Hiramatsu Nobuhiko, Kasai Ayumi, Du Shuqi, Takeda Masayuki, Hayakawa Kunihiro, Okamura Maro, Yao Jian, Kitamura Masanori
Department of Molecular Signaling, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi 409-3898, Japan.
FEBS Lett. 2007 May 15;581(10):2055-9. doi: 10.1016/j.febslet.2007.04.040. Epub 2007 Apr 25.
Endoplasmic reticulum (ER) stress-responsive alkaline phosphatase (ES-TRAP) serves as a sensitive indicator for ER stress. In response to heavy metals including cadmium, nickel and cobalt, hepatocytes and renal tubular cells expressing ES-TRAP exhibited ER stress and decreased ES-TRAP activity. In ES-TRAP transgenic mice, acute exposure to cadmium showed rapid, transient decreases in the activity of serum ES-TRAP. It was inversely correlated with the induction of endogenous ER stress markers in the liver and kidney. Our result provides first evidence for the acute, reversible induction of ER stress in vivo after exposure to heavy metal.
内质网(ER)应激反应性碱性磷酸酶(ES-TRAP)是内质网应激的敏感指标。在对包括镉、镍和钴在内的重金属作出反应时,表达ES-TRAP的肝细胞和肾小管细胞会出现内质网应激,且ES-TRAP活性降低。在ES-TRAP转基因小鼠中,急性镉暴露导致血清ES-TRAP活性迅速、短暂下降。这与肝脏和肾脏中内源性内质网应激标志物的诱导呈负相关。我们的结果首次证明了暴露于重金属后体内内质网应激的急性、可逆诱导。