Liu B, Lee H Y, Weinzimer S A, Powell D R, Clifford J L, Kurie J M, Cohen P
Department of Pediatrics, University of California, Los Angeles, California 90095-1752, USA.
J Biol Chem. 2000 Oct 27;275(43):33607-13. doi: 10.1074/jbc.M002547200.
Insulin-like growth factor-binding protein (IGFBP)-3 regulates apoptosis in an IGF-independent fashion and has been shown to localize to nuclei. We cloned the nuclear receptor retinoid X receptor-alpha(RXR-alpha) as an IGFBP-3 protein partner in a yeast two-hybrid screen. Multiple methodologies showed that IGFBP-3 and RXR-alpha bind each other within the nucleus. IGFBP-3-induced apoptosis was abolished in RXR-alpha-knockout cells. IGFBP-3 and RXR ligands were additive in inducing apoptosis in prostate cancer cells. IGFBP-3 enhanced RXR response element and inhibited RARE signaling. Thus, RXR-alpha-IGFBP-3 interaction leads to modulation of the transcriptional activity of RXR-alpha and is essential for mediating the effects of IGFBP-3 on apoptosis.
胰岛素样生长因子结合蛋白(IGFBP)-3以不依赖胰岛素样生长因子(IGF)的方式调节细胞凋亡,并且已被证明定位于细胞核。我们在酵母双杂交筛选中克隆了核受体维甲酸X受体α(RXR-α)作为IGFBP-3的蛋白伴侣。多种方法表明IGFBP-3和RXR-α在细胞核内相互结合。在RXR-α基因敲除细胞中,IGFBP-3诱导的细胞凋亡被消除。IGFBP-3和RXR配体在诱导前列腺癌细胞凋亡方面具有相加作用。IGFBP-3增强了RXR反应元件并抑制了视黄酸反应元件(RARE)信号传导。因此,RXR-α与IGFBP-3的相互作用导致RXR-α转录活性的调节,并且对于介导IGFBP-3对细胞凋亡的作用至关重要。