Department of Biochemistry and Molecular Biology, Monash University, Clayton VIC 3800, Australia.
Division of Molecular Genetics and Development, Institute for Molecular Bioscience, The University of Queensland, Brisbane QLD 4072, Australia.
Dev Cell. 2014 Apr 28;29(2):188-202. doi: 10.1016/j.devcel.2014.02.017.
Although kidneys of equal size can vary 10-fold in nephron number at birth, discovering what regulates such variation has been hampered by a lack of quantitative parameters defining kidney development. Here we report a comprehensive, quantitative, multiscale analysis of mammalian kidney development in which we measure changes in cell number, compartment volumes, and cellular dynamics across the entirety of organogenesis, focusing on two key nephrogenic progenitor populations: the ureteric epithelium and the cap mesenchyme. In doing so, we describe a discontinuous developmental program governed by dynamic changes in interactions between these key cellular populations occurring within a previously unappreciated structurally stereotypic organ architecture. We also illustrate the application of this approach to the detection of a subtle mutant phenotype. This baseline program of kidney morphogenesis provides a framework for assessing genetic and environmental developmental perturbation and will serve as a gold standard for the analysis of other organs.
尽管出生时大小相等的肾脏中肾单位数量可能相差 10 倍,但由于缺乏定量参数来定义肾脏发育,因此发现调节这种差异的因素受到了阻碍。在这里,我们报告了对哺乳动物肾脏发育的全面、定量、多尺度分析,其中我们测量了器官发生过程中细胞数量、隔室体积和细胞动力学的变化,重点关注两个关键的肾祖细胞群体:输尿管上皮和帽状间充质。通过这样做,我们描述了一个由这些关键细胞群体之间的相互作用的动态变化控制的不连续发育程序,这些变化发生在以前未被重视的结构上具有立体同型性的器官结构内。我们还说明了该方法在检测微妙的突变表型中的应用。这种肾脏形态发生的基本程序为评估遗传和环境发育干扰提供了一个框架,并将作为分析其他器官的黄金标准。