The bronchiolar epithelium as a prominent source of pro-inflammatory cytokines after lung irradiation

被引:104
作者
Rübe, CE
Uthe, D
Wilfert, F
Ludwig, D
Yang, KY
König, J
Palm, J
Schuck, A
Willich, N
Remberger, K
Rübe, C
机构
[1] Univ Saarland, Dept Radiotherapy & Radiooncol, D-66421 Homburg, Germany
[2] Univ Saarland, Dept Pathol, D-66421 Homburg, Germany
[3] Univ Saarland, Inst Med Biometr Epidemiol & Med Informat, D-66421 Homburg, Germany
[4] Univ Munster, Dept Radiotherapy & Radiooncol, D-4400 Munster, Germany
[5] Huazhong Univ Sci & Technol, Union Hosp Tongji Med Coll, Ctr Canc, Wuhan 430074, Peoples R China
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2005年 / 61卷 / 05期
关键词
TNF-alpha; IL-1; alpha; IL-6; pneumonitis; bronchiolar epithelium; ionizing radiation;
D O I
10.1016/j.ijrobp.2004.12.072
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To study in detail the temporal and spatial release of the pro-inflammatory cytokines tumor necrosis factor a, interleukin (IL)-1 alpha, and IL-6 in the lung tissue of C57BL/6 mice after thoracic irradiation with 12 Gy. Methods and Materials: C57BL/6J mice were exposed to either sham irradiation or a single fraction of 12 Gy delivered to the thorax. Treated and sham-irradiated control mice were killed at 0.5 h, 1 h, 3 h, 6 h, 12 h, 24 h, 48 h, 72 h, 1 week, 2 weeks, 4 weeks, 8 weeks, 16 weeks, and 24 weeks post-irradiation (p.i.). Real-time multiplex reverse transcriptase polymerase chain reaction was established to evaluate the relative messenger RNA (mRNA) expression of TNF-alpha, IL-1 alpha, and IL-6 in the lung tissue of the mice (compared with nonirradiated lung tissue). Immunohistochemical detection methods (alkaline phosphatase anti-alkaline phosphatase, avidin-biotin-complex [ABC]) and automated image analysis were used to quantify the protein expression of TNF-alpha, IL-1 alpha, and IL-6 in the lung tissue (percentage of the positively stained area). Results: Radiation-induced release of the proinflammatory cytokines TNF-alpha, IL-1 alpha, and IL-6 in the lung tissue was detectable within the first hours after thoracic irradiation. We observed statistically significant up-regulations for TNF-alpha at 1 h p.i. on mRNA (4.99 +/- 1.60) and at 6 h p.i. on protein level (7.23% +/- 1.67%), for IL-1 alpha at 6 It p.i. on mRNA (11.03 +/- 0.77) and at 12 h p.i. on protein level (27.58% +/- 11.06%), for IL-6 at 6 It p.i. on mRNA (6.0 +/- 3.76) and at 12 h p.i. on protein level (7.12% +/- 1.93%). With immunohistochemistry, we could clearly demonstrate that the bronchiolar epithelium is the most prominent source of these inflammatory cytokines in the first hours after lung irradiation. During the stage of acute pneumonitis, the bronchiolar epithelium, as well as inflammatory cells in the lung interstitium, produced high amounts of TNF-alpha (with the maximal value at 4 weeks p.i.: 9.47% +/- 1.78 %), IL-1 alpha (with the peak value at 8 weeks p.i.: 14.76% +/- 7.77%), and IL-6 (with the peak value at 8 weeks p.i.: 4.28% +/- 1.33%). Conclusions: In the present study we have clearly demonstrated the immediate expression of the pro-inflammatory cytokines TNF-alpha, IL-1 alpha, and IL-6 in the bronchiolar epithelium in the first hours after lung irradiation. A second, long-lasting release of these cytokines by the bronchiolar and alveolar epithelium, as well as by inflammatory cells, was observed at the onset of acute pneumonitis. Therefore, we postulate that lung irradiation causes immediate epithelial reaction, with the bronchiolar epithelium becoming a significant source of proinflammatory cytokines capable of promoting inflammation through recruitment and activation of inflammatory cells. (c) 2005 Elsevier Inc.
引用
收藏
页码:1482 / 1492
页数:11
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