Wnt7b stimulates embryonic lung growth by coordinately increasing the replication of epithelium and mesenchyme

被引:122
作者
Rajagopal, Jayaraj [1 ,2 ,3 ]
Carroll, Thomas J. [4 ]
Guseh, J. Sawalla [1 ,2 ,3 ]
Bores, Sam A. [1 ,2 ]
Blank, Leah J. [1 ,2 ]
Anderson, William J. [1 ,2 ]
Yu, Jing [5 ]
Zhou, Qiao [1 ,2 ]
McMahon, Andrew P. [1 ]
Melton, Douglas A. [1 ,2 ]
机构
[1] Harvard Univ, Harvard Stem Cell Inst, Dept Mol & Cell Biol, Cambridge, MA 02138 USA
[2] Massachusetts Gen Hosp, Howard Hughes Med Inst, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Internal Med, Boston, MA 02114 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dept Internal Med, Dallas, TX 75390 USA
[5] Univ Virginia, Dept Cell Biol, Charlottesville, VA 22908 USA
来源
DEVELOPMENT | 2008年 / 135卷 / 09期
关键词
lung organogenesis; Wnt signaling; organ growth;
D O I
10.1242/dev.015495
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The effects of Wnt7b on lung development were examined using a conditional Wnt7b-null mouse. Wnt7b-null lungs are markedly hypoplastic, yet display largely normal patterning and cell differentiation. In contrast to findings in prior hypomorphic Wnt7b models, we find decreased replication of both developing epithelium and mesenchyme, without abnormalities of vascular smooth muscle development. We further demonstrate that Wnt7b signals to neighboring cells to activate both autocrine and paracrine canonical Wnt signaling cascades. In contrast to results from hypomorphic models, we show that Wnt7b modulates several important signaling pathways in the lung. Together, these cascades result in the coordinated proliferation of adjacent epithelial and mesenchymal cells to stimulate organ growth with few alterations in differentiation and patterning.
引用
收藏
页码:1625 / 1634
页数:10
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