Department of Biochemistry, School of Medicine, Stanford University, Stanford, CA 94305, USA.
Dev Cell. 2012 Sep 11;23(3):482-93. doi: 10.1016/j.devcel.2012.07.009.
Some of the most serious diseases involve altered size and structure of the arterial wall. Elucidating how arterial walls are built could aid understanding of these diseases, but little is known about how concentric layers of muscle cells and the outer adventitial layer are assembled and patterned around endothelial tubes. Using histochemical, clonal, and genetic analysis in mice, here we show that the pulmonary artery wall is constructed radially, from the inside out, by two separate but coordinated processes. One is sequential induction of successive cell layers from surrounding mesenchyme. The other is controlled invasion of outer layers by inner layer cells through developmentally regulated cell reorientation and radial migration. We propose that a radial signal gradient controls these processes and provide evidence that PDGF-B and at least one other signal contribute. Modulation of such radial signaling pathways may underlie vessel-specific differences and pathological changes in arterial wall size and structure.
一些最严重的疾病涉及动脉壁大小和结构的改变。阐明动脉壁是如何构建的,可以帮助我们理解这些疾病,但对于围绕内皮管的同心层的肌肉细胞和外层的外膜是如何组装和形成模式的,我们知之甚少。在这里,我们使用小鼠的组织化学、克隆和遗传分析表明,肺动脉壁是从内到外呈放射状构建的,这是由两个独立但协调的过程完成的。一个是从周围间充质连续诱导连续的细胞层。另一个是内层细胞通过发育调节的细胞重定向和径向迁移,受控地侵入外层。我们提出,一个放射状信号梯度控制这些过程,并提供证据表明 PDGF-B 和至少另一个信号起作用。这种放射状信号通路的调节可能是血管特异性差异和动脉壁大小和结构病理变化的基础。