An Assay Using Embryo Aggregation Chimeras for the Detection of Nonlethal Changes in X-Irradiated Mouse Preimplantation Embryos

• Published in: Radiation research 1988-02, Vol.113 (2), p.289-299
• Main Authors: Obasaju, Michael Femi, Wiley, Lynn M., Oudiz, Deborah J., Miller, Lisa, Samuels, Steven J., Chang, R. Jeffrey, Overstreet, James W.
• Format: Article
• Language: English
• Subjects: Aggregation; Animals; Blastocyst - radiation effects; Blastomeres; Cell growth; Chimera; Chimeras; Cultured cells; Dose response relationship; Embryo, Mammalian; Embryonic cells; Embryos; Female; Fluorescein-5-isothiocyanate; Fluoresceins; Irradiation; Mice; Pregnancy; Radiation dosage; Space life sciences; Thiocyanates
• ISSN: 0033-7587; 1938-5404
• DOI: 10.2307/3577204

We have developed a short-term in vitro assay for the detection of sublethal effects produced by very low levels of ionizing radiation. The assay utilizes mouse embryo aggregation chimeras consisting of one irradiated embryo paired with an unirradiated embryo whose blastomeres have been labeled with fluorescein isothiocyanate (FITC). X irradiation (from 0.05 to 2 Gy) and chimera construction were performed with four-cell stage embryos, and the chimeras were cultured for 40 h to the morula stage. The morulae were partially dissociated with calcium-free culture medium and viewed under phase contrast and epifluorescence microscopy to obtain total embryo cell number and the cellular contribution of irradiated (unlabeled) and control (FITC labeled) embryos per chimera. In chimeras where neither embryo was irradiated, the ratio of the unlabeled blastomeres to the total number of blastomeres per chimera embryo was 0.50 (17.8 ± 5.6 cells per unlabeled embryo and 17.4 ± 5.5 cells per FITC-labeled partner embryo). However, in chimeras formed after the unlabeled embryos were irradiated with as little as 0.05 Gy, the ratio of unlabeled blastomeres to the total number of blastomeres per chimera embryo was 0.43 (P < 0.01). The apparent decreases in cell proliferation were not observed in irradiated embryos that were merely cocultured with control embryos, regardless of whether the embryos were zona enclosed or zona free. We conclude that very low levels of radiation induce sublethal changes in cleaving embryos that are expressed as a proliferative disadvantage within two cell cycles when irradiated embryos are in direct cell-to-cell contact with unirradiated embryos.