Abstract
Radiation damage due to total body irradiation (TBI) or targeted abdominal radiation can deplete ovarian follicles and accelerate reproductive aging. We characterized a mouse model of low-dose TBI to investigate how radiation affects the follicular and stromal compartments of the ovary. A single TBI dose of either 0.1 Gy or 1 Gy (Cesium-137 γ) was delivered to reproductively adult CD1 female mice, and sham-treated mice served as controls. Mice were euthanized either 2 weeks or 5 weeks post exposure, and ovarian tissue was harvested. To assess the ovarian reserve, we classified and counted the number of morphologically normal follicles in ovarian histologic sections for all experimental cohorts using an objective method based on immunohistochemistry for an oocyte-specific protein (MSY2). 0.1 Gy did not affect that total number of ovarian follicles, whereas 1 Gy resulted in a dramatic loss. At two weeks, there was a significant reduction in all preantral follicles, but early antral and antral follicles were still present. By five weeks, there was complete depletion of all follicle classes. We examined stromal quality using histologic stains to visualize ovarian architecture and fibrosis and by immunohistochemistry and quantitative microscopy to assess cell proliferation, cell death and vasculature. There were no differences in the ovarian stroma across cohorts with respect to these markers, indicating that this compartment is more radio-resistant relative to the germ cells. These findings have implications for reproductive health and the field of fertility preservation because the radiation doses we examined mimic scatter doses experienced in typical therapeutic regimens.
Original language | English (US) |
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Pages (from-to) | 553-562 |
Number of pages | 10 |
Journal | Reproduction |
Volume | 155 |
Issue number | 6 |
DOIs | |
State | Published - 2018 |
Funding
The authors would like to thank Jing Huang (KUMC Histology Core) and Megan Larmore (University of Washington Histology and Imaging Core) for their technical assistance in ovarian tissue sectioning and quantitative microscopy analysis, respectively. This work was supported by the Center for Reproductive Health After Disease (P50 HD076188; pilot project to F E D) from the National Centers for Translational Research in Reproduction and Infertility (NCTRI). The KUMC Histology Core was supported by the P30 HD002528 (Kansas IDDRC).
ASJC Scopus subject areas
- Endocrinology
- Obstetrics and Gynecology
- Cell Biology
- Reproductive Medicine
- Embryology