Cohen Tatiana V, Klarmann Kimberly D, Sakchaisri Krisada, Cooper Jason P, Kuhns Douglas, Anver Miriam, Johnson Peter F, Williams Simon C, Keller Jonathan R, Stewart Colin L
Cancer and Developmental Biology Laboratory, CCR, Frederick, MD 21702, USA.
Hum Mol Genet. 2008 Oct 1;17(19):2921-33. doi: 10.1093/hmg/ddn191. Epub 2008 Jul 11.
The lamin B receptor (LBR) is an integral nuclear envelope protein that interacts with chromatin and has homology to sterol reductases. Mutations in LBR result in Pelger-Huët anomaly and HEM-Greenberg skeletal dysplasia, whereas in mice Lbr mutations result in ichthyosis. To further understand the function of the LBR and its role in disease, we derived a novel mouse model with a gene-trap insertion into the Lbr locus (Lbr(GT/GT)). Phenotypically, the Lbr(GT/GT) mice are similar to ichthyosis mice. The Lbr(GT/GT) granulocytes lack a mature segmented nucleus and have a block in late maturation. Despite these changes in nuclear morphology, the innate granulocyte immune function in the killing of Staphylococcus aureus bacteria appears to be intact. Granulocyte differentiation requires the transcription factor C/EBPepsilon. We identified C/EBPepsilon binding sites within the Lbr promoter and used EMSAs and luciferase assays to show that Lbr is transcriptionally regulated by C/EBPepsilon. Our findings indicate that the Lbr(GT/GT) mice are a model for Pelger-Huët anomaly and that Lbr, under transcriptional regulation of C/EBPepsilon, is necessary for morphological but not necessarily functional granulocyte maturation.
核纤层蛋白B受体(LBR)是一种整合于核膜的蛋白质,它与染色质相互作用,且与固醇还原酶具有同源性。LBR的突变会导致Pelger-Huët异常和HEM-格林伯格骨骼发育不良,而在小鼠中,Lbr突变会导致鱼鳞病。为了进一步了解LBR的功能及其在疾病中的作用,我们构建了一种新型小鼠模型,该模型在Lbr基因座上发生了基因陷阱插入(Lbr(GT/GT))。从表型上看,Lbr(GT/GT)小鼠与鱼鳞病小鼠相似。Lbr(GT/GT)粒细胞缺乏成熟的分叶核,且在后期成熟过程中受阻。尽管核形态发生了这些变化,但粒细胞在杀灭金黄色葡萄球菌方面的固有免疫功能似乎并未受损。粒细胞分化需要转录因子C/EBPε。我们在Lbr启动子内鉴定出C/EBPε结合位点,并通过电泳迁移率变动分析(EMSA)和荧光素酶测定表明Lbr受C/EBPε的转录调控。我们的研究结果表明,Lbr(GT/GT)小鼠是Pelger-Huët异常的模型,并且在C/EBPε的转录调控下,Lbr对于粒细胞的形态成熟是必需的,但对于其功能成熟不一定必需。