Irradiation induces a biphasic expression of pro-inflammatory cytokines in the lung

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Irradiation induces a biphasic expression of pro-inflammatory cytokines in the lung. / Rübe, Claudia E; Wilfert, Falk; Palm, Jan; König, Jochem; Burdak-Rothkamm, Susanne; Liu, Li; Schuck, Andreas; Willich, Normann; Rübe, Christian.

In: STRAHLENTHER ONKOL, Vol. 180, No. 7, 07.2004, p. 442-8.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Rübe, CE, Wilfert, F, Palm, J, König, J, Burdak-Rothkamm, S, Liu, L, Schuck, A, Willich, N & Rübe, C 2004, 'Irradiation induces a biphasic expression of pro-inflammatory cytokines in the lung', STRAHLENTHER ONKOL, vol. 180, no. 7, pp. 442-8. https://doi.org/10.1007/s00066-004-1265-7

APA

Rübe, C. E., Wilfert, F., Palm, J., König, J., Burdak-Rothkamm, S., Liu, L., Schuck, A., Willich, N., & Rübe, C. (2004). Irradiation induces a biphasic expression of pro-inflammatory cytokines in the lung. STRAHLENTHER ONKOL, 180(7), 442-8. https://doi.org/10.1007/s00066-004-1265-7

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Bibtex

@article{68d251b8b19a4ff78cd94fd064e92702,
title = "Irradiation induces a biphasic expression of pro-inflammatory cytokines in the lung",
abstract = "BACKGROUND AND PURPOSE: The precise pathophysiological mechanisms of radiation-induced lung injury are poorly understood, but have been shown to correlate with dysregulation of different cytokines. The purpose of this study was to evaluate the time course of the pro-inflammatory cytokines tumor necrosis factor-(TNF-)alpha, interleukin-(IL-)1alpha and IL-6 after whole-lung irradiation.MATERIAL AND METHODS: The thoraces of C57BL/6J mice were irradiated with 12 Gy. Treated and control mice were sacrificed at 0.5, 1, 3, 6, 12, 24, 48, 72 h, 1, 2, 4, 8, 16, and 24 weeks post irradiation (p. i.). Real-time multiplex RT-PCR (reverse transcriptase polmyerase chain reaction) was established to evaluate the expression of TNF-alpha, IL-1alpha and IL-6 in the lung tissue of the mice. For histological analysis, lung tissue sections were stained by hematoxylin and eosin.RESULTS: Multiplex RT-PCR analysis revealed a biphasic expression of these pro-inflammatory cytokines in the lung tissue after irradiation. After an initial increase at 1 h p. i. for TNF-alpha and at 6 h p. i. for IL-1alpha and IL-6, the mRNA expression of these pro-inflammatory cytokines returned to basal levels (48 h, 72 h, 1 week, 2 weeks p. i.). During the pneumonic phase, TNF-alpha, IL-1alpha and IL-6 were significantly elevated and revealed their maximum at 8 weeks p. i. Histopathologic evaluation of the lung sections obtained within 4 weeks p. i. revealed only minor lung damage in 5-30% of the lung tissue. By contrast, at 8, 16, and 24 weeks p. i., 70-90% of the lung tissue revealed histopathologically detectable organizing alveolitis.CONCLUSION: Irradiation induces a biphasic expression of pro-inflammatory cytokines in the lung. The initial transitory cytokine response occurred within the first hours after lung irradiation with no detectable histopathologic alterations. The second, more persistent cytokine elevation coincided with the onset of histologically discernible organizing acute pneumonitis.",
keywords = "Animals, Base Sequence, Cytokines/genetics, DNA Primers, Female, Inflammation/physiopathology, Lung/immunology, Mice, Mice, Inbred C57BL, Reverse Transcriptase Polymerase Chain Reaction",
author = "R{\"u}be, {Claudia E} and Falk Wilfert and Jan Palm and Jochem K{\"o}nig and Susanne Burdak-Rothkamm and Li Liu and Andreas Schuck and Normann Willich and Christian R{\"u}be",
year = "2004",
month = jul,
doi = "10.1007/s00066-004-1265-7",
language = "English",
volume = "180",
pages = "442--8",
journal = "STRAHLENTHER ONKOL",
issn = "0179-7158",
publisher = "Urban und Vogel",
number = "7",

}

RIS

TY - JOUR

T1 - Irradiation induces a biphasic expression of pro-inflammatory cytokines in the lung

