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Fig. 10. Increased abundance of neuroepithelium-derived cells in the E11.5
Cx43-PCKO embryo. (A) Wild-type E11.5 expression pattern of
P3pro-Cre+:Cx43+/+, EYFP-labeled cells (green signal)
are limited to the neural tube, dorsal root ganglia (drg), peripheral nerves
(pn), sympathetic ganglia (sg) and small circumscribed collections of labeled
cells flanking the trachea (t) and esophagus. Sections in A-F are
counterstained with propidium iodide to highlight the nuclei; overlap with
EYFP appears as yellow signal. (B) Labeled cells flanking the trachea
are shown migrating into the OFT of a control E11.5 embryo. (C) Section
from an E11.5 Cx43-PCKO EYFP embryo at the level of the heart, showing an
increased abundance of labeled cells outside of the neural tube in comparison
with the control littermate. (D) Labeled cells are abundant in and
around the tracheal region adjacent to the OFT in the Cx43-PCKO embryo at
E11.5. (E,F) Labeled cells in sections from E11.5
Wnt1-Cre+ control (E) and Cx43-WCKO embryos (F) at the level of the
heart share a similar distribution to that of P3pro-Cre+ controls,
except in the neural tube where the Wnt1-Cre+ cells have a more
limited distribution. (G) Radioactive in situ hybridization of E11.5
control embryos shows plexin A2 mRNA (pink) distributed in the neural tube
(arrowhead) and in the OFT (arrow), as well as in paratracheal tissue adjacent
to the OFT. (H) In contrast to the control embryos, Cx43-PCKO embryos
express higher levels of plexin A2 (pink) in the neural tube (arrowhead), OFT
(arrow) and paratracheal tissue, as well as elsewhere in the embryo.
(I,J) Immunostaining for the presence of Pax3 (red) in control
(I) and Cx43-PCKO (J) sections (indicated by arrows) at E11.5 reveals an
unchanged expression pattern in the mutant embryos. (K) Cre recombinase
expression (green) is absent in control embryos. (L) Cre expression is
seen primarily at the dorsal aspect of the neural tube in Cx43-PCKO embryos at
this stage (arrows). Arrowheads indicate the ventral boundary of the neural
tube. Scale bar: 200 µm for A-F; 100 µm for G,H; 400 µm for I-L.