PLoS ONE · 2014 · 96 citations · 58 references
Retinal TherapiesPeripheral NervesOptic NerveCellular PhysiologyGanglion CellRetinaGanglion Cell DeathStem CellsHealth SciencesAxonal InjuryOphthalmologyMelanopsin Ganglion CellsRat RetinaNervous SystemCell BiologyOcular TissueMicrosurgical Nerve RepairPhotoreceptor CellExperimental OphthalmologyCellular NeuroscienceOptic Nerve TransectionNeuroscienceGlaucomaMedicineRetinal Biology
We report that the most common retinal ganglion cell type that remains after optic nerve transection is the M1 melanopsin ganglion cell. M1 ganglion cells are members of the intrinsically photosensitive retinal ganglion cell population that mediates non-image-forming vision, comprising ∼2.5% of all ganglion cells in the rat retina. In the present study, M1 ganglion cells comprised 1.7±1%, 28±14%, 55±13% and 82±8% of the surviving ganglion cells 7, 14, 21 and 60 days after optic nerve transection, respectively. Average M1 ganglion cell somal diameter and overall morphological appearance remained unchanged in non-injured and injured retinas, suggesting a lack of injury-induced degeneration. Average M1 dendritic field size increased at 7 and 60 days following optic nerve transection, while average dendritic field size remained similar in non-injured retinas and in retinas at 14 and 21 days after optic nerve transection. These findings demonstrate that M1 ganglion cells are more resistant to injury than other ganglion cell types following optic nerve injury, and provide an opportunity to develop pharmacological or genetic therapeutic approaches to mitigate ganglion cell death and save vision following optic nerve injury.
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