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Resolution: standard / high Figure 7.
Distribution of Zic proteins in mouse meningeal membrane. Mouse sections were derived from coronal sections through the forebrain at embryonic
day 12.5, E12.5 (A, E), embryonic day 14.5, E14.5 (B, C, F, G) or 12 weeks after birth,
P12w (D, H). Images (A, E), (B, F) and (C, G) indicate the same regions respectively.
Image in (H) is a higher magnification of the boxed region in (D). Immunostaining
with CXY2 (A, B, D, H), CXY2/vimentin (E, F), and CXY2/CS56 (C), and differential
interference contrast image (G) are shown. Zic signals are indicated by red in (A--C,
E, F), and brown in (D, H). The colour green indicates CS56 (C) and vimentin (E, F)
immunoreactivities. In (C), the ZIC-like and CS56 immunoreactivities overlapped within
the arachnoid layer that expresses vimentin; whereas, only CS56--positive signals
were detected within the chondrogenic area, between the two broken lines. The white
line indicates the interface between meningeal tissue and cerebral cortex. CS56--positive
signals were detected in the region that forms the basal lamina (asterisks). In the
adult mouse brain, Zic proteins were still produced in the meningeal cells, as well
as the lateral septal nucleus, medial septal nucleus, and diagonal band (D). The positive
signals were detected in the arachnoid and perivascular cells (H). a, arachnoid layer;
ch, chondrogenic region (prospective temporal bone); ctx, cerebral cortex; db, diagonal
band; ls, lateral septal nucleus; ms, medial septal nucleus; v, vessel. Thick scale
bar, 1 mm; thin scale bar, 100 μm.
Aruga et al. BMC Cancer 2010 10:79 doi:10.1186/1471-2407-10-79 |