(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. 6. Expression of activated Notch1 results in overproduction of hindbrain
choroid plexus epithelium but not of other rhombic lip lineages.
(A) Schematic of a transverse section through the hindbrain (hb), with
the boxed area demarcating the region of the rhombic lip (RL) shown in B-D.
(B-D) Detection of Notch1, Gdf7 and Math1
mRNA on E11.5 hindbrain serial sections. Notch1 is expressed in the
rhombic lip, but not in the hindbrain roof plate epithelium (hRPe);
Gdf7 is expressed in the distal tip of the rhombic lip and into the
hRPe; and Math1 is expressed in the rhombic lip ventral to the
Gdf7 expression territory. (E-J,L) Comparison of singly
transgenic R26::stop-Notch1-ICD::IRES-nGFP (E,G,I) and doubly
transgenic Gdf7::cre; R26::stop-Notch1-ICD::IRES-nGFP (F,H,J,L)
brains. (E,F) Posterior (pos) whole-mount (wm) view of P7 brains processed for
Ttr mRNA detection [hindbrain choroid plexus epithelium (hCPe)
marker] showing enlarged hCPe in doubly transgenic tissue (F,H,J,L). (G,H)
Sagittal sections showing enlarged postnatal day 0 (P0) hCPe (red boxes) and
abnormal cerebellar architecture in doubly but not singly transgenic animals.
Inset in G shows Ttr+ hCPe on a serial section to that shown in G.
(I,J) Hematoxylin and Eosin staining at P7 shows abnormal cytoarchitecture of
hCP in doubly transgenic tissues. (K) P0 doubly transgenic
Wnt1::Flpe; Flpe-responsive nßgal indicator
distinguishing hCPe (green by immunodetection of ßgal) from underlying
mesenchyme and vasculature. BrdU was injected into animals at P0, and tissue
was harvested 2 hours later. BrdU immunodetection is shown in red. No
co-labeled cells were found in wild-type hCPe, as shown. (L) Similar BrdU
injection into doubly transgenic Gdf7::cre;
R26::stop-Notch1-ICD::IRES-nGFP animals showed numerous co-labeled cells
(arrowheads; GFP positivity identifying hCPe cells and expression of
Notch1-ICD, and red indicating BrdU incorporation as a measure of
proliferation). (M-V) Comparison of singly transgenic
R26::stop-Notch1-ICD::IRES-nGFP and doubly transgenic Math1::cre;
R26::stop-Notch1-ICD::IRES-nGFP brains. Coronal sections show no
differences in size, relative cell density (Barhl1 expression at P0)
or proliferation (Ki-67 immunodetection at P5 shown in red; U,V) of
Math1-derived rhombic lip lineages, including mossy fiber neurons of
the pontine gray nucleus (PGN, M-P), cerebellar granule cell precursors (CGC,
white arrowheads, Q-V) and granule cells of the cochlear nucleus (CNGC, red
arrowheads, Q,R). GFP positivity (immunodetection shown in green) reflects
expression of the Notch1-ICD transgene in PGN (O,P) and CGC (S,T).
White boxes in M-N demarcate regions of the PGN shown in O,P. DAPI is shown in
blue. 4v, fourth ventricle; bs, brainstem; cb, cerebellum; CP, choroid plexus;
hb, hindbrain; mz, post-mitotic mantle zone; RPe, roof plate epithelium; vz,
ventricular zone.