Early changes in lung gene expression due to high tidal volume

被引:124
作者
Copland, IB
Kavanagh, BP
Engelberts, D
McKerlie, C
Belik, J
Post, M
机构
[1] Hosp Sick Children, Lung Biol Program, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Dept Crit Care Med, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Dept Lab Med, Toronto, ON, Canada
[4] Univ Toronto, Dept Pathobiol, Toronto, ON, Canada
[5] Univ Toronto, Dept Pediat, Toronto, ON, Canada
关键词
ventilation; gene expression profiling;
D O I
10.1164/rccm.200208-964OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
The purpose of this study was to use gene expression profiling to understand how adult rat lung responds to high tidal volume (HV) ventilation in vivo. HV ventilation for 30 minutes did not cause discernable lung injury (in terms of altered mechanics or histology) but caused obvious injury when continued for 90 minutes. However, at 30-minute ventilation, HV caused significant upregulation of 10 genes and suppression of 12 genes. Among the upregulated genes were transcription factors, stress proteins, and inflammatory mediators; the downregulated genes were exemplified by metabolic regulatory genes. On the basis of cluster analysis, we studied Egr-1, c-Jun, heat shock protein 70, and interleukin (IL)-1beta in further detail. Temporal studies demonstrated that Egr-1 and c-lun were increased early and before heat shock protein 70 and IL-1beta. Spatial studies using in situ hybridization and laser capture microscopy revealed that all four genes were upregulated primarily in the bronchiolar airway epithelium. Furthermore, at 90 minutes of HV ventilation, a significant increase in intracellular IL-1beta protein was observed. Although there are limitations to gene array methodology, the current data suggest a global hypothesis that (1) the effects of HV are cumulative; (2) specific patterns of gene activation and suppression precede lung injury; and (3) alteration of gene expression after mechanical stretch is pathogenic.
引用
收藏
页码:1051 / 1059
页数:9
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