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通过神经生长因子诱导的NGFI-B核输出调节视黄酸信号传导。

Modulation of retinoid signalling through NGF-induced nuclear export of NGFI-B.

作者信息

Katagiri Y, Takeda K, Yu Z X, Ferrans V J, Ozato K, Guroff G

机构信息

Section on Growth Factors, NICHD, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Nat Cell Biol. 2000 Jul;2(7):435-40. doi: 10.1038/35017072.

Abstract

The retinoid-X receptor (RXR) regulates multiple hormonal pathways through heterodimerization with nuclear receptors such as the all-trans retinoic acid receptor (RAR). The orphan nuclear receptor NGFI-B (also called Nur77) can heterodimerize with RXR. Here we show that nerve growth factor (NGF) induces the phosphorylation of Ser 105 of NGFI-B in PC12 phaeochromocytoma cells, resulting in translocation of the NGFI-B-RXR heterodimer complex out of the nucleus using nuclear export signals within NGFI-B. As a consequence of the redistribution of RXR, the transcriptional activity of RXR-RAR is reduced. NGFI-B-mediated nuclear export of receptors may serve as a mechanism for crosstalk between NGF and retinoid pathways.

摘要

维甲酸X受体(RXR)通过与核受体如全反式维甲酸受体(RAR)异源二聚化来调节多种激素途径。孤儿核受体NGFI-B(也称为Nur77)可与RXR异源二聚化。在此我们表明,神经生长因子(NGF)在PC12嗜铬细胞瘤细胞中诱导NGFI-B的Ser 105磷酸化,导致NGFI-B-RXR异源二聚体复合物利用NGFI-B内的核输出信号从细胞核中转运出来。由于RXR的重新分布,RXR-RAR的转录活性降低。NGFI-B介导的受体核输出可能作为NGF和类维生素A途径之间相互作用的一种机制。

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