High-resolution gene expression analysis of the developing mouse kidney defines novel cellular compartments within the nephron progenitor population

被引:134
作者
Mugford, Joshua W. [1 ]
Yu, Jing [1 ]
Kobayashi, Akio [1 ]
McMahon, Andrew P. [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
Cap mesenchyme; Metanephros; Kidney; Progenitor; Transcription factor; Nephrogenesis; MAMMALIAN KIDNEY; METANEPHRIC KIDNEY; INTERMEDIATE MESODERM; SIGNALING PATHWAY; TUBULE FORMATION; BETA-CATENIN; WNT PATHWAY; MORPHOGENESIS; NEPHROGENESIS; MESENCHYME;
D O I
10.1016/j.ydbio.2009.06.043
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The functional unit of the kidney is the nephron. During its organogenesis, the mammalian metanephric kidney generates thousands of nephrons over a protracted period of fetal life. All nephrons are derived from a population of self-renewing multi-potent progenitor cells, termed the cap mesenchyme. However, our understanding of the molecular and cellular mechanisms underlying nephron development is at an early stage. In order to identify factors involved in nephrogenesis, we performed a high-resolution, spatial pro. ling of a number of transcriptional regulators expressed within the cap mesenchyme and early developing nephron. Our results demonstrate novel, stereotypic, spatially defined cellular sub-domains within the cap mesenchyme, which may, in part, reflect induction of nephron precursors. These results suggest a hitherto unappreciated complexity of cell states that accompany the assembly of the metanephric kidney, likely reflecting diverse regulatory actions such as the maintenance and induction of nephron progenitors. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:312 / 323
页数:12
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