Unlaid Eggs: Ovarian Damage after Low-Dose Radiation.
Elisabeth ReiserMaria Victoria BazzanoMaria Emilia SolanoJohannes HaybaeckChristoph SchatzJulian MangesiusUte GanswindtBettina TothPublished in: Cells (2022)
The total body irradiation of lymphomas and co-irradiation in the treatment of adjacent solid tumors can lead to a reduced ovarian function, premature ovarian insufficiency, and menopause. A small number of studies has assessed the radiation-induced damage of primordial follicles in animal models and humans. Studies are emerging that evaluate radiation-induced damage to the surrounding ovarian tissue including stromal and immune cells. We reviewed basic laboratory work to assess the current state of knowledge and to establish an experimental setting for further studies in animals and humans. The experimental approaches were mostly performed using mouse models. Most studies relied on single doses as high as 1 Gy, which is considered to cause severe damage to the ovary. Changes in the ovarian reserve were related to the primordial follicle count, providing reproducible evidence that radiation with 1 Gy leads to a significant depletion. Radiation with 0.1 Gy mostly did not show an effect on the primordial follicles. Fewer data exist on the effects of radiation on the ovarian microenvironment including theca-interstitial, immune, endothelial, and smooth muscle cells. We concluded that a mouse model would provide the most reliable model to study the effects of low-dose radiation. Furthermore, both immunohistochemistry and fluorescence-activated cell sorting (FACS) analyses were valuable to analyze not only the germ cells but also the ovarian microenvironment.
Keyphrases
- radiation induced
- low dose
- radiation therapy
- mouse model
- oxidative stress
- stem cells
- case control
- healthcare
- induced apoptosis
- mesenchymal stem cells
- single cell
- electronic health record
- germ cell
- cell death
- postmenopausal women
- machine learning
- single molecule
- artificial intelligence
- big data
- cell therapy
- cell cycle arrest
- endoplasmic reticulum stress
- drug induced