Fig. 1. Transfection of Ptc1
loop2 inhibits
neural cell proliferation and survival. HH11/12 stage chick embryos were
electroporated in ovo with a bi-cistronic vector containing
Ptc1
loop2 and GFP, or with the empty vector (pCIG-GFP) as
control, and assayed 12 and 24 hours post-electroporation (PE) for the
indicated markers. Transfected side of the neural tube is to the right side of
the figures. (A-D) 24 hours PE of Ptc1
loop2 caused
reduction of pH3-immunostaining on the transfected side, compared with the
control contralateral side (A). BrdU incorporation is reduced in GFP-positive
cells. Electroporated GFP-positive cells that have entered S phase of the cell
cycle are yellow (B). TUNEL staining (brown) is increased in
Ptc1
loop2 (C) and activated caspase 3-immunostaining is also
increased (D). (E-H) Ptc1
loop2 neural tubes 12 hours
PE show a reduction in pH3 immunostaining (E). BrdU incorporation is reduced
in GFP-positive cells (F). TUNEL (G) and caspase 3 immunostaining (H) are not
increased on the electroporated side 12 hours PE. (I-L) Control embryos
transfected with the empty vector (pCIG) identified by GFP (green) and
analyzed 12 hours PE, show an equal number of pH3-immunostaining cells on the
electroporated side compared with non-electroporated side (I), GFP-positive
cells can incorporate BrdU, as indicated by the elevated proportion of
double-labeled yellow cells (J). TUNEL staining (K) and activated caspase 3
immunostaining (L) are the same on transfected side and control contralateral
side. (M) Quantitative analysis of pH3-immunostained cells in
electroporated and non-electroporated sides of the neural tube. 12 hours PE
there was no significant changes in pH3 immunostaining; however, 24 hours PE,
the number of pH3 cells in Ptc1
loop2 EP embryos was
significantly reduced on the transfected side of the neural tube. Error bars
indicate s.d. (N) Quantitative analysis of
Ptc1
loop2-GFP/BrdU double labeled cells in ventral and
dorsal neural tubes, after a 4-hour BrdU pulse indicated a decrease of
15% in ventral regions and
50% in dorsal regions of the number of
cells incorporating BrdU by 12 hours PE, and a
60% decrease in ventral
regions and
40% decrease in dorsal regions by 24 hours PE. Error bars
indicate s.d. (O) Quantitative analysis of activated caspase 3-positive
cells in electroporated compared with non-electroporated side. 12 hours PE
there was no increase in caspase 3 immunostaining, while 24 hours PE there was
a
12 fold increase in caspase 3 immunostaining in neural tubes
transfected with Ptc1
loop2. Error bars indicate s.d. (M-O)
*P<0.05; **P<0.005;
***P<0.0001 control versus treated. (P) Summary
of the effect of Ptc1
loop2 on neuroepithelial cells.
(Q) Schematic representation of the Shh pathway.