| First Author | Tan Y | Year | 2016 |
| Journal | Biochem Biophys Res Commun | Volume | 475 |
| Issue | 4 | Pages | 308-14 |
| PubMed ID | 27221046 | Mgi Jnum | J:235953 |
| Mgi Id | MGI:5804048 | Doi | 10.1016/j.bbrc.2016.05.101 |
| Citation | Tan Y, et al. (2016) ADAM10 is essential for cranial neural crest-derived maxillofacial bone development. Biochem Biophys Res Commun 475(4):308-14 |
| abstractText | Growth disorders of the craniofacial bones may lead to craniofacial deformities. The majority of maxillofacial bones are derived from cranial neural crest cells via intramembranous bone formation. Any interruption of the craniofacial skeleton development process might lead to craniofacial malformation. A disintegrin and metalloprotease (ADAM)10 plays an essential role in organ development and tissue integrity in different organs. However, little is known about its function in craniofacial bone formation. Therefore, we investigated the role of ADAM10 in the developing craniofacial skeleton, particularly during typical mandibular bone development. First, we showed that ADAM10 was expressed in a specific area of the craniofacial bone and that the expression pattern dynamically changed during normal mouse craniofacial development. Then, we crossed wnt1-cre transgenic mice with adam10-flox mice to generate ADAM10 conditional knockout mice. The stereomicroscopic, radiographic, and von Kossa staining results showed that conditional knockout of ADAM10 in cranial neural crest cells led to embryonic death, craniofacial dysmorphia and bone defects. Furthermore, we demonstrated that impaired mineralization could be triggered by decreased osteoblast differentiation, increased cell death. Overall, these findings show that ADAM10 plays an essential role in craniofacial bone development. |
