Semi-automated, quantitative analysis of retinal ganglion cell morphology in mice selectively expressing yellow fluorescent protein

• Published in: Experimental eye research 2012-03, Vol.96 (1), p.107-115
• Main Authors: Oglesby, Ericka, Quigley, Harry A., Zack, Donald J., Cone, Frances E., Steinhart, Matthew R., Tian, Jing, Pease, Mary E., Kalesnykas, Giedrius
• Format: Article
• Language: English
• Subjects: Animal models; Animals; Bacterial Proteins - metabolism; Brightness; Cell Count; Cell Line; Computer programs; Confocal microscopy; Cytology; Data processing; Eye; Fluorescent Dyes - metabolism; ganglion cell; glaucoma; Injuries; Luminescent Proteins - metabolism; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microscopy, Confocal; Microscopy, Fluorescence; mouse; Neurons; neuropathy; optic nerve; Promoter Regions, Genetic; Promoters; Retina; Retinal ganglion cells; Retinal Ganglion Cells - cytology; Retinal Ganglion Cells - metabolism; software; Thy-1 Antigens; Transgenic mice; yellow fluorescent protein
• ISSN: 0014-4835; 1096-0007
• DOI: 10.1016/j.exer.2011.12.013

The development of transgenic mouse lines that selectively label a subset of neurons provides unique opportunities to study detailed neuronal morphology and morphological changes under experimental conditions. In the present study, a mouse line in which a small number of retinal ganglion cells (RGCs) express yellow fluorescent protein (YFP) under control of the Thy-1 promoter was used (Feng et al., 2000). We characterized the number, distribution by retinal region and eccentricity of YFP-labeled RGCs using fluorescence microscopy and Stereo Investigator software (MicroBrightField, VT, USA). Then, we captured images of 4–6 YFP-expressing RGCs from each of 8 retinal regions by confocal microscopy, producing 3-dimensional and flattened data sets. A new semi-automated method to quantify the soma size, dendritic length and dendritic arbor complexity was developed using MetaMorph software (Molecular Devices, PA, USA). Our results show that YFP is expressed in 0.2% of all RGCs. Expression of YFP was not significantly different in central versus peripheral retina, but there were higher number of YFP-expressing RGCs in the temporal quadrant than in the nasal. By confocal-based analysis, 58% of RGCs expressing YFP did so at a high level, with the remainder distributed in decreasing levels of brightness. Variability in detailed morphometric parameters was as great between two fellow retinas as in retinas from different mice. The analytic methods developed for this selective YFP-expressing RGC model permit quantitative comparisons of parameters relevant to neuronal injury. ► YFP-expressing retinal ganglion cells were studied. ► A semi-automated method was used to analyze the morphology of these cells. ► Quantitative measures of morphometric parameters were obtained. ► This method can benefit in studies of cell changes in eye disease models.