Regenerative and other responses to injury in the retinal stump of the optic nerve in adult albino rats: transection of the intraorbital optic nerve.

The proximal stump of the optic nerve was examined by electron microscopy from 1 d to 8 wk (dpo/wpo) after intraorbital transection. At 1 dpo a layer of axonal, cytoplasmic and myelin debris approximately 15 microns thick was present at the cut end. A zone approximately 25 microns thick of abnormal and partly degenerate tissue composed of many swollen axons filled with organelles of predominantly abnormal appearance lay between the zone of debris and more proximal levels of the optic nerve, which retained a normal appearance. The earliest putative axonal sprouts were seen at 1 dpo in this zone. By 2 dpo, bundles of small nonmyelinated axons containing microtubules, almost certainly axonal sprouts, had grown out from more proximal regions of the proximal stump and extended as far as its cut end. By 3 dpo, large numbers of axonal sprouts, as well as large numbers of macrophages and newly formed blood vessels, were seen close to the cut end of the proximal stump. Glial cells were not seen to accompany these early outgrowing bundles of axonal sprouts. By 5 dpo, the number of sprouts and macrophages had increased; many bundles of sprouts were now in contact with the surface of astrocytes, which were partly covered by basal lamina. At 7 dpo most of the macrophages had disappeared from the most distal part of proximal stump and bundles of axonal sprouts, associated with astrocytes, which in some cases had penetrated and were fasciculating such bundles, were present at the cut end. The regenerating axonal sprouts in the scar-like tissue at the distal end of the proximal stump of the optic nerve declined in numbers sharply at 2 wpo and only a few sprout-like axonal profiles were present by 8 wpo. Thus while ultimately abortive the early regenerative response is vigorous and involves the outgrowth of a large number of axonal sprouts in the first week after injury.

[1]  A. Aguayo,et al.  Marked increase in beta-tubulin mRNA expression during regeneration of axotomized retinal ganglion cells in adult mammals , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[2]  A. Aguayo,et al.  Temporal changes in beta-tubulin and neurofilament mRNA levels after transection of adult rat retinal ganglion cell axons in the optic nerve , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[3]  A. Aguayo,et al.  Rapid and protracted phases of retinal ganglion cell loss follow axotomy in the optic nerve of adult rats. , 1993, Journal of neurobiology.

[4]  A. Lieberman,et al.  Regeneration of adult rat CNS axons into peripheral nerve autografts: ultrastructural studies of the early stages of axonal sprouting and regenerative axonal growth , 1992, Journal of neurocytology.

[5]  J. Silver,et al.  Reduction of neurite outgrowth in a model of glial scarring following CNS injury is correlated with the expression of inhibitory molecules on reactive astrocytes , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[6]  A. Lozano,et al.  Expression of the growth-associated protein GAP-43 in adult rat retinal ganglion cells following axon injury , 1991, Neuron.

[7]  J. Silver,et al.  Inhibition of neurite outgrowth on astroglial scars in vitro , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  S. David,et al.  Macrophages can modify the nonpermissive nature of the adult mammalian central nervous system , 1990, Neuron.

[9]  F. J. Liuzzi,et al.  Proteolysis is a critical step in the physiological stop pathway: mechanisms involved in the blockade of axonal regeneration by mammalian astrocytes , 1990, Brain Research.

[10]  M. Schwab,et al.  Axonal regeneration in the rat spinal cord produced by an antibody against myelin-associated neurite growth inhibitors , 1990, Nature.

[11]  D Giulian,et al.  The role of mononuclear phagocytes in wound healing after traumatic injury to adult mammalian brain , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  C. Fernández Viadero,et al.  The microvascular system of the optic nerve in control and enucleated rats. , 1989, Microvascular research.

[13]  H. Kanaya,et al.  Regeneration in the rat optic nerve after cold injury. , 1989, Journal of neurosurgery.

[14]  M. Berry,et al.  Electron microscopic study of the interaction of axons and glia at the site of anastomosis between the optic nerve and cellular or acellular sciatic nerve grafts , 1989, Journal of neurocytology.

[15]  M. Berry,et al.  Regeneration of axons from the adult rat optic nerve: Influence of fetal brain grafts, laminin, and artificial basement membrane , 1989, The Journal of comparative neurology.

[16]  M. Berry,et al.  Fetal brain grafts rescue adult retinal ganglion cells from axotomy‐induced cell death , 1989, The Journal of comparative neurology.

