Department of Pathology and Marion Bessin Liver Center, Albert Einstein College of Medicine, New York, New York, USA.
J Clin Invest. 2011 Nov;121(11):4491-502. doi: 10.1172/JCI38760. Epub 2011 Oct 3.
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.
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。