A non-canonical JAGGED1 signal to JAK2 mediates osteoblast commitment in cranial neural crest cells.

ABSTRACT: During craniofacial development, cranial neural crest (CNC) cells migrate into the developing face and form bone through intramembranous ossification. Loss of JAGGED1 (JAG1) signaling in the CNC cells is associated with maxillary hypoplasia or maxillary bone deficiency (MBD) in mice and recapitulates the MBD seen in humans with Alagille syndrome. JAGGED1, a membrane-bound NOTCH ligand, is required for normal craniofacial development, and Jagged1 mutations in humans are known to cause Alagille Syndrome, which is associated with cardiac, biliary, and bone phenotypes and these children experience increased bony fractures. Previously, we demonstrated deficient maxillary osteogenesis in Wnt1-cre;Jagged1^f/f (Jag1CKO) mice by conditional deletion of Jagged1 in maxillary CNC cells. In t

SUBMITTER: Kamalakar A 

PROVIDER: S-EPMC6420215 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature