Neuberger T J, Cornbrooks C J, Kromer L F
Department of Anatomy & Neurobiology, University of Vermont, College of Medicine, Burlington 05405.
J Comp Neurol. 1992 Jan 1;315(1):16-33. doi: 10.1002/cne.903150103.
The introduction of transplants consisting of cultured Schwann cells and their associated extracellular matrix (Sc/ECM) into a central nervous system (CNS) lesion cavity facilitates axonal regeneration from injured, adult mammalian neurons with subsequent reinnervation of their appropriate target (Kromer and Cornbrooks: Proceedings of the National Academy of Sciences of the United States of America 82:6330-6334, 1985). In the present study, the effects of a delayed transplantation procedure on the time course of this regenerative response were evaluated. For these experiments, bilateral CNS lesions were created between the septum and hippocampus by removing the fimbria-fornix pathway. Lesion cavities received either no transplants, transplants of collagen, or Sc/ECM transplants at the time the lesion was created or 6 days later. When no transplants or transplants of collagen were used, axonal sprouts extended for very short distances into the lesion cavity. These axons were not preferentially associated with the collagen transplants nor maintained at long post-lesion survival times. In animals that received Sc/ECM transplants, the number of sprouting axons and the progression of axonal growth along the transplants was much more extensive than for the collagen transplants. Although more axons were detected in cavities that received transplants immediately after the fimbria-fornix lesion, axonal regeneration along the transplants was similar regardless of whether there was a delay in transplanting the Schwann cells. By using histochemical techniques to identify acetylcholinesterase (AChE), regenerating AChE-positive axons were first detected in the cavity at 3 days post-transplantation, were associated with the Sc/ECM transplants by 5 days, and crossed the cavity within 8 days post-transplantation. Regenerating, neurofilament-positive axons crossed the CNS-Sc/ECM transplant interfaces in association with laminin-positive, glial fibrillary acidic protein-positive cellular pathways. Upon reaching the caudal end of the Sc/ECM transplant, the cholinergic axons abandoned the transplant and oriented directly toward the adjacent hippocampus. Both the simultaneous and delayed transplantation paradigms demonstrated a similar reinnervation pattern of AChE-positive fibers in the hippocampus, but there was a more rapid penetration and more extensive arborization of fibers in animals receiving the delayed transplants. Cholinergic fibers initially invaded the dentate gyrus molecular layer and hilus between 8 and 14 days post-transplantation. By 45 days post-transplantation, AChE-positive axons were detected throughout the dentate gyrus and regio inferior, but few fibers were present in regio superior of the hippocampus.(ABSTRACT TRUNCATED AT 400 WORDS)
将由培养的施万细胞及其相关细胞外基质(Sc/ECM)组成的移植物引入中枢神经系统(CNS)损伤腔,可促进成年哺乳动物受损神经元的轴突再生,随后重新支配其适当的靶标(克罗默和康布罗克斯:《美国国家科学院院刊》82:6330 - 6334, 1985)。在本研究中,评估了延迟移植程序对这种再生反应时间进程的影响。对于这些实验,通过切除穹窿 - 海马伞通路在隔区和海马之间造成双侧CNS损伤。损伤腔在损伤形成时或6天后接受无移植、胶原移植或Sc/ECM移植。当不使用移植或使用胶原移植时,轴突发芽延伸到损伤腔内的距离非常短。这些轴突与胶原移植无优先关联,也未在损伤后长时间存活期维持。在接受Sc/ECM移植的动物中,发芽轴突的数量以及沿移植的轴突生长进程比胶原移植更为广泛。尽管在穹窿 - 海马伞损伤后立即接受移植的腔中检测到更多轴突,但无论施万细胞移植是否延迟,沿移植的轴突再生相似。通过使用组织化学技术鉴定乙酰胆碱酯酶(AChE),再生的AChE阳性轴突在移植后3天首次在腔中检测到,在5天时与Sc/ECM移植相关联,并在移植后8天内穿过腔。再生的神经丝阳性轴突与层粘连蛋白阳性、胶质纤维酸性蛋白阳性的细胞通路相关联穿过CNS - Sc/ECM移植界面。到达Sc/ECM移植尾端后,胆碱能轴突离开移植并直接朝向相邻海马定向。同时移植和延迟移植模式在海马中均显示出AChE阳性纤维的相似再支配模式,但在接受延迟移植的动物中,纤维的穿透更快且分支更广泛。胆碱能纤维在移植后8至14天最初侵入齿状回分子层和门区。到移植后45天,在整个齿状回和海马下部区域检测到AChE阳性轴突,但海马上部区域存在的纤维很少。(摘要截短至400字)