Influences of peripheral nerve grafts on the survival and regrowth of axotomized retinal ganglion cells in adult rats
Open Access
- 1 January 1988
- journal article
- research article
- Published by Society for Neuroscience in Journal of Neuroscience
- Vol. 8 (1) , 265-280
- https://doi.org/10.1523/jneurosci.08-01-00265.1988
Abstract
To investigate the role of extrinsic influences on the survival and growth of axotomized retinal ganglion cells (RGCs) in the mature mammalian CNS, both optic nerves (ONs) of adult rats were transected intraorbitally and, on one side, replaced by an autologous segment of peripheral nerve (PN) that had been left unconnected distally. The survival of RGCs and the regrowth of their cut axons into the PN grafts were assessed using morphometric techniques, neuroanatomic tracers, and immunologic cell markers to identify and count RGCs at times ranging from 15 d to 9 months. It was observed that (1) in the absence of a PN graft, more than 90% of the RGCs died by 1 month after axotomy; (2) between 1 and 3 months after axotomy, survival of RGCs in the PN- grafted retinas was enhanced 2–4-fold; (3) nearly 20% of the surviving RGCs regrew lengthy axons into the grafts; and (4) although the density of surviving RGCs in PN-grafted retinas decreased significantly between 1 and 3 months after axotomy, the densities of RGCs with axons extending into the graft remained relatively stable. These results confirm that in the adult rat retina, neuronal death is a major effect of axotomy near the cell soma. Although such lesions lead to the degeneration of many RGCs, we show that extrinsic influences introduced by the apposition of a PN segment at the time of severing the ON can rescue a substantial number of these neurons. Because the enhanced survival of many axotomized RGCs in the PN-grafted retinas appears to be limited to the first few weeks after injury, while those of RGCs that regenerate axons into the grafts do not show a parallel decline, it is possible that, in these experiments, neuronal viability depends on a spectrum of differently timed influences that may include the early diffusion of critical molecules arising from the graft and the subsequent establishment of more complex interactions with graft components.This publication has 45 references indexed in Scilit:
- Evidence for an amacrine cell system in the ganglion cell layer of the rat retinaNeuroscience, 1981
- Changes in axonally transported proteins during axon regeneration in toad retinal ganglion cells.The Journal of cell biology, 1981
- Axon reaction in dorsal motor vagal and hypoglossal neurons of the adult rat. light microscopy and RNA‐cytochemistryJournal of Comparative Neurology, 1980
- Avian retinal ganglion cells resistant to degeneration after optic nerve lesionExperimental Neurology, 1980
- The projection of the temporal retina in rats, studied by retrograde transport of horseradish peroxidaseExperimental Brain Research, 1979
- EFFECTS OF NERVE GROWTH-FACTOR AND ITS ANTISERUM ON SYNAPSES IN SUPERIOR CERVICAL GANGLION OF GUINEA-PIG1978
- A three-group classification of rat retinal ganglion cells: histological and physiological studiesBrain Research, 1977
- Morphometric analysis of rat superior cervical ganglion after axotomy and nerve growth factor treatmentJournal of Neurocytology, 1976
- A quantitative analysis of the distribution of ganglion cells in the cat's retinaJournal of Comparative Neurology, 1965
- DEGENERATION OF GANGLION CELL FOLLOWING AXONAL INJURYArchives of Ophthalmology (1950), 1933