Identification of a Multipotent Self-Renewing Stromal Progenitor Population during Mammalian Kidney Organogenesis

被引:174
作者
Kobayashi, Akio [1 ,2 ,3 ]
Mugford, Joshua W. [1 ]
Krautzberger, A. Michaela [1 ,4 ]
Naiman, Natalie [2 ]
Liao, Jessica [2 ]
McMahon, Andrew P. [1 ,3 ,4 ]
机构
[1] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med,Renal Div, Boston, MA 02115 USA
[3] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[4] Univ So Calif, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, WM Keck Sch Med, Dept Stem Cell Biol & Regenerat Med, Los Angeles, CA 90089 USA
关键词
GENE-EXPRESSION; BRANCHING MORPHOGENESIS; MESENCHYME; CELLS; DIFFERENTIATION; SEGMENTATION; PRECURSOR; CATENIN; DEFINES; ATLAS;
D O I
10.1016/j.stemcr.2014.08.008
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The mammalian kidney is a complex organ consisting of multiple cell types. We previously showed that the Six2-expressing cap mesenchyme is a multipotent self-renewing progenitor population for the main body of the nephron, the basic functional unit of the kidney. However, the cellular mechanisms establishing stromal tissues are less clear. We demonstrate that the Foxd1-expressing cortical stroma represents a distinct multipotent self-renewing progenitor population that gives rise to stromal tissues of the interstitium, mesangium, and pericytes throughout kidney organogenesis. Fate map analysis of Foxd1-expressing cells demonstrates that a small subset of these cells contributes to Six2-expressing cells at the early stage of kidney outgrowth. Thereafter, there appears to be a strict nephron and stromal lineage boundary derived from Six2-expressing and Foxd1-expressing cell types, respectively. Taken together, our observations suggest that distinct multipotent self-renewing progenitor populations coordinate cellular differentiation of the nephron epithelium and renal stroma during mammalian kidney organogenesis.
引用
收藏
页码:650 / 662
页数:13
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