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An immunocytochemical marker for hamster retinal ganglion cells
Authors:P. G. Bhide   W. C. West   K. R. Fry  D. O. Frost
Affiliation:(1) Department of Neurology, Massachusetts General Hospital and Program in Neuroscience, Harvard Medical School, 02114 Boston, MA, USA;(2) Department of Psychology, Tufts University, 02155 Medford, MA, USA;(3) Alice R. McPherson Laboratory of Retina Research, The Center for Biotechnology, Baylor College of Medicine, 77381 The Woodlands, TX, USA;(4) Department of Pharmacology and Experimental Therapeutics, University of Maryland School of Medicine, 21201 Baltimore, MD, USA;(5) Developmental Laboratory, Massachusetts General Hospital East, 149 13th Street, 02129 Charlestown, MA, USA
Abstract:Summary We examined the specificity and developmental time course of the labelling of retinal ganglion cells in Syrian hamsters by a monoclonal antibody AB5. In adult hamsters, AB5 selectively labelled somata in the ganglion cell layer, dendrites in the inner plexiform layer and axons in the nerve fibre layer. When retinal ganglion cells were retrogradely labelled with Dil prior to AB5 immunocytochemistry, all of the retrogradely labelled retinal ganglion cells in the ganglion cell layer were AB5 immunoreactive, indicating that AB5 labels all classes of ganglion cell in that layer. In retinae depleted of retinal ganglion cells by neonatal optic nerve transections, AB5 did not label any somata or processes, indicating that AB5 specifically labels retinal ganglion cells. During development, AB5 labelling first appeared as a weak staining of cell bodies in the ganglion cell layer on postnatal day 12 (P12; PO=first 24 h following birth) and acquired the staining pattern seen in the adult by postnatal day 14. From the onset of AB5 immunoreactivity, AB5-labelled somata of varying sizes were present across the entire retinal surface. Although AB5 labelled retinal ganglion cell axons in the nerve fibre layer of the retina it did not label the optic nerve or retinal ganglion cell axons in the brain at any age examined. AB5 labelling was also found to be compatible with bromodeoxyuridine immunocytochemistry and, therefore, useful for determining the time of generation of hamster retinal ganglion cells.
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