A Wnt/Notch/Pax7 signaling network supports tissue integrity in tongue development

• Published in: The Journal of biological chemistry Vol. 292; no. 22; pp. 9409 - 9419
• Main Authors: Zhu, Xiao-Jing, Yuan, Xueyan, Wang, Min, Fang, Yukun, Liu, Yudong, Zhang, Xiaoyun, Yang, Xueqin, Li, Yan, Li, Jianying, Li, Feixue, Dai, Zhong-Min, Qiu, Mengsheng, Zhang, Ze, Zhang, Zunyi
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 02.06.2017; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; connective tissue; craniofacial development; Developmental Biology; Epithelial Cells - metabolism; Humans; Mice; Mice, Knockout; mouse; muscle progenitor cells; myogenesis; Organ Specificity; PAX7 Transcription Factor - genetics; PAX7 Transcription Factor - metabolism; Receptors, Notch - genetics; Receptors, Notch - metabolism; Satellite Cells, Skeletal Muscle - metabolism; Tongue - embryology; Wnt signaling; Wnt Signaling Pathway - physiology; mouse; Wnt signaling; craniofacial development; myogenesis; connective tissue; muscle progenitor cells
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M117.789438

The tongue is one of the major structures involved in human food intake and speech. Tongue malformations such as aglossia, microglossia, and ankyloglossia are congenital birth defects, greatly affecting individuals' quality of life. However, the molecular basis of the tissue-tissue interactions that ensure tissue morphogenesis to form a functional tongue remains largely unknown. Here we show that ShhCre-mediated epithelial deletion of Wntless (Wls), the key regulator for intracellular Wnt trafficking, leads to lingual hypoplasia in mice. Disruption of epithelial Wnt production by Wls deletion in epithelial cells led to a failure in lingual epidermal stratification and loss of the lamina propria and the underlying superior longitudinal muscle in developing mouse tongues. These defective phenotypes resulted from a reduction in epithelial basal cells positive for the basal epidermal marker protein p63 and from impaired proliferation and differentiation in connective tissue and paired box 3 (Pax3)- and Pax7-positive muscle progenitor cells. We also found that epithelial Wnt production is required for activation of the Notch signaling pathway, which promotes proliferation of myogenic progenitor cells. Notch signaling in turn negatively regulated Wnt signaling during tongue morphogenesis. We further show that Pax7 is a direct Notch target gene in the embryonic tongue. In summary, our findings demonstrate a key role for the lingual epithelial signals in supporting the integrity of the lamina propria and muscular tissue during tongue development and that a Wnt/Notch/Pax7 genetic hierarchy is involved in this development.