Group II phospholipase A(2) gene expression is transcriptionally regulated in rat liver during sepsis

被引:18
作者
Dong, LW [1 ]
Yang, J [1 ]
Tong, LJ [1 ]
Hsu, HK [1 ]
Liu, MS [1 ]
机构
[1] ST LOUIS UNIV, SCH MED, DEPT PHARMACOL & PHYSIOL SCI, ST LOUIS, MO 63104 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1997年 / 273卷 / 03期
关键词
transcriptional regulation; hepatic dysfunction; septic shock;
D O I
10.1152/ajpgi.1997.273.3.G706
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Changes in group II phospholipase A(2) (PLA(2)) gene expression in rat liver during different phases of sepsis were studied. Sepsis was induced by cecal ligation and puncture (CLP). The results show that PLA(2) activity was increased by 41 and 92% during early hyperdynamic phase (9 h after CLP) and late hypodynamic phase (18 h after CLP) of sepsis, respectively. Western blot analysis reveals that group II PLA(2) protein levels were elevated by 53 and 95% during early and late sepsis, respectively. Northern blot analysis depicts that the steady-state levels of group II PLA(2) mRNA were enhanced by 39 and 114% during early and late sepsis, respectively. Nuclear run-off assay shows that the transcription rates of group II PLA(2) gene transcript were stimulated by 36 and 74% during early and late sepsis, respectively. The actinomycin D pulse chase study indicates that the half-life of group II PLA(2) mRNA remained unaffected during early and late phases of sepsis. These results demonstrate that group II PLA(2) gene transcripts were overexpressed in rat liver during the progression of sepsis and that the overexpression was a result of the enhanced synthesis of group II PLA(2) mRNA. Because PLA(2) plays an important role in the maintenance of cell membrane integrity, our findings may contribute to the understanding of the pathogenesis of hepatic dysfunction during the progression of sepsis.
引用
收藏
页码:G706 / G712
页数:7
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