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

Author:

Rajagopal Jayaraj123,Carroll Thomas J.4,Guseh J. Sawalla123,Bores Sam A.12,Blank Leah J.12,Anderson William J.12,Yu Jing5,Zhou Qiao12,McMahon Andrew P.1,Melton Douglas A.12

Affiliation:

1. Department of Molecular and Cellular Biology, Harvard Stem Cell Institute,Harvard University, Cambridge, MA 02138, USA.

2. Howard Hughes Medical Institute, Massachusetts General Hospital, Boston, MA 02114, USA.

3. Department of Internal Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.

4. Department of Internal Medicine, Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

5. Department of Cell Biology, University of Virginia, Charlottesville, VA 22908,USA.

Abstract

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.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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