Bergwerff M, Gittenberger-de Groot A C, DeRuiter M C, van Iperen L, Meijlink F, Poelmann R E
Department of Anatomy and Embryology, Leiden University Medical Centre, The Netherlands.
Dev Dyn. 1998 Sep;213(1):59-70. doi: 10.1002/(SICI)1097-0177(199809)213:1<59::AID-AJA6>3.0.CO;2-X.
PRX1 (MHox) and PRX2 (S8) were previously shown to be expressed throughout embryogenesis in complex, mostly mesenchyme-specific patterns. In the developing cardiovascular system both genes were highly expressed in prospective connective tissues, that is, endocardial cushions and valves, the epicardium, and the wall of the great arteries and veins. We further scrutinised expression of PRX1 and PRX2 in the developing vascular system of the chicken embryo and compared patterns with those of established vascular differentiation markers (muscle-actin, procollagen I, and fibrillin-2). PRX1 and PRX2 expression were associated with the primary vessel wall from early stages onward and became increasingly restricted to the adventitial and outer medial cell layers. PRX1 eventually colocalised strikingly with procollagen I and fibrillin-2 expression and generally excluded high smooth muscle actin expression. Furthermore, PRX1 expression preceded the segregation of very distinct nonmuscular cells and smooth muscle cells in the media of the great arteries. PRX2 patterns deviated at later stages from those of PRX1 and showed specific and high transcript levels in the ductus arteriosus from embryonic day 6 onward. Results suggest that PRX genes are not essential in smooth muscle contractile differentiation, but may be involved in matrix modulation in the vascular system and possibly in defining the noncontractile cellular phenotype and in media-adventitia definition.
PRX1(MHox)和PRX2(S8)先前已被证明在整个胚胎发生过程中以复杂的、主要是间充质特异性的模式表达。在发育中的心血管系统中,这两个基因在前体结缔组织中高表达,即心内膜垫和瓣膜、心外膜以及大动脉和静脉壁。我们进一步研究了PRX1和PRX2在鸡胚发育中的血管系统中的表达,并将其模式与已确定的血管分化标志物(肌动蛋白、I型前胶原和原纤蛋白-2)的模式进行了比较。从早期开始,PRX1和PRX2的表达就与初级血管壁相关,并越来越局限于外膜和外中膜细胞层。PRX1最终与I型前胶原和原纤蛋白-2的表达显著共定位,并且通常排除高平滑肌肌动蛋白表达。此外,PRX1的表达先于大动脉中膜中非常不同的非肌肉细胞和平滑肌细胞的分离。PRX2的模式在后期与PRX1的模式不同,并且从胚胎第6天开始在动脉导管中显示出特定的高转录水平。结果表明,PRX基因在平滑肌收缩分化中并非必不可少,但可能参与血管系统中的基质调节,并可能参与定义非收缩性细胞表型和中膜-外膜的界定。