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胸部照射后大鼠肺组织中水通道蛋白1和5的表达

The expression of aquaporins 1 and 5 in rat lung after thoracic irradiation.

作者信息

Sun Cheng-Ying, Zhao Yu-Xia, Zhong Wen, Liu Da-Wei, Chen Yan-Zhi, Qin Li-Li, Bai Lu, Liu Dan

机构信息

Department of Radiation Oncology, The Fourth Affiliated Hospital of China Medical University, No. 4 Chongshan Road, Huanggu District, Shenyang 110032, China.

Department of Radiation Oncology, The Fourth Affiliated Hospital of China Medical University, No. 4 Chongshan Road, Huanggu District, Shenyang 110032, China

出版信息

J Radiat Res. 2014 Jul;55(4):683-9. doi: 10.1093/jrr/rru008. Epub 2014 Feb 24.

Abstract

Radiation-induced lung toxicity (RILT), leading to radiation pneumonia or fibrosis, is a primary problem of radiation therapy. The pathogenesis of RILT remains unclear. In this study, we used a rat model of RILT to examine the expression of aquaporins (AQPs) after radiation injury. Sprague Dawley rats were given a single dose of 17 Gy (dose rate of 3.0 Gy/min) of X-irradiation to the thorax. Rats that survived acute pneumonitis (at 1-4 weeks) were evaluated weekly for the expression of AQP1 and AQP5 in the lung by immunohistochemical and reverse transcription polymerase chain reaction (RT-PCR) analyses. Immunohistochemical analysis showed that AQP1 protein was expressed in the capillary endothelium, and its level was significantly decreased after irradiation. AQP5 protein was expressed in the alveolar epithelium, and its level was increased between Days 7 and 14 after irradiation but decreased at Day 28, compared with the sham group. The RT-PCR results were consistent with the immunohistochemical analysis results. In summary, this study provides the first report of AQP1 and AQP5 expression in a model of radiation-induced pulmonary inflammation and edema. Decreased levels of AQP1 and AQP5 after irradiation suggest that these proteins play a role in the pathogenesis of RILT.

摘要

放射性肺毒性(RILT)可导致放射性肺炎或肺纤维化,是放射治疗的一个主要问题。RILT的发病机制尚不清楚。在本研究中,我们使用RILT大鼠模型来检测辐射损伤后水通道蛋白(AQP)的表达。对Sprague Dawley大鼠胸部给予单次17 Gy(剂量率为3.0 Gy/min)的X射线照射。对在急性肺炎期存活(1 - 4周)的大鼠,通过免疫组织化学和逆转录聚合酶链反应(RT-PCR)分析,每周评估肺组织中AQP1和AQP5的表达。免疫组织化学分析显示,AQP1蛋白在毛细血管内皮中表达,照射后其水平显著降低。AQP5蛋白在肺泡上皮中表达,与假手术组相比,照射后第7至14天其水平升高,但在第28天降低。RT-PCR结果与免疫组织化学分析结果一致。总之,本研究首次报道了辐射诱导的肺部炎症和水肿模型中AQP1和AQP5的表达情况。照射后AQP1和AQP5水平降低表明这些蛋白在RILT的发病机制中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd49/4100000/44f9479863cd/rru00801.jpg

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