Hoovler D W, Wrathall J R
Department of Anatomy and Cell Biology, Georgetown University School of Medicine, Washington, DC 20007.
Acta Neuropathol. 1991;81(3):303-11. doi: 10.1007/BF00305872.
Implants of various types of neuronal and nonneuronal tissue have shown promise for the amelioration of certain disorders of the adult mammalian brain. Implants may also have therapeutic potential for some lesions of the spinal cord. To examine the feasibility of implantation for clinically relevant spinal cord injuries, we have implanted cells into injury sites produced by a well-characterized and standardized rat model of contusive injury. To reduce the possibility of the implantation procedure itself causing damage to the spinal cord, the tissue was dissociated and a suspension of cells introduced into the cord via a small bore needle. To test the implantation procedure, dissociated adult rat dorsal root ganglia were used because of the ease with which these neurons could be distinguished after implantation. The extent to which functional deficits were produced or exacerbated by the implantation procedure was assessed by behavioral tests of groups of rats that had been implanted (implant controls), contused (injury only) or contused and implanted (injury-implant). Survival of the implanted neurons was assessed by quantitative morphological analysis of histological sections taken through the injury/implant sites at different times following injury. In addition, the histopathology of the contusive injury sites was compared for rats that had or had not received immediate or delayed implants. Results indicated that cell suspensions could be implanted into the spinal cord without causing a functional deficit in an otherwise uninjured animal or exacerbating a standardized incomplete contusive injury. Implanted neurons survived for at least 4 weeks in all contusion sites whether implantation was performed immediately following injury or after a delay of 1 week.(ABSTRACT TRUNCATED AT 250 WORDS)
各种类型的神经元和非神经元组织植入物已显示出改善成年哺乳动物脑部某些疾病的前景。植入物对脊髓的一些损伤可能也具有治疗潜力。为了研究植入治疗临床相关脊髓损伤的可行性,我们将细胞植入由一种特征明确且标准化的大鼠挫伤性损伤模型所造成的损伤部位。为了降低植入手术本身对脊髓造成损伤的可能性,将组织解离,并通过细针将细胞悬液注入脊髓。为了测试植入手术,使用解离的成年大鼠背根神经节,因为这些神经元在植入后易于识别。通过对已植入(植入对照组)、挫伤(仅损伤组)或挫伤并植入(损伤 - 植入组)的大鼠组进行行为测试,评估植入手术导致或加重功能缺陷的程度。通过对损伤后不同时间取自损伤/植入部位的组织切片进行定量形态分析,评估植入神经元的存活情况。此外,比较了接受或未接受即刻或延迟植入的大鼠挫伤损伤部位的组织病理学。结果表明,细胞悬液可以植入脊髓,而不会在原本未受伤的动物中造成功能缺陷,也不会加重标准化的不完全挫伤性损伤。无论在损伤后立即植入还是延迟1周后植入,植入的神经元在所有挫伤部位都存活了至少4周。(摘要截短至250字)