structural changes of mitochondria. J Morphol 130:67–92Google Scholar
  2. Bavister BD (1987) Studies on the developmental blocks in cultured hamster embryos. In: Bavister BD (ed) The mammalian preimplantation embryo. Regulation of growth and differentiation in vitro. Plenum Press, New York, pp 219–249Google Scholar
  3. Bavister BD (1988) Role of oviductal secretions in embryonic growth in vivo and in vitro. Theriogenology 29:143–154Google Scholar
  4. Chang MC (1948) The effects of low temperature on fertilized rabbit ova in vitro, and the normal development of ova kept at low temperature for several days. J Gen Physiol 31:385–409Google Scholar
  5. Clarke PGH (1990) Developmental cell death: morphological diversity and multiple mechanisms. Anat Embryol 181:195–213PubMedGoogle Scholar
  6. Danielsen EM, Hansen GH, Cowell GM (1989) Biosynthesis of intestinal microvillar proteins. Low temperature arrests both processing and intracellular transport. Eur J Cell Biol 49:123–127Google Scholar
  7. Fischer B (1987) Development retardation in cultured preimplantation rabbit embryos. J Reprod Fertil 79:115–123Google Scholar
  8. Fischer B (1988) Embryonalentwicklung in vitro und in vivo. Charakterisierung entwicklungsspezifischer Strukturen und Lebensäußerungen von Präimplantationsembryonen in vitro und in vivo. Copythek, Enke, StuttgartGoogle Scholar
  9. Fischer B (1989) Effects of asynchrony on rabbit blastocyst development. J Reprod Fertil 86:479–491PubMedGoogle Scholar
  10. Fischer B, Meuser-Odenkirchen G (1988) A 2-year follow-up of effects of biotechniques on reproduction in the domestic rabbit, Oryctolagus cuniculus. Lab Anim 22:5–15Google Scholar
  11. Fischer B, Schumacher A, Hegele-Hartung C, Beier HM (1988) Potential risk of light and room temperature exposure to preimplantation embryos. Fertil Steril 50:938–944Google Scholar
  12. Hegele-Hartung C, Fischer B, Beier HM (1988a) Development of preimplantation rabbit embryos after in vitro culture and embryo transfer: an electron microscopic study. Anat Rec 220:31–42Google Scholar
  13. Hegele-Hartung C, Schumacher A, Fischer B (1988b) Ultrastructure of preimplantation rabbit embryos exposed to visible light and room temperature. Anat Embryol 178:229–241Google Scholar
  14. Hegele-Hartung C, Piegsa K, Fischer B (1989) Effect of osmolarity of the fixative on the ultrastructure of preimplantation rabbit embryos. Acta Anat 136:79–88Google Scholar
  15. Hesseldahl H (1971) Ultrastructure of early cleavage stages and preimplantation in the rabbit. Z Anat Entwicklungsgesch 135:139–135Google Scholar
  16. Inoué S (1981) Cell division and the mitotic spindle. J Cell Biol 91:131s-147sGoogle Scholar
  17. Kane MT (1987a) Culture media and culture of early embryos. Theriogenology 27:49–57Google Scholar
  18. Kane MT (1987b) In vitro growth of preimplantation rabbit embryos. In: Bavister BD (ed) The mammalian preimplantation embryo. Plenum Press, New York, pp 193–217Google Scholar
  19. Kane MT, Foote RH (1970) Culture of two-and four-cell rabbit embryos to the expanding blastocyst stage in synthetic media. Proc Soc Exp Biol Med 133:921–925Google Scholar
  20. Kane MT, Foote RH (1971) Factors affecting blastocyst expansion of rabbit zygotes and young embryos in defined media. Biol Reprod 4:41–47Google Scholar
  21. Karp LE, Smith WD (1975) Experimental production of aneuploidy in mouse oocytes. Gynecol Invest 6:337–341Google Scholar
  22. Kerr JFR, Bishop CJ, Searly J (1984) Apoptosis. Recent Adv Histopathol 12:1–15Google Scholar
