Department of Biomedical Engineering, Stony Brook University, Stony Brook, NY 11794-2580, USA.
J Bone Miner Res. 2012 Apr;27(4):749-59. doi: 10.1002/jbmr.1505.
Stem cell depletion and compromised bone marrow resulting from radiation exposure fosters long-term deterioration of numerous physiologic systems, with the degradation of the skeletal system ultimately increasing the risk of fractures. To study the interrelationship of damaged bone marrow cell populations with trabecular microarchitecture, 8- and 16-week-old C57BL/6 male mice were sublethally irradiated with 5 Gy of (137)Cs γ-rays, and adult stem cells residing in the bone marrow, as well as bone quantity and quality, were evaluated in the proximal tibia after 2 days, 10 days, and 8 weeks compared with age-matched controls. Total extracted bone marrow cells in the irradiated 8-week, young adult mice, including the hematopoietic cell niches, collapsed by 65% ± 11% after 2 days, remaining at those levels through 10 days, only recovering to age-matched control levels by 8 weeks. As early as 10 days, double-labeled surface was undetectable in the irradiated group, paralleled by a 41% ± 12% and 33% ± 4% decline in bone volume fraction (BV/TV) and trabecular number (Tb.N), respectively, and a 50% ± 10% increase in trabecular separation (Tb.Sp) compared with the age-matched controls, a compromised structure that persisted to 8 weeks postirradiation. Although the overall collapse of the bone marrow population and devastation of bone quality was similar between the "young adult" and "mature" mice, the impact of irradiation--and the speed of recovery--on specific hematopoietic subpopulations was dependent on age, with the older animals slower to restore key progenitor populations. These data indicate that, independent of animal age, complications arising from irradiation extend beyond the collapse of the stem cell population and extend toward damage to key organ systems. It is reasonable to presume that accelerating the recovery of these stem cell pools will enable the prompt repair of the skeletal system and ultimately reduce the susceptibility to fractures.
辐射导致的干细胞耗竭和骨髓损伤会促进众多生理系统的长期恶化,骨骼系统的退化最终会增加骨折的风险。为了研究受损骨髓细胞群体与骨小梁微观结构的相互关系,将 8 周和 16 周龄的 C57BL/6 雄性小鼠用 5Gy(137)Csγ射线亚致死照射,并在 2 天、10 天和 8 周后与年龄匹配的对照组比较,评估其骨髓内的成体干细胞以及骨量和骨质量。照射后 8 周的年轻成年小鼠,包括造血细胞龛位,总提取骨髓细胞在 2 天内减少了 65%±11%,在 10 天内保持在这些水平,直到 8 周才恢复到与年龄匹配的对照组水平。早在 10 天,双标记表面在照射组中就无法检测到,骨体积分数(BV/TV)和小梁数(Tb.N)分别下降了 41%±12%和 33%±4%,小梁间隔(Tb.Sp)增加了 50%±10%,与年龄匹配的对照组相比,结构受损一直持续到照射后 8 周。尽管“年轻成年”和“成熟”小鼠的骨髓细胞群总体崩溃和骨质量破坏相似,但照射的影响及其对特定造血亚群的恢复速度取决于年龄,老年动物恢复关键祖细胞群体的速度较慢。这些数据表明,无论动物年龄如何,辐射引起的并发症不仅限于干细胞群体的崩溃,还会扩展到关键器官系统的损伤。可以合理地假设,加速这些干细胞库的恢复将使骨骼系统能够迅速得到修复,并最终降低骨折的易感性。