AU - Rübe, Claudia E

AU - Wilfert, Falk

AU - Palm, Jan

AU - König, Jochem

AU - Burdak-Rothkamm, Susanne

AU - Liu, Li

AU - Schuck, Andreas

AU - Willich, Normann

AU - Rübe, Christian

PY - 2004/7

Y1 - 2004/7

N2 - BACKGROUND AND PURPOSE: The precise pathophysiological mechanisms of radiation-induced lung injury are poorly understood, but have been shown to correlate with dysregulation of different cytokines. The purpose of this study was to evaluate the time course of the pro-inflammatory cytokines tumor necrosis factor-(TNF-)alpha, interleukin-(IL-)1alpha and IL-6 after whole-lung irradiation.MATERIAL AND METHODS: The thoraces of C57BL/6J mice were irradiated with 12 Gy. Treated and control mice were sacrificed at 0.5, 1, 3, 6, 12, 24, 48, 72 h, 1, 2, 4, 8, 16, and 24 weeks post irradiation (p. i.). Real-time multiplex RT-PCR (reverse transcriptase polmyerase chain reaction) was established to evaluate the expression of TNF-alpha, IL-1alpha and IL-6 in the lung tissue of the mice. For histological analysis, lung tissue sections were stained by hematoxylin and eosin.RESULTS: Multiplex RT-PCR analysis revealed a biphasic expression of these pro-inflammatory cytokines in the lung tissue after irradiation. After an initial increase at 1 h p. i. for TNF-alpha and at 6 h p. i. for IL-1alpha and IL-6, the mRNA expression of these pro-inflammatory cytokines returned to basal levels (48 h, 72 h, 1 week, 2 weeks p. i.). During the pneumonic phase, TNF-alpha, IL-1alpha and IL-6 were significantly elevated and revealed their maximum at 8 weeks p. i. Histopathologic evaluation of the lung sections obtained within 4 weeks p. i. revealed only minor lung damage in 5-30% of the lung tissue. By contrast, at 8, 16, and 24 weeks p. i., 70-90% of the lung tissue revealed histopathologically detectable organizing alveolitis.CONCLUSION: Irradiation induces a biphasic expression of pro-inflammatory cytokines in the lung. The initial transitory cytokine response occurred within the first hours after lung irradiation with no detectable histopathologic alterations. The second, more persistent cytokine elevation coincided with the onset of histologically discernible organizing acute pneumonitis.

AB - BACKGROUND AND PURPOSE: The precise pathophysiological mechanisms of radiation-induced lung injury are poorly understood, but have been shown to correlate with dysregulation of different cytokines. The purpose of this study was to evaluate the time course of the pro-inflammatory cytokines tumor necrosis factor-(TNF-)alpha, interleukin-(IL-)1alpha and IL-6 after whole-lung irradiation.MATERIAL AND METHODS: The thoraces of C57BL/6J mice were irradiated with 12 Gy. Treated and control mice were sacrificed at 0.5, 1, 3, 6, 12, 24, 48, 72 h, 1, 2, 4, 8, 16, and 24 weeks post irradiation (p. i.). Real-time multiplex RT-PCR (reverse transcriptase polmyerase chain reaction) was established to evaluate the expression of TNF-alpha, IL-1alpha and IL-6 in the lung tissue of the mice. For histological analysis, lung tissue sections were stained by hematoxylin and eosin.RESULTS: Multiplex RT-PCR analysis revealed a biphasic expression of these pro-inflammatory cytokines in the lung tissue after irradiation. After an initial increase at 1 h p. i. for TNF-alpha and at 6 h p. i. for IL-1alpha and IL-6, the mRNA expression of these pro-inflammatory cytokines returned to basal levels (48 h, 72 h, 1 week, 2 weeks p. i.). During the pneumonic phase, TNF-alpha, IL-1alpha and IL-6 were significantly elevated and revealed their maximum at 8 weeks p. i. Histopathologic evaluation of the lung sections obtained within 4 weeks p. i. revealed only minor lung damage in 5-30% of the lung tissue. By contrast, at 8, 16, and 24 weeks p. i., 70-90% of the lung tissue revealed histopathologically detectable organizing alveolitis.CONCLUSION: Irradiation induces a biphasic expression of pro-inflammatory cytokines in the lung. The initial transitory cytokine response occurred within the first hours after lung irradiation with no detectable histopathologic alterations. The second, more persistent cytokine elevation coincided with the onset of histologically discernible organizing acute pneumonitis.

KW - Animals

KW - Base Sequence

KW - Cytokines/genetics

KW - DNA Primers

KW - Female

KW - Inflammation/physiopathology

KW - Lung/immunology

KW - Mice

KW - Mice, Inbred C57BL

KW - Reverse Transcriptase Polymerase Chain Reaction

U2 - 10.1007/s00066-004-1265-7

DO - 10.1007/s00066-004-1265-7

M3 - SCORING: Journal article

C2 - 15241532

VL - 180

SP - 442

EP - 448

JO - STRAHLENTHER ONKOL

JF - STRAHLENTHER ONKOL

SN - 0179-7158

IS - 7

ER -