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Acute Exposure to High Dose γ-Radiation Results in Transient Activation of Bone Lining Cells

机译:急性暴露于高剂量γ射线会导致骨衬细胞的瞬时活化

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摘要

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 fractional cancellous bone volume, connectivity density, and trabecular number were detected in proximal tibia and lumbar vertebra 14 days following γ-irradiation with 6 Gy. To establish the cellular mechanism for the architectural changes, vertebrae were analyzed by histomorphometry 1, 3, and 14 days following irradiation. Marrow cell density decreased within 1 day (67% reduction, p<0.0001), reached a minimum value after 3 days (86% reduction, p<0.0001), and partially rebounded by 14 days (30% reduction, p=0.0025) following irradiation. In contrast, osteoblast-lined bone perimeter was increased by 290% (1 day, p=0.04), 1230% (3 days, p<0.0001), and 530% (14 days, 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 (0.5 mGy), 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.
机译:本研究研究了高剂量全身γ射线对骨骼有害作用的细胞机制。另外,评估了放射适应和骨髓移植作为减轻辐射的骨骼并发症的干预措施。接受6 Gyγ射线照射14天后,在胫骨近端和腰椎中发现了小梁厚度增加和分离,并减少了松质骨分数,连通性密度和小梁数量。为了建立改变结构的细胞机制,在照射后第1、3和14天通过组织形态测定法分析椎骨。骨髓细胞密度在1天内下降(下降67%,p <0.0001),在3天后达到最小值(下降86%,p <0.0001),并在14天后部分反弹(下降30%,p = 0.0025)辐射。相反,成骨细胞内衬的骨周长分别增加了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骨衬细胞激活以表达成骨细胞表型之间存在密切的关联(Pearson相关系数-0.85,p <0.0001)。辐照也检测到破骨细胞衬里的骨周长增加(p = 0.004)。先前显示可以降低死亡率的γ辐射的启动剂量(0.5 mG​​y),对细胞对辐射的反应影响很小,并且不能防止骨骼结构的有害变化。骨髓移植使照射后的骨髓细胞密度,骨周转率和大多数骨结构指标正常化。总之,辐射诱导的骨髓细胞死亡与以下因素有关:1)骨形成的瞬时增加,至少部分是由于激活了骨衬细胞,以及2)由于破骨细胞周长的增加,导致骨吸收增加。骨髓移植可有效缓解急性暴露于高剂量全身γ射线对骨骼更新的不利影响。

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