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本文引用的文献

1
Hepatocyte proliferation and hepatomegaly induced by phenobarbital and 1,4-bis [2-(3,5-dichloropyridyloxy)] benzene is suppressed in hepatocyte-targeted glypican 3 transgenic mice.肝靶向聚糖蛋白 3 转基因小鼠中苯巴比妥和 1,4-双[2-(3,5-二氯吡啶氧基)]苯诱导的肝细胞增殖和肝肿大受到抑制。
Hepatology. 2011 Aug;54(2):620-30. doi: 10.1002/hep.24417.
2
Selective phthalate activation of naturally occurring human constitutive androstane receptor splice variants and the pregnane X receptor.选择性邻苯二甲酸酯激活天然存在的人组成型雄烷受体剪接变异体和孕烷 X 受体。
Toxicol Sci. 2011 Apr;120(2):381-91. doi: 10.1093/toxsci/kfq394. Epub 2011 Jan 12.
3
Pregnane X receptor PXR activates the GADD45beta gene, eliciting the p38 MAPK signal and cell migration.孕烷 X 受体(PXR)激活 GADD45β 基因,引发 p38 MAPK 信号和细胞迁移。
J Biol Chem. 2011 Feb 4;286(5):3570-8. doi: 10.1074/jbc.M110.179812. Epub 2010 Dec 2.
4
SnapShot: NR coregulators.简讯:核共调节因子
Cell. 2010 Oct 1;143(1):172-172.e1. doi: 10.1016/j.cell.2010.09.032.
5
Suppression of liver regeneration and hepatocyte proliferation in hepatocyte-targeted glypican 3 transgenic mice.肝靶向聚糖蛋白 3 转基因小鼠中肝再生和肝细胞增殖的抑制。
Hepatology. 2010 Sep;52(3):1060-7. doi: 10.1002/hep.23794.
6
Enhanced liver regeneration following changes induced by hepatocyte-specific genetic ablation of integrin-linked kinase.整合素连接激酶肝细胞特异性基因敲除诱导的变化后肝脏再生增强。
Hepatology. 2009 Sep;50(3):844-51. doi: 10.1002/hep.23059.
7
Di(2-ethylhexyl) phthalate is a highly potent agonist for the human constitutive androstane receptor splice variant CAR2.邻苯二甲酸二(2-乙基己基)酯是一种对人组成型雄烷受体剪接变体CAR2具有高度活性的激动剂。
Mol Pharmacol. 2009 May;75(5):1005-13. doi: 10.1124/mol.108.053702. Epub 2009 Feb 11.
8
Bioactive terpenoids and flavonoids from Ginkgo biloba extract induce the expression of hepatic drug-metabolizing enzymes through pregnane X receptor, constitutive androstane receptor, and aryl hydrocarbon receptor-mediated pathways.银杏叶提取物中的生物活性萜类化合物和黄酮类化合物通过孕烷X受体、组成型雄甾烷受体和芳烃受体介导的途径诱导肝药代谢酶的表达。
Pharm Res. 2009 Apr;26(4):872-82. doi: 10.1007/s11095-008-9788-8. Epub 2008 Nov 26.
9
The balance of reproducibility, sensitivity, and specificity of lists of differentially expressed genes in microarray studies.微阵列研究中差异表达基因列表的可重复性、敏感性和特异性之间的平衡。
BMC Bioinformatics. 2008 Aug 12;9 Suppl 9(Suppl 9):S10. doi: 10.1186/1471-2105-9-S9-S10.
10
GADD45B inhibits MKK7-induced cardiac hypertrophy and the polymorphisms of GADD45B is associated with inter-ventricular septum hypertrophy.生长停滞和DNA损伤诱导蛋白45β(GADD45B)抑制MKK7诱导的心肌肥大,且GADD45B的多态性与室间隔肥厚相关。
Biochem Biophys Res Commun. 2008 Aug 8;372(4):623-8. doi: 10.1016/j.bbrc.2008.05.122. Epub 2008 Jun 2.

Gadd45β 是一种诱导型转录共激活因子,可促进小鼠肝脏的快速生长。

Gadd45β is an inducible coactivator of transcription that facilitates rapid liver growth in mice.

机构信息

Department of Pathology and Marion Bessin Liver Center, Albert Einstein College of Medicine, New York, New York, USA.

出版信息

J Clin Invest. 2011 Nov;121(11):4491-502. doi: 10.1172/JCI38760. Epub 2011 Oct 3.

DOI:10.1172/JCI38760
PMID:21965327
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3204825/
Abstract

The growth arrest and DNA damage-inducible 45 (Gadd45) proteins act in many cellular processes. In the liver, Gadd45b (encoding Gadd45β) is the gene most strongly induced early during both compensatory regeneration and drug-induced hyperplasia. The latter response is associated with the dramatic and rapid hepatocyte growth that follows administration of the xenobiotic TCPOBOP (1,4-bis[2-(3,5)-dichoropyridyloxy] benzene), a ligand of the nuclear receptor constitutive androstane receptor (CAR). Here, we have shown that Gadd45b-/- mice have intact proliferative responses following administration of a single dose of TCPOBOP, but marked growth delays. Moreover, early transcriptional stimulation of CAR target genes was weaker in Gadd45b-/- mice than in wild-type animals, and more genes were downregulated. Gadd45β was then found to have a direct role in transcription by physically binding to CAR, and TCPOBOP treatment caused both proteins to localize to a regulatory element for the CAR target gene cytochrome P450 2b10 (Cyp2b10). Further analysis defined separate Gadd45β domains that mediated binding to CAR and transcriptional activation. Although baseline hepatic expression of Gadd45b was broadly comparable to that of other coactivators, its 140-fold stimulation by TCPOBOP was striking and unique. The induction of Gadd45β is therefore a response that facilitates increased transcription, allowing rapid expansion of liver mass for protection against xenobiotic insults.

摘要

生长停滞和 DNA 损伤诱导蛋白 45(Gadd45)在许多细胞过程中发挥作用。在肝脏中,Gadd45b(编码 Gadd45β)是在代偿性再生和药物诱导的增生过程中早期最强诱导的基因。后者与随后给予外源性毒物 TCPOBOP(1,4-双[2-(3,5)-二氯吡啶氧基]苯)时发生的剧烈和快速的肝细胞生长有关,TCPOBOP 是核受体组成型雄烷受体(CAR)的配体。在这里,我们已经表明,Gadd45b-/- 小鼠在给予单次 TCPOBOP 剂量后具有完整的增殖反应,但生长明显延迟。此外,Gadd45b-/- 小鼠中 CAR 靶基因的早期转录刺激比野生型动物弱,并且更多基因被下调。Gadd45β 然后通过与 CAR 物理结合而具有直接的转录作用,并且 TCPOBOP 处理导致两种蛋白质定位于 CAR 靶基因细胞色素 P450 2b10(Cyp2b10)的调节元件。进一步的分析确定了介导与 CAR 结合和转录激活的 Gadd45β 分离结构域。尽管 Gadd45b 的基础肝表达与其他共激活因子广泛可比,但它被 TCPOBOP 强烈刺激 140 倍是惊人且独特的。因此,Gadd45β 的诱导是一种促进转录增加的反应,允许快速扩大肝质量以保护免受外源性毒物的侵害。