Morriss-Kay G M, Iseki S, Johnson D
Department of Human Anatomy and Genetics, University of Oxford, South Parks Road, Oxford OX1 3QX, UK.
Novartis Found Symp. 2001;232:102-16; discussion 116-21. doi: 10.1002/0470846658.ch8.
Activating mutations of genes encoding the transmembrane tyrosine kinase receptors fibroblast growth factor receptors (FGFRs)1-3, and haploinsufficiency of the transcription factor TWIST, cause human craniosynostosis syndromes that typically involve the coronal suture. We have investigated the functional roles of these genes in development of the coronal suture in mouse fetuses, and tested the effects of increasing FGFR signalling by applying exogenous FGF2 to the suture. The results indicate that the proliferation-differentiation balance in normal sutural development involves a gradient of extracellular FGF from the region of differentiation, in which Fgfr1 is expressed, to the sutural mesenchyme, in which low levels of FGF are associated with Fgfr2 expression in osteogenic stem cells. Experimental increase of sutural FGF levels leads to down-regulation of Fgfr2, up-regulation of Fgfr1, up-regulation of the osteogenic differentiation gene Osteopontin, and cessation of proliferation. Twist is expressed in the midsutural mesenchyme and is partially co-expressed with Fgfr2, consistent with the possibility that it is involved in maintaining proliferation through regulating transcription of Fgfr2.
编码跨膜酪氨酸激酶受体成纤维细胞生长因子受体(FGFRs)1 - 3的基因激活突变,以及转录因子TWIST的单倍体不足,会导致人类颅缝早闭综合征,该综合征通常累及冠状缝。我们研究了这些基因在小鼠胎儿冠状缝发育中的功能作用,并通过向缝中施加外源性FGF2来测试增加FGFR信号传导的影响。结果表明,正常缝发育中的增殖 - 分化平衡涉及从表达Fgfr1的分化区域到缝间充质的细胞外FGF梯度,在缝间充质中,低水平的FGF与成骨干细胞中的Fgfr2表达相关。实验性增加缝中FGF水平会导致Fgfr2下调、Fgfr1上调、成骨分化基因骨桥蛋白上调以及增殖停止。Twist在缝间中胚层表达,并与Fgfr2部分共表达,这与它可能通过调节Fgfr2转录来维持增殖的可能性一致。