Persistent retrograde labeling of adult rat retinal ganglion cells with the carbocyanine dye diI

To study the retrograde labeling of intact and axotomized retinal ganglion cells (RGCs) over long periods of time, we applied the carbocyanine dye diI to the superior colliculi (SC) and dorsal lateral geniculate nuclei (dLGN) in adult albino rats and examined the retinas by fluorescence microscopy after different periods of survival. Retrogradely labeled RGCs, which were observed in the retinas as early as 3 days after application of the dye, gradually increased in density so that by 7 days more than 80% of the RGCs were labeled and by 30 days diI-labeled cell densities were similar to those observed after short applications of other tracers. Using short-term retrograde labeling with fast blue (FB) as an independent marker of RGCs, it was determined that these neurons remained labeled with diI for periods of up to 9 months without apparent leakage of the tracer to other retinal cells. In addition, diI labeling persisted in the somata of more than 80% of axotomized RGCs whose contact with the source of label had been interrupted for 3 months. Thus, we propose that retrogradely transported diI is a useful label for quantitative studies of neuronal populations, even after axotomy.

[1]  S. Thanos,et al.  The use of rhodamine-B-isothiocyanate (RITC) as an anterograde and retrograde tracer in the adult rat visual system , 1987, Brain Research.

[2]  R. Linden,et al.  Postnatal changes in retinal ganglion cell and optic axon populations in the pigmented rat , 1983, The Journal of comparative neurology.

[3]  M. G. Honig,et al.  Fluorescent carbocyanine dyes allow living neurons of identified origin to be studied in long-term cultures , 1986, The Journal of cell biology.

[4]  M. Catsicas,et al.  Long-distance intraretinal connections in birds , 1987, Nature.

[5]  S. Thanos,et al.  A study in developing visual systems with a new method of staining neurones and their processes in fixed tissue. , 1987, Development.

[6]  C. Watt,et al.  A monoclonal antibody specific for retinal ganglion cells of mammals , 1985, Brain Research.

[7]  G. Bray,et al.  Influences of peripheral nerve grafts on the survival and regrowth of axotomized retinal ganglion cells in adult rats , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  J. Peyronnard,et al.  Differences in horseradish peroxidase labeling of sensory, motor and sympathetic neurons following chronic axotomy of the rat sural nerve , 1986, Brain Research.

[9]  U. Dräger,et al.  Thy-1 antigen: A ganglion cell specific marker in rodent retina , 1984, Neuroscience.

[10]  L. W. Swanson,et al.  A method for tracing biochemically defined pathways in the central nervous system using combined fluorescence retrograde transport and immunohistochemical techniques , 1981, Brain Research.

[11]  R. Linden,et al.  Massive retinotectal projection in rats , 1983, Brain Research.

[12]  T. Hökfelt,et al.  A method for specific transmitter identification of retrogradely labeled neurons: Immunofluorescence combined with fluorescence tracing , 1984, Brain Research Reviews.

[13]  S. Thanos,et al.  Major role for neuronal death during brain development: refinement of topographical connections. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[14]  C H Wang,et al.  Studies on the mechanism by which cyanine dyes measure membrane potential in red blood cells and phosphatidylcholine vesicles. , 1974, Biochemistry.

[15]  R. Mahley,et al.  Lipoprotein uptake by neuronal growth cones in vitro. , 1987, Science.

[16]  G. Raisman,et al.  Is Thy-1 expressed only by ganglion cells and their axons in the retina and optic nerve? , 1984, Journal of neurocytology.

[17]  J. Lavail,et al.  Retrograde Axonal Transport in the Central Nervous System , 1972, Science.

[18]  V. Perry Evidence for an amacrine cell system in the ganglion cell layer of the rat retina , 1981, Neuroscience.

[19]  J. Lund,et al.  Retrograde axonal transport of horseradish peroxidase by ganglion cells of the albino rat retina. , 1974, Brain research.

[20]  T. Jessell,et al.  Monoclonal antibodies against carbohydrate differentiation antigens identify subsets of primary sensory neurones , 1984, Nature.

[21]  N. Osborne,et al.  Localization of the Thy-1 antigen to the surfaces of rat retinal ganglion cells , 1982, Neurochemistry International.

[22]  S. Thanos,et al.  Axonal arborization in the developing chick retinotectal system , 1987, The Journal of comparative neurology.

[23]  S. Thanos,et al.  Axonal regeneration and synapse formation in the superior colliculus by retinal ganglion cells in the adult rat , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[24]  W. Catterall,et al.  Retrograde labeling, enrichment, and characterization of retinal ganglion cells from the neonatal rat , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  M. Murray,et al.  Viability of retinal ganglion cells after optic nerve crush in adult rats , 1984, Journal of neurocytology.