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成年大鼠实验性脑损伤后的胎儿皮质移植

Fetal cortical transplants in adult rats subjected to experimental brain injury.

作者信息

Soares H, McIntosh T K

机构信息

Department of Surgery, University of Connecticut Health Center, Farmington 06032.

出版信息

J Neural Transplant Plast. 1991;2(3-4):207-20. doi: 10.1155/NP.1991.207.

Abstract

Fetal cortical tissue was injected into injured adult rat brains following concussive fluid percussion (FP) brain injury. Rats subjected to moderate FP injury received E16 cortex transplant injections into lesioned motor cortex 2 days, 1 week, 2 weeks, and 4 weeks post injury. Histological assessment of transplant survival and integration was based upon Nissl staining, glial fibrillary acidic protein (GFAP) immunocytochemistry, and staining for acetylcholinesterase. In addition to histological analysis, the ability of the transplants to attenuate neurological motor deficits associated with concussive FP brain injury was also tested. Three subgroups of rats receiving transplant 1 week, 2 weeks, and 4 weeks post injury were chosen for evaluation of neurological motor function. Fetal cortical tissue injected into the injury site 4 weeks post injury failed to incorporate with injured host brain, did not affect glial scar formation, and exhibited extensive GFAP immunoreactivity. No improvement in neurological motor function was observed in animals receiving transplants 4 weeks post injury. Conversely, transplants injected 2 days, 1 week, or 2 weeks post injury survived, incorporated with host brain, exhibited little GFAP immunoreactivity, and successfully attenuated glial scarring. However, no significant improvement in motor function was observed at the one week or two week time points. The inability of the transplants to attenuate motor function may indicate inappropriate host/transplant interaction. Our results demonstrate that there exists a temporal window in which fetal cortical transplants can attenuate glial scarring as well as be successfully incorporated into host brains following FP injury.

摘要

在流体冲击(FP)性脑损伤后,将胎儿皮质组织注射到成年大鼠的受伤大脑中。遭受中度FP损伤的大鼠在受伤后2天、1周、2周和4周,将胚胎第16天的皮质移植到受损的运动皮质中。基于尼氏染色、胶质纤维酸性蛋白(GFAP)免疫细胞化学和乙酰胆碱酯酶染色对移植组织的存活和整合进行组织学评估。除了组织学分析外,还测试了移植组织减轻与FP性脑震荡损伤相关的神经运动功能缺损的能力。选择在受伤后1周、2周和4周接受移植的三组大鼠亚组来评估神经运动功能。在受伤后4周注射到损伤部位的胎儿皮质组织未能与受伤的宿主脑融合,不影响胶质瘢痕形成,并表现出广泛的GFAP免疫反应性。在受伤后4周接受移植的动物中未观察到神经运动功能的改善。相反,在受伤后2天、1周或2周注射的移植组织存活下来,与宿主脑融合,表现出很少的GFAP免疫反应性,并成功减轻了胶质瘢痕形成。然而,在1周或2周时间点未观察到运动功能有显著改善。移植组织无法减轻运动功能可能表明宿主/移植组织相互作用不当。我们的结果表明,存在一个时间窗,在此期间胎儿皮质移植可以减轻胶质瘢痕形成,并在FP损伤后成功整合到宿主脑中。

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