[17]  N. Vesselkin,et al.  A preliminary description of the regeneration of optic nerve fibers in a reptile, Vipera aspis , 1989, Brain Research.

[18]  A. Harvey,et al.  Ultrastructural and immunohistochemical analysis of axonal regrowth and myelination in membranes which form over lesion sites in the rat visual system , 1988, Journal of neurocytology.

[19]  M. Berry,et al.  Response of axons and glia at the site of anastomosis between the optic nerve and cellular or acellular sciatic nerve grafts , 1988, Journal of neurocytology.

[20]  W. Gispen,et al.  Changes in the distribution of the neuron-specific B-50, neurofilament protein and glial fibrillary acidic proteins following an unilateral mesencephalic lesion in the rat , 1988, Brain Research Bulletin.

[21]  M. Schwab,et al.  Oligodendrocytes and CNS myelin are nonpermissive substrates for neurite growth and fibroblast spreading in vitro , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[22]  M. Fishman,et al.  Cloning of human GAP 43: Growth association and ischemic resurgence , 1988, Neuron.

[23]  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.

[24]  M. Berry,et al.  The Role of Basal Lamina in Axon Regeneration , 1988 .

[25]  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.

[26]  R. Lasek,et al.  Astrocytes block axonal regeneration in mammals by activating the physiological stop pathway. , 1987, Science.

[27]  V. Perry,et al.  The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration , 1987, The Journal of experimental medicine.

[28]  G. Stoll,et al.  Macrophages in the peripheral nervous system and astroglia in the central nervous system of rat commonly express apolipoprotein E during development but differ in their response to injury , 1986, Neuroscience Letters.

[29]  K. Barron,et al.  Qualitative and quantitative ultrastructural observations on retinal ganglion cell layer of rat after intraorbital optic nerve crush , 1986, Journal of neurocytology.

[30]  K. Bedi,et al.  A quantitative morphological study of interstrain variation in the developing rat optic nerve , 1986, The Journal of comparative neurology.

[31]  M. Berry,et al.  Unequivocal Regeneration of Rat Optic Nerve Axons into Sciatic Nerve Isografts , 1986 .

[32]  J. Kiernan Axonal and vascular changes following injury to the rat's optic nerve. , 1985, Journal of anatomy.

[33]  K. So,et al.  Lengthy regrowth of cut axons from ganglion cells after peripheral nerve transplantation into the retina of adult rats , 1985, Brain Research.

[34]  G. Raisman Specialized neuroglial arrangement may explain the capacity of vomeronasal axons to reinnervate central neurons , 1985, Neuroscience.

[35]  I. Mcquarrie Effect of a conditioning lesion on axonal sprout formation at nodes of ranvier , 1985, The Journal of comparative neurology.

[36]  R. Sidman,et al.  Retinal ganglion cells and axons survive optic nerve transection. , 1984, The International journal of neuroscience.

[37]  P. Reier,et al.  Astrocytic membrane morphology: Differences between mammalian and amphibian astrocytes after axotomy , 1984, The Journal of comparative neurology.

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

[39]  P. Richardson,et al.  Regeneration and retrograde degeneration of axons in the rat optic nerve , 1982, Journal of neurocytology.

[40]  M. Berry,et al.  Regeneration of ganglion cell axons in the adult mouse retina , 1982, Brain Research.

[41]  J. Skene,et al.  Axonally transported proteins associated with axon growth in rabbit central and peripheral nervous systems , 1981, The Journal of cell biology.

[42]  B. Grafstein,et al.  Early stages of axonal regeneration in the goldfish optic tract: An electron microscopic study , 1980, Journal of neurocytology.

[43]  D Bray,et al.  Movement and extension of isolated growth cones. , 1977, Experimental cell research.

[44]  M. Singer,et al.  The ultrastructure of regeneration in the severed newt optic nerve. , 1974, The Journal of experimental zoology.

[45]  P. Reier,et al.  Regeneration and remyelination ofXenopus tadpole optic nerve fibres following transection or crush , 1974, Journal of neurocytology.

[46]  M. Carpenter The Fine Structure of the Nervous System , 1970, Neurology.

[47]  A. Peters,et al.  Nerve Fibres in Optic Nerve of Rat , 1967, Nature.

[48]  J. E. Vaughn,et al.  MICROTUBULES AND FILAMENTS IN THE AXONS AND ASTROCYTES OF EARLY POSTNATAL RAT OPTIC NERVES , 1967, The Journal of cell biology.

[49]  D. D.-B.,et al.  Degeneration and Regeneration of the Nervous System , 1930, Nature.