The Hippo pathway effector YAP is an essential regulator of ductal progenitor patterning in the mouse submandibular gland

被引:36
作者
Szymaniak, Aleksander D. [1 ]
Mi, Rongjuan [1 ,2 ]
McCarthy, Shannon E. [1 ]
Gower, Adam C. [3 ]
Reynolds, Taylor L. [4 ]
Mingueneau, Michael [4 ]
Kukuruzinska, Maria [2 ]
Varelas, Xaralabos [1 ]
机构
[1] Boston Univ, Sch Med, Dept Biochem, Boston, MA USA
[2] Boston Univ, Sch Med, Dept Mol & Cell Biol, Boston, MA USA
[3] Boston Univ, Clin & Translat Sci Inst, Boston, MA 02215 USA
[4] Biogen, Immunol Res, Cambridge, MA USA
来源
ELIFE | 2017年 / 6卷
关键词
SALIVARY-GLAND; BRANCHING MORPHOGENESIS; EPITHELIAL PROGENITORS; CELL PROLIFERATION; SIGNALING PATHWAY; SJOGRENS-SYNDROME; TUMOR-SUPPRESSOR; STEM-CELLS; TGF-BETA; EXPRESSION;
D O I
10.7554/eLife.23499
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Salivary glands, such as submandibular glands (SMGs), are composed of branched epithelial ductal networks that terminate in acini that together produce, transport and secrete saliva. Here, we show that the transcriptional regulator Yap, a key effector of the Hippo pathway, is required for the proper patterning and morphogenesis of SMG epithelium. Epithelial deletion of Yap in developing SMGs results in the loss of ductal structures, arising from reduced expression of the EGF family member Epiregulin, which we show is required for the expansion of Krt5/Krt14-positive ductal progenitors. We further show that epithelial deletion of the Lats1 and Lats2 genes, which encode kinases that restrict nuclear Yap localization, results in morphogenesis defects accompanied by an expansion of Krt5/Krt14-positive cells. Collectively, our data indicate that Yap induced Epiregulin signaling promotes the identity of SMG ductal progenitors and that removal of nuclear Yap by Lats1/2-mediated signaling is critical for proper ductal maturation.
引用
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页数:23
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