Suppr超能文献

枯否细胞缺失对肝窦内皮细胞的辐射防护作用。

Radioprotective effect of kupffer cell depletion on hepatic sinusoidal endothelial cells.

作者信息

Chen Yi-Xing, Zeng Zhao-Chong, Sun Jing, Zhang Zhen-Yu, Zeng Hai-Ying, Hu Wei-Xu

机构信息

a  Department of Radiation Oncology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.

出版信息

Radiat Res. 2015 May;183(5):563-70. doi: 10.1667/RR13869.1. Epub 2015 Apr 21.

Abstract

Radiation-induced liver injury remains a clinical problem and data suggest that sinusoidal endothelial cells (SECs) are an important target. The purpose of this study was to determine whether the inhibition of Kupffer cells before exposure would protect SECs from radiation-induced injury. Sprague-Dawley rats were intravenously injected 24 h before irradiation with Kupffer cell inhibitor gadolinium chloride (GdCl3) (10 mg/kg body weight). Three groups of animals were treated: 1. control group (saline and sham irradiation); 2. GdCl3 + 30 Gy radiation group and 3. 30 Gy radiation only group. Specimens were collected at 2, 6, 12, 24 and 48 h after completion of each treatment. Liver tissue was assessed for inflammatory cytokine expression and radiation-induced SEC injury based on serum hyaluronic acid (HA) level, apoptosis and ultrastructural and histological analyses. The results showed that radiation exposure caused apoptosis of SECs, but not hepatocytes. Inflammatory cytokine expression, including tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) expression, was significantly attenuated in the GdCl3 + 30 Gy radiation group, compared with the 30 Gy radiation-only group (P < 0.05). The GdCl3 + radiation-treated rats exhibited significantly lower levels of HA and SEC apoptosis than the radiation-treated only rats at early time points, and radiation-induced liver injury was also attenuated. In conclusion, we hypothesize that selective Kupffer cell inhibition by gadolinium chloride was shown to reduce apoptosis in SECs caused by irradiation of the live and protected the liver against radiation-induced injury.

摘要

放射性肝损伤仍是一个临床问题,数据表明肝血窦内皮细胞(SECs)是一个重要靶点。本研究的目的是确定在暴露前抑制库普弗细胞是否能保护SECs免受辐射诱导的损伤。在照射前24小时,给Sprague-Dawley大鼠静脉注射库普弗细胞抑制剂氯化钆(GdCl3)(10mg/kg体重)。对三组动物进行治疗:1. 对照组(生理盐水和假照射);2. GdCl3 + 30Gy辐射组和3. 仅30Gy辐射组。在每次治疗完成后的2、6、12、24和48小时收集标本。基于血清透明质酸(HA)水平、凋亡以及超微结构和组织学分析,评估肝组织中的炎性细胞因子表达和辐射诱导的SECs损伤。结果表明,辐射暴露导致SECs凋亡,但未导致肝细胞凋亡。与仅30Gy辐射组相比,GdCl3 + 30Gy辐射组中包括肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)表达在内的炎性细胞因子表达显著减弱(P < 0.05)。在早期时间点,GdCl3 + 辐射处理的大鼠的HA水平和SECs凋亡水平显著低于仅辐射处理的大鼠,并且辐射诱导的肝损伤也有所减轻。总之,我们推测氯化钆对库普弗细胞的选择性抑制作用可减少肝脏照射引起的SECs凋亡,并保护肝脏免受辐射诱导的损伤。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验