Journal List > Tuberc Respir Dis > v.67(1) > 1001404

Choi, Rho, Jang, Lee, Lee, Koh, Kim, Kim, Kim, and Lee: Biphasic Increase of Pro-inflammatory Cytokines in Mice Lung after Irradiation

Abstract

Background

The pathophysiologic mechanisms of radiation-induced lung injury should be elucidated to enhance the therapeutic efficacy of radiotherapy and to manage patients exposed to serious radiation by accident. It has been suggested that pro-inflammatory cytokines play an important role in radiation-induced effect on the lung. This study was aimed to investigate changes in pro-inflammatory cytokines such as TNF-α, MIP-2, IL-1β and HMGB1, a newly recognized inflammatory mediator.

Methods

The chests of BALB/c mice were selectively irradiated with single fraction of 20 Gy and then sacrificed at indicated times. Pathologic changes in the lung were examined after H&E staining. The expression level of pro-inflammatory cytokines was evaluated by ELISA kits in lung homogenate and in serum.

Results

Radiation induced inflammatory changes and mild fibrosis in lung. Biphasic increase of TNF-α and IL-1β was found in lung homogenate at 4 hours and at 3 weeks after radiation. The elevation in the second phase tended to be more intense. However, there was no similar change in serum. MIP-2 level was slightly increased in lung homogenate at 4 hours, but not at 3 weeks. HMGB1 was increased at 3 weeks in serum while there was no significant change in lung homogenate.

Conclusion

Radiation induced a biphasic increase in TNF-α and IL-1β. The effective control of second phase cytokine elevation should contribute to preventing severe lung fibrosis caused by radiation.

Figures and Tables

Figure 1
Histologic changes of lung parenchyma at 4 h (A), 2 wk (B), and 8 wk (C) after 20 Gy irradiation. (A) Peri-vascular edema and an increased interstitial cellularity due to exudative neutrophilic infiltration in interstitial vascular spaces were found. (B) Lymphocytic collectons were noted in the interstitium with no evidence of fibrosis 2 weeks after irradiation. (C) Alveolar spaces were distorted by mild fibrosis and inflammatory infiltration was persistent (H&E stain, ×200).
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Figure 2
Biphasic increase of cytokines in lung after irradiation. The level of TNF-α (A), MIP-2 (B) and IL-1β (C) in ling homogenates was determined by ELISA kits at the indicated time after irradiation. Each experimental group consisted of 3 mice.
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Figure 3
The expression level of HMGB1 did not change in lung parenchyma after irradiation. The amount of HMGB1 in the lung was examined by Western blot analysis (A). The expression level of HMGB1 was also evaluated by ELISA kits in lung homogenate (B) and serum (C) at the indicated times after irradiation. Each experimental group consisted of 3 mice.
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