Figure 1 of Vieira, Mol Vis 2008; 14:2390-2403.


Figure 1. Dlg1 mRNA distribution in the control retina and protein localizations in the adult retina and during development from control and Trp1/Tag mice using immunohistochemistry. A and B show Dlg1 mRNA localization whereas C-K show the Dlg1 protein distribution in the adult mouse retina from the control mouse (C and D) and from the Trp1/Tag mouse model (E-K) at P15 (E), P20 and P25 (F-H), P30, and three months (I-K). A and C show the negative controls for B and D, respectively. Dlg1 mRNA and protein distributions were widely expressed in the ganglion cell layer (GCL), the inner nuclear layer (INL), the outer nuclar layer (ONL), and the photoreceptor inner segments (IS) of the control mouse retina. Very strong staining was detected in the outer plexiform layer (OPL) and the external limiting membrane (elm). However, faint staining of Dlg1 mRNA was found in the inner plexiform layer whereas its protein was strongly detected. Futhermore, in the inner nuclear layer, Dlg1 labeling was stronger at either side of the layer than in its center (indicated by an asterisk; D). Retina from the transgenic Trp1/Tag mouse model of ocular tumor continued to express Dlg1 protein (E-K). However, changes in the distribution of Dlg1 protein was observed from P20. In the central region adjacent to the mass of tumoral cells, Dlg1 immunolabeling in photoreceptor segments (IS) seemed to be reduced (F,G,I). A lower intensity of Dlg1 immunolabeling was shown in the OPL compared to the control retina (F,G,I). We also observed that immunolabeling in the INL appeared to be more diffuse in transgenics than in controls, possibly reflecting more labeling at the cortical regions than at membranous regions (F,I). In addition, from P30, the RPE and choroid (Ch) no longer stained positive for Dlg1 protein (J) in the posterior pole. The tumor cells (TC) had very faint staining for Dlg1 protein at these stages (H,K).