Department of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Department of Surgery, Indiana University School of Medicine, Indianapolis, IN.
Health Phys. 2020 Nov;119(5):633-646. doi: 10.1097/HP.0000000000001344.
Development of medical countermeasures against radiation relies on robust animal models for efficacy testing. Mouse models have advantages over larger species due to economics, ease of conducting aging studies, existence of historical databases, and research tools allowing for sophisticated mechanistic studies. However, the radiation dose-response relationship of inbred strains is inherently steep and sensitive to experimental variables, and inbred models have been criticized for lacking genetic diversity. Jackson Diversity Outbred (JDO) mice are the most genetically diverse strain available, developed by the Collaborative Cross Consortium using eight founder strains, and may represent a more accurate model of humans than inbred strains. Herein, models of the Hematopoietic-Acute Radiation Syndrome and the Delayed Effects of Acute Radiation Exposure were developed in JDO mice and compared to inbred C57BL/6. The dose response relationship curve in JDO mice mirrored the more shallow curves of primates and humans, characteristic of genetic diversity. JDO mice were more radioresistant than C57BL/6 and differed in sensitivity to antibiotic countermeasures. The model was validated with pegylated-G-CSF, which provided significantly enhanced 30-d survival and accelerated blood recovery. Long-term JDO survivors exhibited increased recovery of blood cells and functional bone marrow hematopoietic progenitors compared to C57BL/6. While JDO hematopoietic stem cells declined more in number, they maintained a greater degree of quiescence compared to C57BL/6, which is essential for maintaining function. These JDO radiation models offer many of the advantages of small animals with the genetic diversity of large animals, providing an attractive alternative to currently available radiation animal models.
开发针对辐射的医学对策依赖于用于功效测试的强大动物模型。由于经济、易于进行老化研究、存在历史数据库以及允许进行复杂机制研究的研究工具,小鼠模型相对于较大的物种具有优势。然而,近交系的辐射剂量-反应关系本质上是陡峭的,并且对实验变量敏感,并且近交模型因缺乏遗传多样性而受到批评。Jackson Diversity Outbred (JDO) 小鼠是可用的遗传多样性最高的品系,由 Collaborative Cross 联盟使用八个创始品系开发,与近交系 C57BL/6 相比,可能代表更准确的人类模型。在此,开发了造血-急性辐射综合征和急性辐射暴露延迟效应的 JDO 小鼠模型,并与近交系 C57BL/6 进行了比较。JDO 小鼠的剂量反应关系曲线反映了灵长类动物和人类更浅的曲线,这是遗传多样性的特征。JDO 小鼠比 C57BL/6 更具辐射抗性,并且对抗生素对策的敏感性不同。该模型用聚乙二醇化-G-CSF 进行了验证,聚乙二醇化-G-CSF 提供了显着提高的 30 天存活率并加速了血液恢复。与 C57BL/6 相比,长期 JDO 幸存者表现出血液细胞和功能性骨髓造血祖细胞的恢复增加。虽然 JDO 造血干细胞的数量减少更多,但它们与 C57BL/6 相比保持更大程度的静止,这对于维持功能至关重要。这些 JDO 辐射模型具有许多小动物的优势,同时具有大型动物的遗传多样性,为目前可用的辐射动物模型提供了有吸引力的替代方案。