Malhotra Vivek, Eaves-Pyles Tonyia, Odoms Kelli, Quaid Gina, Shanley Thomas P, Wong Hector R
Division of Critical Care Medicine, Children's Hospital Medical Center and Children's Hospital Research Foundation, Cincinnati, Ohio 45229-3039, USA.
Biochem Biophys Res Commun. 2002 Mar 1;291(3):453-7. doi: 10.1006/bbrc.2002.6470.
The heat shock response is known to inhibit NF-kappaB activation and NF-kappaB-dependent gene expression. Herein we determined if cells lacking heat shock factor-1 (HSF-1), the major transcription factor regulating heat shock protein gene expression, have an altered ability to modulate NF-kappaB activation. Embryonic fibroblasts from HSF-1-null mutant mice (HSF-1-/- cells) had a drastically reduced ability to express heat shock protein-70 in response to heat shock, compared to embryonic fibroblasts from wild-type mice (HSF+/+ cells). There was no difference, however, in the ability of heat shock to inhibit TNFalpha-mediated NF-kappaB activation, IkappaBalpha degradation, IkappaB kinase activation, and macrophage chemotactic protein-1 expression in the HSF-1-/- cells compared to the HSF-1+/+ cells. These data demonstrate that heat shock inhibits activation of the NF-kappaB/IkappaBalpha pathway and NF-kappaB-dependent gene expression in the absence of an intact heat shock response.
已知热休克反应可抑制核因子κB(NF-κB)的激活及NF-κB依赖的基因表达。在此,我们确定了缺乏热休克因子1(HSF-1)(调节热休克蛋白基因表达的主要转录因子)的细胞调节NF-κB激活的能力是否发生改变。与野生型小鼠的胚胎成纤维细胞(HSF+/+细胞)相比,HSF-1基因敲除突变小鼠的胚胎成纤维细胞(HSF-1-/-细胞)在热休克反应时表达热休克蛋白70的能力大幅降低。然而,与HSF-1+/+细胞相比,热休克抑制HSF-1-/-细胞中肿瘤坏死因子α(TNFα)介导的NF-κB激活、IκBα降解、IκB激酶激活及巨噬细胞趋化蛋白-1表达的能力并无差异。这些数据表明,在缺乏完整热休克反应的情况下,热休克可抑制NF-κB/IκBα信号通路的激活及NF-κB依赖的基因表达。