Pathology Department, Stony Brook University, Stony Brook, NY 11794-8691, USA.
Pathology Department, Stony Brook University, Stony Brook, NY 11794-8691, USA; Department of Applied Radiation and Isotopes, Faculty of Sciences, Kasetsart University, Chatuchuck, Bangkok 10900, Thailand.
Life Sci Space Res (Amst). 2018 May;17:83-90. doi: 10.1016/j.lssr.2018.04.001. Epub 2018 Apr 19.
Little is known about plasma proteins that can be used as biomarkers for early and late responses to radiation. The purpose of this study was to determine a link between depletion of plasma gelsolin (pGSN) and cell-death as well as inflammatory responses in the lung (one of the tissues known to be radiosensitive) of the same exposed CBA/CaJ mice after exposure to heavy silicon (Si) ions. To prevent the development of multiple organ dysfunctions, pGSN (an important component of the extracellular actin-scavenging system) is responsible for the removal of actin that is released into the circulation during inflammation and from dying cells. We evaluated the levels of pGSN in plasma collected from groups of mice (5 mice in each) at 1 week (wk) and 1 month (1 mo) after exposure whole body to different doses of Si ions, i.e. 0, 0.1, 0.25, or 0.5 Gy (2 fractionated exposures, 15 days apart that totaled each selected dose). In the same mouse, the measurements of pGSN levels were coupled with the quantitation of injuries in the lung, determined by (a) the levels of cleaved poly (ADP-ribose) polymerase (cleaved-PARP), a marker of apoptotic cell-death, (b) the levels of activated nuclear factor-kappa B (NF-κB) and selected cytokines, i.e. tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), and IL-6, from tissue-lysates of the lung. Further, the ratio of neutrophils and lymphocytes (N/L) was determined in the same mouse. Our data indicated: (i) the magnitude of pGSN depletion was dependent to radiation dose at both harvest times, (ii) a persistent depletion of pGSN up to 1 mo post-exposure to 0.25 or 0.5 Gy of Si ions, (iii) an inverse-correlation between pGSN depletion and increased levels of cleaved-PARP, including activated NF-κB/pro-inflammatory cytokines in the lung, and (iv) at both harvest times, statistically significant increases in the N/L ratio in groups of mice exposed to 0.5 Gy only. Our findings suggested that depletion in pGSN levels reflects not only the responses to Si-ion exposure at both harvest times but also early and late-occurring damage.
关于可作为早期和晚期辐射反应生物标志物的血浆蛋白知之甚少。本研究的目的是确定暴露于重硅(Si)离子后,CBA/CaJ 小鼠的同一辐射敏感组织之一的肺中,血浆中格尔森(pGSN)耗竭与细胞死亡和炎症反应之间的联系。为了防止多器官功能障碍的发展,pGSN(细胞外肌动蛋白清除系统的重要组成部分)负责清除在炎症和死亡细胞中释放到循环中的肌动蛋白。我们评估了从暴露于不同剂量 Si 离子(0、0.1、0.25 或 0.5 Gy(2 次分割暴露,间隔 15 天,总计每个选定剂量)的全身的各组小鼠(每组 5 只)血浆中 pGSN 的水平1 周(wk)和 1 个月(1 mo)后。在同一只小鼠中,pGSN 水平的测量与肺损伤的定量相结合,通过(a)被切割的多聚(ADP-核糖)聚合酶(切割-PARP)的水平确定,这是细胞凋亡死亡的标志物,(b)核因子-kappa B(NF-κB)的水平和选定的细胞因子,即肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6,从肺组织的组织裂解物中确定。此外,还确定了同一小鼠中性粒细胞和淋巴细胞(N/L)的比值。我们的数据表明:(i)在两个收获时间,pGSN 耗竭的程度取决于辐射剂量,(ii)在暴露于 0.25 或 0.5 Gy Si 离子后 1 个月内持续耗尽 pGSN,(iii)pGSN 耗竭与肺中增加的切割-PARP 水平之间呈负相关,包括激活的 NF-κB/促炎细胞因子,以及(iv)在两个收获时间,仅暴露于 0.5 Gy 的小鼠组中,N/L 比值均显著增加。我们的发现表明,pGSN 水平的降低不仅反映了两次收获时对 Si 离子暴露的反应,还反映了早期和晚期发生的损伤。