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Fig. 4. Defects in laminar structure and cell specification in Ptf1a
mutant retinas. (A-F) X-gal staining of retinal sections from E18.5
Ptf1aCre/+;R26R embryos (A) and
Ptf1aCre/Cre;R26R embryos (B) counterstained with Fast
Red. (C,E) Higher-magnification images of the areas in the solid and broken
rectangles in A, respectively. (D,F) Higher-magnification images of the areas
in the solid and broken rectangles in B, respectively. Arrows in E indicate
representative developing horizontal cells and the bracket in E indicates
normal location of maturing amacrine cells in the E18.5 retina. The bracket in
F indicates lacZ-positive nerve fiber layer, which is thicker than
the control lacZ-negative nerve fiber layer (indicated by the small
bracket in E). (G-J) Hematoxylin and Eosinstained sections of wild-type
and mutant retinas at E18.5. Higher-magnification pictures of G and H are
shown in I and J, respectively. Arrowheads in H indicate a front-line of cells
in the outer neuroblastic layer invading into the GCL. (K,L)
Wild type and Ptf1aCre/Cre E18.5 retinal sections were
immunostained with an anti-Brn3b antibody. Scale bars: in B, 100 µm for
A,B; in H, 50 µm for E-H; in D, 25 µm for C,D; in L, 25 µm for K,L;
in J, 10 µm for I,J. (M) Top, increased ganglion cell number in
Ptf1aCre/Cre retinas. Bottom, no significant change in
central retinal thickness in the mutant. Histograms represent the
mean±s.d. of measurements from five animals of each genotype.
*P<0.001. Abbreviations: GCL, ganglion cell layer; IPL,
inner plexiform layer.