Journal
DEVELOPMENT
Volume 145, Issue 23, Pages -Publisher
COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.168351
Keywords
WNT/beta-caten in signaling; Muscle development; Myoblast fusion; Nephrin
Categories
Funding
- National Institutes of Health
- National Institute of Dental and Craniofacial Research [DE024759, DE026208, DE026767, DE026509]
- NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH [R03DE026509, R03DE024759, R01DE026767, R03DE026208] Funding Source: NIH RePORTER
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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-Cm-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.
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