| First Author | Suzuki A | Year | 2018 |
| Journal | Development | Volume | 145 |
| Issue | 23 | PubMed ID | 30389854 |
| Mgi Jnum | J:272614 | Mgi Id | MGI:6284212 |
| Doi | 10.1242/dev.168351 | Citation | Suzuki A, et al. (2018) WNT/beta-catenin signaling plays a crucial role in myoblast fusion through regulation of nephrin expression during development. Development 145(23):dev168351 |
| abstractText | Skeletal muscle development is controlled by a series of multiple orchestrated regulatory pathways. WNT/beta-catenin is one of the most important pathways for myogenesis; however, it remains unclear how this signaling pathway regulates myogenesis in a temporal- and spatial-specific manner. Here, we show that WNT/beta-catenin signaling is crucial for myoblast fusion through regulation of the nephrin (Nphs1) gene in the Myog-Cre-expressing myoblast population. Mice deficient for the beta-catenin gene in Myog-Cre-expressing myoblasts (Ctnnb1(F/F);Myog-Cre mice) displayed myoblast fusion defects, but not migration or cell proliferation defects. The promoter region of Nphs1 contains the conserved beta-catenin-binding element, and Nphs1 expression was induced by the activation of WNT/beta-catenin signaling. The induction of Nphs1 in cultured myoblasts from Ctnnb1(F/F);Myog-Cre mice restored the myoblast fusion defect, indicating that nephrin is functionally relevant in WNT/beta-catenin-dependent myoblast fusion. Taken together, our results indicate that WNT/beta-catenin signaling is crucial for myoblast fusion through the regulation of the Nphs1 gene. |
