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Tissue engineering strategies for neural tissue using adult stem cells.

机译:使用成人干细胞的神经组织的组织工程策略。

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摘要

The inability of the spinal cord to repair and regenerate following injury has been attributed, in part, to a lack of sufficient stem cells that can proliferate and regenerate the cellular phenotypes found in nervous tissue. Stem cells from various sources such as embryonic, neural tissue, and bone marrow, have been tested for recovery of function in the injured spinal cord. Limitations exist in terms of availability, suitability, or potential to differentiate and integrate with host tissure in a functional manner. In this study, human adult stem cells were derived from skeletal muscle and induced into all three of the neural lineages in vitro, by two different methods. Once it was determined that human adult stem cells could differentiate into neural phenotypes, the adult stem cells became a possible treatment for central nervous system injury. The NYU model of spinal cord contusion injury was produced in rats with a weight drop device at T10. Cultured adult stem cells, isolated from the skeletal muscle of an adult ROSA (LacZ+) mouse, were injected into the spinal cord injury site (3 x 105 cells in 10 mul saline). Locomotor function was determined for 6 weeks following injury with the BBB locomotor scale. Transplanted adults stem cells and neural phenotypes were identified immunohistochemically in longitudinal spinal cord sections. Locomotor function was significantly greater in the adult stem cell-injected rats (n=11) than in the saline vehicle-injected (n=6) control rats. The final mean BBB scores for the adult stem cell-injected rats was 9.1 and the final mean BBB scores for the saline injected rats was 5.0 (P0.05). Double fluorescent immunolabeling indicated the presence of adult stem cells expressing markers for neurons, astrocytes, and oligodendrocytes as well as undifferentiated adult stem cells. These results may indicate that adult stem cell implantation is a potential tissue engineering treatment for paralysis due to spinal cord injury.
机译:脊髓不能在损伤后修复和再生的部分原因是缺乏足够的干细胞,这些干细胞可以增殖和再生神经组织中发现的细胞表型。已经测试了来自各种来源(例如胚胎,神经组织和骨髓)的干细胞在受损脊髓中的功能恢复。在可用性,适用性或以功能性方式区分和整合宿主的潜力方面存在局限性。在这项研究中,人类成体干细胞源自骨骼肌,并通过两种不同的方法在体外被诱导进入所有三个神经系。一旦确定人类成年干细胞可以分化为神经表型,该成年干细胞就成为治疗中枢神经系统损伤的一种可能方法。在T10用减重装置在大鼠中产生了脊髓挫伤性NYU模型。从成年ROSA(LacZ +)小鼠的骨骼肌中分离出的成年干细胞被注射到脊髓损伤部位(在10毫升盐水中3 x 105个细胞)。用BBB运动量表在受伤后6周确定运动功能。移植的成人干细胞和神经表型在纵向脊髓切片中进行了免疫组织化学鉴定。成年干细胞注射大鼠(n = 11)的运动功能明显大于生理盐水注射(n = 6)对照大鼠。成年干细胞注射大鼠的最终平均BBB评分为9.1,盐水注射大鼠的最终平均BBB评分为5.0(P <0.05)。双重荧光免疫标记表明存在表达神经元,星形胶质细胞和少突胶质细胞标记的成年干细胞以及未分化的成年干细胞。这些结果可能表明,成年干细胞植入是潜在的组织工程治疗脊髓损伤引起的瘫痪。

著录项

  • 作者

    Schultz, Sherri S.;

  • 作者单位

    New York Medical College.;

  • 授予单位 New York Medical College.;
  • 学科 Biology Neuroscience.;Biology Cell.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 166 p.
  • 总页数 166
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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