Müller U, Wang D, Denda S, Meneses J J, Pedersen R A, Reichardt L F
Department of Physiology, University of California, San Francisco 94143, USA.
Cell. 1997 Mar 7;88(5):603-13. doi: 10.1016/s0092-8674(00)81903-0.
We present genetic evidence that integrins regulate epithelial-mesenchymal interactions during organogenesis. Mice with a mutation in the alpha8 gene do not express the integrin alpha8 beta1 and exhibit profound deficits in kidney morphogenesis. In wild-type animals, inductive interactions between the ureteric epithelium and metanephric mesenchyme are essential for kidney morphogenesis. In alpha8 mutant homozygotes, growth and branching of the ureteric bud and recruitment of mesenchymal cells into epithelial structures are defective. Consistent with these phenotypes, alpha8 expression is induced in mesenchymal cells upon contact with the ureter. Since none of its previously identified ligands appears likely to mediate the essential functions of alpha8 beta1 in kidney morphogenesis, we have used an alpha8 beta1-alkaline phosphatase chimera to localize novel ligand(s) in the growing ureter. The distribution of these ligand(s) makes them strong candidates for regulators of kidney morphogenesis.
我们提供了遗传学证据,表明整合素在器官发生过程中调节上皮-间充质相互作用。α8基因发生突变的小鼠不表达整合素α8β1,并且在肾脏形态发生方面表现出严重缺陷。在野生型动物中,输尿管上皮与后肾间充质之间的诱导性相互作用对于肾脏形态发生至关重要。在α8突变纯合子中,输尿管芽的生长和分支以及间充质细胞募集到上皮结构中存在缺陷。与这些表型一致,间充质细胞在与输尿管接触后会诱导α8表达。由于其先前鉴定的配体似乎都不太可能介导α8β1在肾脏形态发生中的重要功能,我们使用了α8β1-碱性磷酸酶嵌合体来定位正在生长的输尿管中的新型配体。这些配体的分布使其成为肾脏形态发生调节因子的有力候选者。