(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)
Click on image to view larger version.

Fig. 5. Analysis of chick frontal bone development with the RISAP
replication-incompetent virus. (A-F) Viral injections into
condensations in areas `I' and `II' (dark red spots) labeled large portions of
the developing frontal bone (A,D), with cells contributing to the anterior (B)
and posterior (E) halves of the frontal bone, respectively. Expansion of the
two condensations results in a relatively sharp boundary between the anterior
and posterior parts, but no suture forms (arrowheads; C,F). Notice that cells
from the anterior condensation contribute to the more posterior part (C).
(G-L) Skeletal phenotypes in frontal bones after condensations were infected
with the RCAS-based viral constructs at E6. Bone and cartilage mineralized
structures were revealed with alizarin red (bone) and Alcian blue (cartilage)
histological stains. (G) Normal ossification pattern of the posterior
frontal bone in E15 embryos. The top, side and back of the skull are covered
with membranous bone. Infection with RCAS::noggin led to a loss of bone
mineralization in the posterior (H) parts of the frontal bone. By
contrast, infection of the posterior (I) and anterior (L)
frontal bone with RCAS::Bmp4 led to a loss of mineralized bone
material and its replacement with cartilage. (J) RCAS::Ihh
misexpression resulted in a significant decrease of frontal bone
mineralization, a phenotype that was similar to that of RCAS::PTHrP
misexpression (K). Scale bars: 0.7 cm in B,E; 2 mm in G.