Regenerative sprouting of retinal ganglion cells of adult hamsters induced by the epineurium of a peripheral nerve

Brain Research

Volumn 823, Issue 1-2, 1999, Pages 241-248

  Lai, M Y ^a   Cho, E Y P ^a  

^a CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

Hamster; Peripheral nerve; Regeneration; Retinal ganglion cell; Sprouting

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; FEMALE; IMPLANTATION; NERVE FIBER TRANSECTION; NERVE REGENERATION; NEWBORN; NONHUMAN; OPTIC NERVE; PERIPHERAL NERVE; PRIORITY JOURNAL; RETINA GANGLION CELL; SCHWANN CELL; SYRIAN HAMSTER; VITREOUS BODY;

ANIMALS; CRICETINAE; FEMALE; MESOCRICETUS; NERVE REGENERATION; PERIPHERAL NERVES; PERONEAL NERVE; RETINAL GANGLION CELLS; VITREOUS BODY; WOUNDS AND INJURIES;

EID: 0033608742     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(99)01202-0     Document Type: Article

References (37)

1. A. Acheson, P.A. Barker, R.F. Alderson, F.D. Miller, R.A. Murphy, Detection of brain-derived neurotrophic factor-like activity in fibroblasts and Schwann cells: inhibition by antibodies to NGF, Neuron 7 (1991) 265-275.
2. M. Bahr, R.P. Bunge, Functional status influences the ability of Schwann cells to support adult retinal ganglion cell survival and axonal regrowth, Exp. Neurol. 106 (1989) 27-40.
3. M. Bahr, G.W. Eschweiler, H. Wolburg, Precrushed sciatic nerve grafts enhance the survival and axonal regrowth of retinal ganglion cells in adult rats, Exp. Neurol. 116 (1992) 13-22.
4. R.R. Baichwal, J.W. Bigbee, G.H. DeVries, Macrophage-mediated myelin-related mitogenic factor for cultured Schwann cells, Proc. Natl. Acad. Sci. USA 85 (1988) 1701-1705.
5. L.I. Benowitz, A. Routtenberg, A membrane phosphoprotein associated with neural development, axonal regeneration, phospholipid metabolism, and synaptic plasticity, Trends Neurosci. 10 (1987) 527-532.
6. M. Berry, L. Rees, S. Hall, P. Yiu, J. Sievers, Optic axons regenerate into sciatic nerve isografts only in the presence of Schwann cells, Brain Res. Bull. 20 (1988) 223-231.
7. W. Beuche, R.L. Friede, The role of non-resident cells in Wallerian degeneration, J. Neurocytol. 13 (1984) 767-796.
8. E.Y.P. Cho, K.-F. So, Characterization of the sprouting response of axon-like processes from retinal ganglion cells after axotomy in adult hamsters: a model using intravitreal implantation of a peripheral nerve, J. Neurocytol. 21 (1992) 589-603.
9. E.Y.P. Cho, K.-F. So, Sprouting of axon-like processes from axotomized retinal ganglion cells is influenced by the distance of axotomy from the cell body and the mode of transplantation of the peripheral nerve, Restorative Neurol. Neurosci. 6 (1993) 29-34.
10. Q. Cui, K.-F. So, H.K. Yip, CNTF, but not other trophic factors, promotes axonal regeneration of distally axotomized retinal ganglion cells in adult hamsters, Proc. Aust. Neurosci. Soc. 9 (1998) 40.
11. S. David, C. Bouchard, O. Tsatas, N. Giftochristos, Macrophages can modify the non-permissive nature of the adult mammalian central nervous system, Neuron 5 (1990) 463-469.
12. B. Friedman, S.S. Scherer, J.S. Rudge, M. Helgren, D. Morrisey, J. McClain, D.Y. Wang, S.J. Wiegand, M.E. Furth, R.M. Lindsay, Regulation of ciliary neurotrophic factor expression in myelin-related Schwann cells in vivo, Neuron 9 (1992) 295-305.
13. H. Funakoshi, J. Frisen, G. Barbany, T. Timmusk, O. Zachrisson, V.M. Verge, H. Persson, Differential expression of mRNAs for neurotrophins and their receptors after axotomy of the sciatic nerve, J. Cell Biol. 123 (1993) 455-465.
14. H.A. Hansson, L.B. Dahlin, B. Lowenadler, G. Lundborg, S. Paleus, A. Skottner, Transient increase in insulin-like growth factor I immunoreactivity in rat peripheral nerves exposed to vibrations, Acta Physiol. Scand. 132 (1988) 35-41.
15. N.A. Hasan, M.M. Neumann, M.A. de Souky, K.-F. So, K.S. Bedi, The influence of predegenerated nerve grafts on axonal regeneration from prelesioned peripheral nerves, J. Anat. 189 (Pt 2) (1996) 293-302.
