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Publication : Use of hPSC-derived 3D organoids and mouse genetics to define the roles of YAP in the development of the esophagus.

First Author  Bailey DD Year  2019
Journal  Development Volume  146
Issue  23 PubMed ID  31748205
Mgi Jnum  J:293338 Mgi Id  MGI:6452665
Doi  10.1242/dev.178855 Citation  Bailey DD, et al. (2019) Use of hPSC-derived 3D organoids and mouse genetics to define the roles of YAP in the development of the esophagus. Development 146(23):dev178855
abstractText  Balanced progenitor activities are crucial for the development and maintenance of high turn-over organs such as the esophagus. However, the molecular mechanisms regulating these progenitor activities in the esophagus remain to be elucidated. Here, we demonstrated that Yap is required for the proliferation of esophageal progenitor cells (EPCs) in the developing murine esophagus. We found that Yap deficiency reduces EPC proliferation and stratification whereas persistent Yap activation increases cell proliferation and causes aberrant stratification of the developing esophagus. We further demonstrated that the role of YAP signaling is conserved in the developing human esophagus by utilizing 3D human pluripotent stem cell (hPSC)-derived esophageal organoid culture. Taken together, our studies combining loss/gain-of-function murine models and hPSC differentiation support a key role for YAP in the self-renewal of EPCs and stratification of the esophageal epithelium.
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