Department of Pharmaceutics and Therapeutics, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan; Laboratory of Pharmaceutics, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan.
Department of Pharmaceutics and Therapeutics, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan.
Biochem Biophys Res Commun. 2014 Jul 18;450(1):476-81. doi: 10.1016/j.bbrc.2014.05.146. Epub 2014 Jun 9.
Recently, we found that albumin overload induces expression of the transcription factor hypoxia-inducible factor-1α (HIF-1α) protein and several HIF-1 target genes in human renal proximal tubular epithelial cell line HK-2. In this study, the role of albumin-bound fatty acids in the albumin-induced HIF-1 activation was studied. The enhancing effect of fatty acid-bearing human serum albumin [FA(+)HSA] treatment on HIF-1α protein expression was much greater than that of fatty acid-depleted human serum albumin [FA(-)HSA] treatment. The FA(+)HSA treatment induced HIF-1 target gene mRNAs such as those of glucose transporter 1 (GLUT1), glyceraldehyde 3-phosphate dehydrogenase (GAPDH), and breast cancer resistance protein (BCRP) in concentration-dependent manners, while FA(-)HSA caused no significant increases in these mRNAs. Consistent with increased GLUT1 mRNA, GLUT1 protein expression and GLUT inhibitor cytochalasin B-sensitive d-[(3)H]glucose uptake activity were significantly enhanced by treatment with FA(+)HSA, but not with FA(-)HSA. These findings indicate that fatty acids bound to albumin play a crucial role in albumin-induced HIF-1 activation followed by changes in HIF-1 target gene expression and protein product activity.
最近,我们发现白蛋白过载会诱导人肾近端小管上皮细胞系 HK-2 中转录因子缺氧诱导因子-1α(HIF-1α)蛋白和几种 HIF-1 靶基因的表达。在这项研究中,研究了白蛋白结合脂肪酸在白蛋白诱导的 HIF-1 激活中的作用。载脂肪酸人血清白蛋白 [FA(+)HSA]处理对 HIF-1α 蛋白表达的增强作用远大于脂肪酸耗尽人血清白蛋白 [FA(-)HSA]处理。FA(+)HSA 处理以浓度依赖性方式诱导 HIF-1 靶基因 mRNA 的表达,如葡萄糖转运蛋白 1(GLUT1)、甘油醛 3-磷酸脱氢酶(GAPDH)和乳腺癌耐药蛋白(BCRP),而 FA(-)HSA 则不会引起这些 mRNA 的显著增加。与 GLUT1 mRNA 的增加一致,GLUT1 蛋白表达和 GLUT 抑制剂细胞松弛素 B 敏感的 d-[(3)H]葡萄糖摄取活性均显著增强,而 FA(-)HSA 则没有。这些发现表明,与白蛋白结合的脂肪酸在白蛋白诱导的 HIF-1 激活及其后 HIF-1 靶基因表达和蛋白产物活性的改变中起关键作用。