Nugent P, Greene R M
Department of Biological and Biophysical Sciences, University of Louisville School of Dentistry, Kentucky 40292, USA.
In Vitro Cell Dev Biol Anim. 1998 Nov-Dec;34(10):831-5. doi: 10.1007/s11626-998-0038-5.
The palatal cleft seen in Msx-1 knock-out mice suggests a role for this gene in normal palate development. The cleft is presumed secondary to tooth and jaw malformations, since in situ hybridization suggests that Msx-1 mRNA is not highly expressed in developing palatal tissue. In this study we demonstrate, by Northern blot analysis, the expression of Msx-1, but not Msx-2, in the developing palate and in primary cultures of murine embryonic palate mesenchymal cells. Furthermore, we propose a role for Msx-1 in retinoic acid-induced cleft palate, since retinoic acid inhibits Msx-1 mRNA expression in palate mesenchymal cells. We also demonstrate that transforming growth factor beta inhibits Msx-1 mRNA expression in palate mesenchymal cells, with retinoic acid and transforming growth factor beta acting synergistically when added simultaneously to these cells. These data suggest a mechanistic interaction between retinoic acid, transforming growth factor beta, and Msx-1 in the etiology of retinoic acid-induced cleft palate.
在Msx-1基因敲除小鼠中观察到的腭裂表明该基因在正常腭部发育中发挥作用。这种腭裂被认为是牙齿和颌骨畸形的继发性结果,因为原位杂交显示Msx-1 mRNA在发育中的腭部组织中表达不高。在本研究中,我们通过Northern印迹分析证明,Msx-1在发育中的腭部以及小鼠胚胎腭间充质细胞的原代培养物中表达,但Msx-2不表达。此外,我们提出Msx-1在维甲酸诱导的腭裂中发挥作用,因为维甲酸抑制腭间充质细胞中Msx-1 mRNA的表达。我们还证明,转化生长因子β抑制腭间充质细胞中Msx-1 mRNA的表达,当维甲酸和转化生长因子β同时添加到这些细胞中时,它们具有协同作用。这些数据表明维甲酸、转化生长因子β和Msx-1在维甲酸诱导的腭裂病因中存在机制上的相互作用。