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Figure 3 | Molecular Brain

Figure 3

From: The transcription factor RBP-J is essential for retinal cell differentiation and lamination

Figure 3

Alteration of cell types in mature RBP-J deficient retinae. Immunostaining (green) and in situ hybridization performed on P21 sections from Chx10Cre-RBPf/fand wild-type retinae. (A-H) Compared to control retinae, both rhodopsin+ and Gnat1+ rod photoreceptor cells, and PNA+ and Arr3+ cone photoreceptor cells are significantly increased in RBP-J deficient retinae. (I-L) Brn3+ and Nefl+ ganglion cells are greatly decreased in RBP-J deficient retinae compared to wild-type. (M-T) Interneurons, including NF165+ horizontal cells (M, N), syntaxin+ amacrine cells (O, P), PKCα+ rod bipolar cells (Q, R), and NK3+ cone bipolar cells (S, T) are all decreased in RBP-J deficient retinae, relative to wild-type controls. (U-Z) Numbers of glutamine synthetase (GS)+ and clusterin+ Müller glial cells in Chx10Cre-RBPf/fretinae are comparable to those in wild-type retinae, although GFAP+ endfeet of Müller glial cells are increased in the deficient retina. (A') Comparison of percentages of Rhodopsin+, PNA+, Brn3+, NF165+, syntaxin+, PKCα+, NK3+ and GS+ cells in the total population of retinal cells between Chx10Cre-RBPf/fand wild-type retinae (*P < 0.05, **P < 0.01). GCL, ganglion cell layer; INL, inner nuclear layer; IPL, inner plexiform layer; ONL, outer nuclear layer; OPL, outer plexiform layer. Hoechst counterstaining is shown in magenta. Scale bar, 100 μm.

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