A Battery of Cell- and Structure-specific Markers for the Adult Porcine Retina

被引:48
作者
Johansson, Ulrica Englund [1 ]
Eftekhari, Sajedeh [1 ]
Warfvinge, Karin [1 ]
机构
[1] Lund Univ, Div Ophthalmol, Dept Clin Sci, S-22184 Lund, Sweden
基金
瑞典研究理事会;
关键词
pig retina; photoreceptors; rods; cones; horizontal cells; bipolar cells; amacrine cells; ganglion cells; retinal pigment epithelium; Muller cells; FULL-THICKNESS RETINA; PIGMENT EPITHELIAL-CELLS; P347L TRANSGENIC PIGS; LARGE ANIMAL-MODEL; PROTEIN-KINASE-C; IMMUNOHISTOCHEMICAL LOCALIZATION; MULTIFOCAL ELECTRORETINOGRAM; SUBRETINAL SPACE; PROGENITOR CELLS; GANGLION-CELLS;
D O I
10.1369/jhc.2009.954933
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The pig is becoming an increasingly used non-primate model in experimental studies of human retinal diseases and disorders. The anatomy, size, and vasculature of the porcine eye and retina closely resemble their human counterparts, which allows for application of standard instrumentation and diagnostics used in the clinic. Despite many reports that demonstrate immunohistochemistry as a useful method for exploring neuropathological changes in the mammalian central nervous system, including the pig, the porcine retina has been sparsely described. Hence, to facilitate further immunohistochemical analysis of the porcine retina, we report on the successful use of a battery of antibodies for staining of paraformaldehyde-fixed cryosectioned retina. The following antibodies were evaluated for neuronal cells and structures: recoverin (cones and rods), Rho4D2 (rods), transducin-gamma (cones), ROM-1 (photoreceptor outer segments), calbindin (horizontal cells), PKC-alpha (bipolar cells), parvalbumin (amacrine and displaced amacrine cells), and NeuN (ganglion cells and displaced amacrines). For detecting synaptic connections in fiber layers, we used an antibody against synaptobrevin. For detecting retinal pigment epithelium, we studied antibodies against cytokeratin and RPE65, respectively. The glial cell markers used were bFGF (Muller cells and displaced amacrine cells), GFAP (Muller cells and astrocytes), and vimentin (Muller cells). Each staining effect was evaluated with regard to its specificity, sensitivity, and reproducibility in the identification of individual cells, specific cell structures, and fiber layers, respectively. The markers parvalbumin and ROM-1 were tested here for the first time for the porcine retina. All antibodies tested resulted in specific staining of high quality. In conclusion, all immunohistochemical protocols presented here will be applicable in fixed, cryosectioned pig retina. (J Histochem Cytochem 58:377-389, 2010)
引用
收藏
页码:377 / 389
页数:13
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