Skeletal Biology Laboratory, School of Biological and Population Health Sciences, Oregon State University, Corvallis, OR, USA; Center for Healthy Aging Research, Oregon State University, Corvallis, OR, USA.
Bone. 2013 Nov;57(1):164-73. doi: 10.1016/j.bone.2013.08.002. Epub 2013 Aug 14.
The present studies investigated the cellular mechanisms for the detrimental effects of high dose whole body γ-irradiation on bone. In addition, radioadaptation and bone marrow transplantation were assessed as interventions to mitigate the skeletal complications of irradiation. Increased trabecular thickness and separation and reduced cancellous bone volume fraction, connectivity density, and trabecular number were detected in proximal tibia and lumbar vertebra 14days following γ-irradiation with 6Gy. To establish the cellular mechanism for the architectural changes, vertebrae were analyzed by histomorphometry 1, 3, and 14days following irradiation. Marrow cell density decreased within 1day (67% reduction, p<0.0001), reached a minimum value after 3days (86% reduction, p<0.0001), and partially rebounded by 14days (30% reduction, p=0.0025) following irradiation. In contrast, osteoblast-lined bone perimeter was increased by 290% (1day, p=0.04), 1230% (3days, p<0.0001), and 530% (14days, p=0.003), respectively. There was a strong association between radiation-induced marrow cell death and activation of bone lining cells to express the osteoblast phenotype (Pearson correlation -0.85, p<0.0001). An increase (p=0.004) in osteoclast-lined bone perimeter was also detected with irradiation. A priming dose of γ-radiation (0.5mGy), previously shown to reduce mortality, had minimal effect on the cellular responses to radiation and did not prevent detrimental changes in bone architecture. Bone marrow transplantation normalized marrow cell density, bone turnover, and most indices of bone architecture following irradiation. In summary, radiation-induced death of marrow cells is associated with 1) a transient increase in bone formation due, at least in part, to activation of bone lining cells, and 2) an increase in bone resorption due to increased osteoclast perimeter. Bone marrow transplantation is effective in mitigating the detrimental effects of acute exposure to high dose whole body γ-radiation on bone turnover.
本研究旨在探讨大剂量全身γ 射线照射对骨骼产生有害影响的细胞机制。此外,还评估了放射适应和骨髓移植作为减轻照射引起的骨骼并发症的干预措施。在给予 6Gy 全身γ 射线照射后 14 天,检测到胫骨近端和腰椎 1 处的小梁厚度增加、分离增加以及松质骨体积分数、连通密度和小梁数量减少。为了确定结构变化的细胞机制,在照射后 1、3 和 14 天对椎骨进行组织形态计量学分析。骨髓细胞密度在 1 天内下降(降低 67%,p<0.0001),在 3 天内达到最低值(降低 86%,p<0.0001),并在照射后 14 天部分反弹(降低 30%,p=0.0025)。相比之下,成骨细胞衬里骨周长增加了 290%(1 天,p=0.04)、1230%(3 天,p<0.0001)和 530%(14 天,p=0.003)。辐射诱导的骨髓细胞死亡与激活骨衬里细胞表达成骨细胞表型之间存在很强的相关性(Pearson 相关系数-0.85,p<0.0001)。还检测到照射后破骨细胞衬里骨周长增加(p=0.004)。先前已证明低剂量γ 辐射(0.5mGy)可降低死亡率,其对辐射细胞反应的影响很小,且不能防止骨结构的有害变化。骨髓移植使照射后骨髓细胞密度、骨转换和大多数骨结构指数正常化。总之,骨髓细胞的辐射诱导死亡与 1)由于至少部分原因骨衬里细胞的激活导致的短暂骨形成增加,和 2)由于破骨细胞周长增加导致的骨吸收增加有关。骨髓移植可有效减轻急性全身大剂量γ 射线照射对骨转换的有害影响。