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Figure 4


Fig. 4. Osx1-GFP::Cre removal of ß-catenin function results in a failure to develop terminally differentiated osteoblasts. (A-Q') Histological analysis and in situ hybridization of 35S-labeled riboprobes to sections of E18.5 tibia from (A-Q) ß-cateninc/n (wild type) and (A'-Q') Osx1-GFP::Cre;ß-cateninc/n (mutant) embryos. Specific anti-sense riboprobes were used that identify marker genes for: states of osteoblast and chondrocyte differentiation, (D,D') Col1{alpha}1, (E,E') Runx2, (F,F') osterix1, (G,G') osteocalcin, (H,H') Col2{alpha}1 and (I,I') Col10{alpha}1; components of Hh signaling, (J,J') Ihh and (K,K') Ptch1; components of canonical Wnt signaling, (L,L') Dkk1 and (M,M') Tcf1; the early osteoblast marker, (N,N') Bmp3; matrix remodeling, (O,O') Mmp9 and (P,P') Mmp13; and vascularization, (Q,Q') Vegf. Boxed areas in B and B' are presented at higher magnification in C and C', respectively. Black arrows indicate the absence of ossification in the mutant periosteum. White arrowheads indicate the invading wedge of mesenchymal cells into the marrow cavity, whereas black arrowheads indicate sites of ectopic expression of chondrocyte marker genes.





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