Department of Biochemistry and Medical Chemistry, University of Pécs, Pécs, Hungary.
FEBS Lett. 2010 Jul 2;584(13):2953-60. doi: 10.1016/j.febslet.2010.05.027.
We found that overexpression of tail interacting protein of 47 kDa (TIP47), but not its truncated form (t-TIP47) protected NIH3T3 cells from hydrogen-peroxide-induced cell death, prevented the hydrogen-peroxide-induced mitochondrial depolarization determined by 5,50,6,60-tetrachloro-1,10,3,30-tetraethyl-benzimidazolylcarbocyanine iodide (JC1), while suppression of TIP47 in HeLa cells facilitated oxidative-stress-induced cell death. TIP47 was located to the cytoplasm of untreated cells, but some was associated to mitochondria in oxidative stress. Recombinant TIP47, but not t-TIP47 increased the mitochondrial membrane potential (Deltapsi), and partially prevented Ca2+ induced depolarization. It is assumed that TIP47 can bind to mitochondria in oxidative stress, and inhibit mitochondria mediated cell death by protecting mitochondrial membrane integrity.
我们发现,47kDa 尾相互作用蛋白(TIP47)的过表达,而不是其截断形式(t-TIP47),可保护 NIH3T3 细胞免受过氧化氢诱导的细胞死亡,防止由 5,50,6,60-四氯-1,10,3,30-四乙基苯并咪唑基羰花青碘(JC1)测定的过氧化氢诱导的线粒体去极化,而在 HeLa 细胞中抑制 TIP47 促进氧化应激诱导的细胞死亡。TIP47 位于未处理细胞的细胞质中,但在氧化应激中与线粒体有些关联。重组 TIP47,但不是 t-TIP47,增加了线粒体膜电位(Deltapsi),并部分防止了 Ca2+ 诱导的去极化。据推测,TIP47 可以在氧化应激时与线粒体结合,并通过保护线粒体膜完整性来抑制线粒体介导的细胞死亡。