Yan ke xue bao = Eye science · 1998
Peripheral nerve and transgene cells transplantation in the treatment of experimental neuropathy of SD rats.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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История · было → стало
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Ge J, Li Y, Zhuo Y, Guo Y
Аннотация
PURPOSE: To observe whether optic nerve can regenerate by peripheral nerve transplantation and GDNF gene transfer.
METHODS: Optic nerve was transected about 2 mm posterior to the eye to establish experimental models of optic neuropathy. Sciatic nerve was sutured to the sheath of injury optic nerve by a 10-0 nylon, pcDNA3-GDNF was smeared to the joint and injected to the vitreous cavity. The regenerated retinal ganglion cells axons were observed by HRP. The retina and optic nerve were observed by pathohistological methods.
RESULTS: Some retinal ganglion cells with regenerated axons could be seen a week after transplantation with large cell bodies. The cells could be identified by HRP. The regenerated nerve fibers grew to the transplanted sciatic nerve. Then the number of retinal ganglion cells with regenerated axons increased with time going. Only a few regenerated retinal ganglion cells could be seen two months after transplantation. The large retinal ganglion cells were seen to have plenty of cytoplasms and be in an active state under electron microscope. Some nerve fibers could be seen in the joint. Sciatic nerve transplantation combined with GDNF gene therapy could increase the amount of retinal ganglion cells with regenerated axons compared with those without GDNF transgene.
CONCLUSIONS: Optic nerve could regenerate by peripheral nerve transplantation and GDNF gene transfer.
METHODS: Optic nerve was transected about 2 mm posterior to the eye to establish experimental models of optic neuropathy. Sciatic nerve was sutured to the sheath of injury optic nerve by a 10-0 nylon, pcDNA3-GDNF was smeared to the joint and injected to the vitreous cavity. The regenerated retinal ganglion cells axons were observed by HRP. The retina and optic nerve were observed by pathohistological methods.
RESULTS: Some retinal ganglion cells with regenerated axons could be seen a week after transplantation with large cell bodies. The cells could be identified by HRP. The regenerated nerve fibers grew to the transplanted sciatic nerve. Then the number of retinal ganglion cells with regenerated axons increased with time going. Only a few regenerated retinal ganglion cells could be seen two months after transplantation. The large retinal ganglion cells were seen to have plenty of cytoplasms and be in an active state under electron microscope. Some nerve fibers could be seen in the joint. Sciatic nerve transplantation combined with GDNF gene therapy could increase the amount of retinal ganglion cells with regenerated axons compared with those without GDNF transgene.
CONCLUSIONS: Optic nerve could regenerate by peripheral nerve transplantation and GDNF gene transfer.