Mendelsohn Cathy
Department of Urology, Columbia University, New York, New York 10032, USA.
J Clin Invest. 2006 Mar;116(3):635-7. doi: 10.1172/JCI27985.
Radial patterning in the urinary tract and gut depends on reciprocal signaling between epithelial cells, which form mucosa, and mesenchyme, which forms smooth muscle and connective tissue. These interactions depend on sonic hedgehog (Shh), which is secreted by epithelial cells and induces expression of bone morphogenetic protein 4 (Bmp4), a signaling molecule required for differentiation of smooth muscle progenitors. Patterning of the specialized mucosa lining the anterior-posterior (A-P) axis may be controlled independently by regionally expressed mesenchymal transcription factors. A study by Airik et al. in this issue of the JCI reveals that T-box 18 (Tbx18), a transcription factor selectively expressed in ureteral mesenchyme, regulates smooth muscle differentiation by maintaining Shh1 responsiveness in mesenchymal progenitors (see the related article beginning on page 663). Deletion of Tbx18 resulted in defective urothelial differentiation at the level of the ureter, suggesting that Tbx18 acts via mesenchyme as an important regulator of A-P patterning in the urinary tract.
泌尿道和肠道的径向模式形成依赖于上皮细胞(形成黏膜)与间充质(形成平滑肌和结缔组织)之间的相互信号传导。这些相互作用依赖于音猬因子(Shh),它由上皮细胞分泌并诱导骨形态发生蛋白4(Bmp4)的表达,Bmp4是平滑肌祖细胞分化所需的信号分子。沿前后(A-P)轴排列的特殊黏膜的模式形成可能由区域表达的间充质转录因子独立控制。Airik等人在本期《临床研究杂志》上发表的一项研究表明,T-box 18(Tbx18)是一种在输尿管间充质中选择性表达的转录因子,它通过维持间充质祖细胞对Shh的反应性来调节平滑肌分化(见第663页开始的相关文章)。Tbx18的缺失导致输尿管水平的尿路上皮分化缺陷,这表明Tbx18通过间充质作为泌尿道A-P模式形成的重要调节因子发挥作用。