Singhal Sharad S, Yadav Sushma, Roth Cherice, Singhal Jyotsana
Department of Molecular Biology and Immunology, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Biochem Pharmacol. 2009 Mar 1;77(5):761-9. doi: 10.1016/j.bcp.2008.10.006. Epub 2008 Oct 15.
RLIP76, a stress-responsive, multi-functional protein with multi-specific transport activity towards glutathione-conjugates (GS-E) and chemotherapeutic agents, is frequently over-expressed in malignant cells. Our recent studies suggest that it plays a prominent anti-apoptotic role selectively in cancer cells. We have previously shown that RLIP76 accounts for up to 80% of the transport of GS-E and blocking the RLIP76-mediated transport of GS-E in cells results in the accumulation of pro-apoptotic endogenous electrophiles and on-set of apoptosis. Here we demonstrate that when RLIP76 mediate transport of GS-E is abrogated either by anti-RLIP76 IgG or accumulation of 4-hydroxynonenal (4-HNE) and its GSH-conjugate (GS-HNE) occurs and a massive apoptosis is observed in cells, indicate that the inhibition of RLIP76 transport activity at the cell surface is sufficient for observed anti-tumor activity. RLIP76 is linked with certain cellular functions including membrane plasticity and movement (as a primary 'effector' in the Ral pathway, perhaps functioning as a GTPase activating protein, or GAP), and as a component of clathrin-coated pit-mediated receptor-ligand endocytosis-a process that mediates movement of membrane vesicles.
RLIP76是一种应激反应性多功能蛋白,对谷胱甘肽偶联物(GS-E)和化疗药物具有多特异性转运活性,在恶性细胞中经常过度表达。我们最近的研究表明,它在癌细胞中选择性地发挥着显著的抗凋亡作用。我们之前已经表明,RLIP76占GS-E转运的80%,阻断细胞中RLIP76介导的GS-E转运会导致促凋亡内源性亲电试剂的积累和细胞凋亡的发生。在这里我们证明,当抗RLIP76 IgG或4-羟基壬烯醛(4-HNE)及其谷胱甘肽偶联物(GS-HNE)的积累消除了RLIP76介导的GS-E转运,并且在细胞中观察到大量细胞凋亡时,表明在细胞表面抑制RLIP76转运活性足以产生观察到的抗肿瘤活性。RLIP76与某些细胞功能相关,包括膜可塑性和运动(作为Ral途径中的主要“效应器”,可能作为一种GTP酶激活蛋白或GAP发挥作用),并且作为网格蛋白包被小窝介导的受体-配体内吞作用的一个组成部分——这一过程介导膜泡的运动。