Schumann R R
Max-Delbrück-Centrum für Molekulare Medizin (MDC), Robert-Rössle-Cancer Center, University Hospital Rudolf-Virchow, Free University of Berlin, Germany.
Prog Clin Biol Res. 1995;392:297-304.
The Lipopolysaccharide Binding Protein (LBP) is of high importance for endotoxin recognition, presentation and subsequent cytokine induction in immune cells. LBP, which is a member of a growing family of structurally and functionally related proteins, is synthesized in hepatocytes and secreted into the blood stream constitutively. During the acute phase response, however, LBP levels rise substantially and here the mechanisms of induction of LBP protein synthesis were reviewed. The induction of LBP in hepatocytes is due to transcriptional and posttranscriptional mechanisms as we have shown by nuclear run-on and RNA half-life experiments. Cloning of the 5'-flanking region of the LBP gene, furthermore revealed a typical acute phase protein promoter. Reporter gene assays employing the luciferase gene and mutation variants of the LBP promoter revealed that integrity of a common acute phase promoter motif, named APRE/STAT-3 is essential for activation of the LBP promoter. Elucidation of the transcriptional activation mechanism could point the way to a therapeutically lowering of LBP levels in high risk patients for reducing their susceptibility to Gram-negative septic shock.
脂多糖结合蛋白(LBP)对于免疫细胞中内毒素的识别、呈递以及随后的细胞因子诱导具有高度重要性。LBP是结构和功能相关蛋白不断增加的家族中的一员,由肝细胞合成并持续分泌到血流中。然而,在急性期反应期间,LBP水平大幅升高,在此对LBP蛋白合成的诱导机制进行了综述。正如我们通过细胞核连续转录和RNA半衰期实验所表明的,肝细胞中LBP的诱导是由于转录和转录后机制。此外,LBP基因5'侧翼区的克隆揭示了一个典型的急性期蛋白启动子。使用荧光素酶基因和LBP启动子突变变体的报告基因检测表明,一个名为APRE/STAT-3的常见急性期启动子基序的完整性对于LBP启动子的激活至关重要。转录激活机制的阐明可能为降低高危患者的LBP水平以降低其对革兰氏阴性败血症休克的易感性指明治疗方向。