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

被引:165
作者
Katagiri, Y
Takeda, K
Yu, ZX
Ferrans, VJ
Ozato, K
Guroff, G
机构
[1] NICHD, Growth Factors Sect, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Pathol Sect, NIH, Bethesda, MD 20892 USA
[3] NICHD, Lab Mol Growth Regulat, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1038/35017072
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:435 / 440
页数:6
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