Characterization of dsRed2-positive cells in the doublecortin-dsRed2 transgenic adult rat retina

• Published in: Histochemistry and cell biology 2014-12, Vol.142 (6), p.601-617
• Main Authors: Trost, A., Schroedl, F., Marschallinger, J., Rivera, F. J., Bogner, B., Runge, C., Couillard-Despres, S., Aigner, L., Reitsamer, H. A.
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry; Biomedical and Life Sciences; Biomedicine; Cell Biology; Cellular biology; Developmental Biology; Doublecortin Domain Proteins; Doublecortin Protein; Female; Immunohistochemistry; Luminescent Proteins - genetics; Luminescent Proteins - metabolism; Male; Microtubule-Associated Proteins - genetics; Microtubule-Associated Proteins - metabolism; Neuropeptides - genetics; Neuropeptides - metabolism; Original Paper; Rats; Rats, Transgenic; Red Fluorescent Protein; Retina; Retina - cytology; Rodents; Transgenic animals
• ISSN: 0948-6143; 1432-119X
• DOI: 10.1007/s00418-014-1259-1

Doublecortin (DCX) is predominantly expressed in neuronal precursor cells and young immature neurons of the developing and adult brain, where it is involved in neuronal differentiation, migration and plasticity. Moreover, its expression pattern reflects neurogenesis, and transgenic DCX promoter-driven reporter models have been previously used to investigate adult neurogenesis. In this study, we characterize dsRed2 reporter protein-expressing cells in the adult retina of the transgenic DCX promoter-dsRed2 rat model, with the aim to identify cells with putative neurogenic activity. Additionally, we confirmed the expression of the dsRed2 protein in DCX-expressing cells in the adult hippocampal dentate gyrus. Adult DCX-dsRed2 rat retinas were analyzed by immunohistochemistry for expression of DCX, NF200, Brn3a, Sox2, NeuN, calbindin, calretinin, PKC-a, Otx2, ChAT, PSA-NCAM and the glial markers GFAP and CRALBP, followed by confocal laser-scanning microscopy. In addition, brain sections of transgenic rats were analyzed for dsRed2 expression and co-localization with DCX, NeuN, GFAP and Sox2 in the cortex and dentate gyrus. Endogenous DCX expression in the adult retina was confined to horizontal cells, and these cells co-expressed the DCX promoter-driven dsRed2 reporter protein. In addition, we encountered dsRed2 expression in various other cell types in the retina: retinal ganglion cells (RGCs), a subpopulation of amacrine cells, a minority of bipolar cells and in perivascular cells. Since also RGCs expressed dsRed2, the DCX-dsRed2 rat model might offer a useful tool to study RGCs in vivo under various conditions. Müller glial cells, which have previously been identified as cells with stem cell features and with neurogenic potential, did express neither endogenous DCX nor the dsRed2 reporter. However, and surprisingly, we identified a perivascular glial cell type expressing the dsRed2 reporter, enmeshed with the glia/stem cell marker GFAP and colocalizing with the neural stem cell marker Sox2. These findings suggest the so far undiscovered existence of perivascular associated cell with neural stem cell-like properties in the adult retina.