1986
DOI: 10.1679/aohc.49.69
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Nerve regeneration through allogenic nerve grafts in mice.

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Cited by 30 publications
(25 citation statements)
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“…The evidence in the present study indicates that an almost identical process of nerve regeneration occurs in the cryo-treared xenogeneic graft as in similarly treated autografts (IDE, 1983 ;ICE et al, 1983) and allografts (OSAWA et al, 1986). In short, Schwann cells in the graft are degraded, whereas their basal laminae remain in the form of tubes without being phagocytized by macrophages, and regenerating axons grow out through such basal lamina tubes.…”
Section: Discussionsupporting
confidence: 61%
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“…The evidence in the present study indicates that an almost identical process of nerve regeneration occurs in the cryo-treared xenogeneic graft as in similarly treated autografts (IDE, 1983 ;ICE et al, 1983) and allografts (OSAWA et al, 1986). In short, Schwann cells in the graft are degraded, whereas their basal laminae remain in the form of tubes without being phagocytized by macrophages, and regenerating axons grow out through such basal lamina tubes.…”
Section: Discussionsupporting
confidence: 61%
“…It has been recognized that these treatments improve to some extent the nerve regeneration in allogeneic grafts. In a previous study using sciatic nerve grafts between two different strains of mice, C57BL/6N and C3H/HeN, we demonstrated that Schwann cell basal lamina tubes serve as effective conduits for regenerating nerves even in the allograft (OSAWA et al, 1986). Judging from the fact that basal laminae and collagen fibrils were not phagocytized by macrophages, but left apparently intact in the allogeneic grafts, it can be assumed that there were no significant differences in the components of these extracellular substances in the above two strains of mice, and that little or no immunological reaction to those substances occurred between these strains.…”
Section: Discussionmentioning
confidence: 87%
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“…To overcome this difficulty, we attempt to perform frozen allogeneic nerve grafts [5] in dogs. No immunosuppressive reagents are required with this method, and successful axonal regeneration and myelination has been confirmed by electron microscopy in mice [13], rats [14], rabbits [20], dogs [6] and monkeys [19]. Given this morphological evidence, reasonable functional recovery appears likely.…”
mentioning
confidence: 80%