  23. King WA, Niar A, Chartrain I, Betteridge KJ, Guay P (1988) Nucleolus organizer regions and nucleoli in preattachment bovine embryos. I Reprod Fertil 82:87–95Google Scholar
  24. Lambert AM, Bajer AS (1977) Microtubule distribution and reversible arrest of chromosome movements induced by low temperature. Cytobiologie 15:1–23Google Scholar
  25. Magistrini M, Szöllösi D (1980) Effects of cold and of isopropyl-Nphenylcarbonate on the second meiotic spindle of mouse oocytes. Eur J Cell Biol 22:699–707Google Scholar
  26. Manes C (1973) The participation of the embryonic genome during early cleavage in the rabbit. Dev Biol 32:453–459Google Scholar
  27. Manes C (1977) Nucleic acid synthesis in preimplantation rabbit embryos. III. A “dark period” immediately following fertilization, and the early predominance low molecular weight RNA synthesis. J Exp Zool 201:247–258Google Scholar
  28. Overström EW (1987) In vitro assessment of blastocyst differentiation. In: Bavister BD (ed) The mammalian preimplantation embryo. Regulation of growth and differentiation in vitro. Plenum Press, New York, pp 95–116Google Scholar
  29. Pickering SJ, Johnson MH (1987) The influence of cooling on the organization of the meiotic spindle of the mouse oocyte. Hum Reprod 2:207–216Google Scholar
  30. Saraste J, Kuismanen E (1984) Preand post-Golgi vacuoles operate in the transport of Semliki forest virus membrane glycoproteins to the cell surface. Cell 38:535–549Google Scholar
  31. Saraste J, Palade GE, Farguhar MG (1986) Temperature-sensitive steps in the transport of secretory proteins through the Golgi complex in exocrine pancreatic cells. Proc Natl Acad Sci USA 83:6425–6429Google Scholar
  32. Sathananthan AH, Trounson A, Freeman L, Brady T (1988) The effects of cooling human oocytes. Hum Reprod 3:968–977Google Scholar
  33. Schumacher A, Fischer B (1988) The influence of visible light and room temperature on cell proliferation in preimplantation rabbit embryos. J Reprod Fertil 84:197–204Google Scholar
  34. Schumacher A, Hegele-Hartung C, Mootz U, Beier HM, Fischer B (1989) Developmental capacity of preimplantation rabbit embryos injured by exposure to visible light or room temperature. J Reprod Fertil Abstract Series No. 3:19 (abstr. 28)Google Scholar
  35. Spielmann H (1987) Analysis of embryo toxic effects in preimplantation embryos. In: Bavister BD (ed) The mammalian preimplantation embryo. Regulation of growth and differentiation in vitro. Plenum Press, New York, pp 309–331Google Scholar
  36. Sundström P, Nilsson O, Liedholm P (1981) Cleavage rate and morphology of early human embryos obtained after artificial fertilization and culture. Acta Obstet Gynecol Scand 60:109–120Google Scholar
  37. Trounson A, Sathananthan AH (1984) The application of electron microscopy in the evaluation of two-to four-cell human embryos cultured in vitro for embryo transfer. J In Vitro Fert Embryo Transfer 1:153–165Google Scholar
  38. Van Blerkom J, Manes C, Daniel JC Jr (1973) Development of preimplantation rabbit embryos in vivo and in vitro. Dev Biol 35:262–282Google Scholar
  39. Wyllie AH (1987) Apoptosis. Cell death under homeostatic control. Arch Toxicol [Suppl] 11:3–10Google Scholar

Copyright information

© Springer-Verlag 1991

Authors and Affiliations

  • Christa Hegele-Hartung
    • 1
  • Armin Schumacher
    • 1
  • Bernd Fischer
    • 1
  1. 1.Department of Anatomy and Reproductive BiologyMedical Faculty of the RWTH AachenAachenFederal Republic of Germany

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