Defining a mesenchymal progenitor niche at single-cell resolution

被引:100
|
作者
Kumar, Maya E. [1 ,2 ]
Bogard, Patrick E. [1 ,2 ]
Espinoza, F. Hernan [1 ,2 ]
Menke, Douglas B. [1 ,3 ,4 ]
Kingsley, David M. [1 ,4 ]
Krasnow, Mark A. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
[3] Univ Georgia, Dept Genet, Athens, GA 30602 USA
[4] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
关键词
SMOOTH-MUSCLE; STEM-CELLS; INTESTINAL CRYPT; LUNG DEVELOPMENT; SELF-RENEWAL; POPULATIONS; HOMEOSTASIS; CONTRIBUTE; PROGRAM; GENE;
D O I
10.1126/science.1258810
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Most vertebrate organs are composed of epithelium surrounded by support and stromal tissues formed from mesenchyme cells, which are not generally thought to form organized progenitor pools. Here, we use clonal cell labeling with multicolor reporters to characterize individual mesenchymal progenitors in the developing mouse lung. We observe a diversity of mesenchymal progenitor populations with different locations, movements, and lineage boundaries. Airway smooth muscle (ASM) progenitors map exclusively to mesenchyme ahead of budding airways. Progenitors recruited from these tip pools differentiate into ASM around airway stalks; flanking stalk mesenchyme can be induced to form an ASM niche by a lateral bud or by an airway tip plus focal Wnt signal. Thus, mesenchymal progenitors can be organized into localized and carefully controlled domains that rival epithelial progenitor niches in regulatory sophistication.
引用
收藏
页码:827 / +
页数:10
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