16. R. Heumann, S. Korsching, C. Bandtlow, H. Thoenen, Changes of Nerve Growth Factor synthesis in non-neuronal cells in response to sciatic nerve transection, J. Cell Biol. 104 (1987) 1623-1631.
17. R.D. Jacobson, I. Virag, J.H.P. Skene, A protein associated with axon growth, GAP-43, is widely distributed and developmentally regulated in rat CNS, J. Neurosci. 6 (1986) 1843-1855.
18. O. Lazarov-Spiegler, A.S. Solomon, M. Schwartz, Peripheral nerve-stimulated macrophages simulate a peripheral nerve-like regenerative response in rat transected optic nerve, Glia 24 (1998) 329-337.
19. O. Lazarov-Spiegler, A.S. Solomon, A.B. Zeev-Brann, D.L. Hirschberg, V. Lavie, M. Schwartz, Transplantation of activated macrophages overcomes central nervous system regrowth failure, FASEB J. 10 (1996) 1296-1302.
20. J. Leicester, J. Stone, Ganglion, amacrine and horizontal cells of the cat's retina, Vision Res. 7 (1967) 695-705.
21. Y. Li, G. Raisman, Schwann cells induce sprouting in motor and sensory axons in the adult rat spinal cord, J. Neurosci. 14 (1994) 4050-4063.
22. D. Lindholm, R. Heumann, M. Meyer, H. Thoenen, Interleukin-1 regulates synthesis of nerve growth factor in non-neuronal cells of rat sciatic nerve, Nature 330 (1987) 658-659.
23. X. Lu, P.M. Richardson, Inflammation near the nerve cell body enhances axonal regeneration, J. Neurosci. 11 (1991) 972-978.
24. L. Maffei, G. Carmignoto, V.H. Perry, P. Candeo, G. Ferrari, Schwann cells promote the survival of rat retinal ganglion cells after optic nerve section, Proc. Natl. Acad. Sci. USA 87 (1990) 1855-1859.
25. S. Mansour-Robaey, D.B. Clarke, Y.C. Wang, G.M. Bray, A.J. Aguayo, Effects of ocular injury and administration of brain-derived neurotrophic factor on survival and regrowth of axotomized retinal ganglion cells, Proc. Natl. Acad. Sci. USA 91 (1994) 1632-1636.
26. R. Martini, M. Schachner, Immunoelectron microscopic localization of neural cell adhesion molecules (L1, N-CAM and myelin-associated glycoprotein) in regenerating mouse sciatic nerve, J. Cell Biol. 106 (1988) 1735-1746.
27. M. Meyer, I. Matsuoka, C. Wetmore, L. Olson, H. Thoenen, Enhanced synthesis of brain-derived neurotrophic factor in the lesioned peripheral nerve: different mechanisms are responsible for the regulation of BDNF and NGF mRNA, J. Cell Biol. 119 (1992) 45-54.
28. C.N. Montero-Menei, A. Pouplard-Barthelaix, M. Gumpel, A. Baron-Van Evercooren, Pure Schwann cell suspension grafts promote regeneration of the lesioned septo-hippocampal cholinergic pathway, Brain Res. 570 (1992) 198-208.
29. R.K. Nath, S.E. Mackinnon, J.N. Jensen, W.C. Parks, Spatial pattern of type I collagen expression in injured peripheral nerve, J. Neurosurg. 86 (1997) 866-870.
30. T.F. Ng, K.-F. So, S.K. Chung, Influences of peripheral nerve grafts on the expression of GAP-43 in regenerating retinal ganglion cells in adult hamsters, J. Neurocytol. 24 (1995) 487-496.
31. M. Oudega, S. Varon, T. Hagg, Regeneration of adult rat sensory axons into intraspinal nerve grafts: promoting effects of conditioning lesion and graft predegeneration, Exp. Neurol. 129 (1994) 194-206.
32. P.M. Richardson, T. Ebendal, Nerve growth activities in rat peripheral nerve, Brain Res. 246 (1982) 57-64.
33. M. Sendtner, K.A. Stockli, H. Thoenen, Synthesis and localization of ciliary neurotrophic factor in the sciatic nerve of the adult rat after lesion and during regeneration, J. Cell Biol. 118 (1992) 139-148.
34. K.-F. So, A.J. Aguayo, Lengthy regrowth of cut axons from ganglion cells after peripheral nerve transplantation into the retina of adult rats, Brain Res. 328 (1985) 349-354.
35. H.S. Taskinen, M. Roytta, The dynamics of macrophage recruitment after nerve transection, Acta Neuropathol. (Berl) 93 (1997) 252-259.
36. P.K. Thomas, The connective tissue of peripheral nerve: an electron microscope study, J. Anat. 97 (1963) 35-44.
37. M. Vidal-Sanz, G.M. Bray, M.P. Villegas-Perez, S. Thanos, A.J. Aguayo, Axonal regeneration and synpase formation in the superior colliculus by retinal ganglion cells in the adult rat, J. Neurosci. 7 (1987) 2894-2909.