Muenke syndrome mutation,FgfR3 P244R,Causes TMJ Defects

Muenke syndrome is characterized by various craniofacial deformities and is caused by an autosomal-dominant activating mutation in fibroblast growth factor receptor 3 (fgfr3 p250r). here,using mice carrying a corresponding mutation (fgfr3 p244r),we determined whether the mutation affects temporomandibular joint (tmj) development and growth. in situ hybridization showed that fgfr3 was expressed in condylar chondroprogenitors and maturing chondrocytes that also expressed the indian hedgehog (ihh) receptor and transcriptional target patched 1(ptch1). in fgfr3 p244r mutants,the condyles displayed reduced levels of ihh expression,h4c-positive proliferating chondroprogenitors,and collagen type ii- and type x-expressing chondrocytes. primary bone spongiosa formation was also disturbed and was accompanied by increased osteoclastic activity and reduced trabecular bone formation. treatment of wild-type condylar explants with recombinant fgf2/fgf9 decreased ptch1 and pthrp expression in superficial/polymorphic layers and proliferation in chondroprogenitors. we also observed early degenerative changes of condylar articular cartilage,abnormal development of the articular eminence/glenoid fossa in the tmj,and fusion of the articular disc. analysis of our data indicates that the activating fgfr3 p244r mutation disturbs tmj developmental processes,likely by reducing hedgehog signaling and endochondral ossification. we suggest that a balance between fgf and hedgehog signaling pathways is critical for the integrity of tmj development and for the maintenance of cellular organization. © 2012 international & american associations for dental research.