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Tissue remodeling in the intervertebral disc: Response to dynamic loading and growth factors.

机译:椎间盘组织重塑:对动态负荷和生长因子的反应。

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摘要

Disc degeneration is a chronic remodeling process that results in alterations of matrix composition and decreased cellularity. The objective of this work was to explore two important topics related to disc degeneration: (1) the role of mechanical loading in alterations of disc biology, and (2) the potential to repair degenerated discs. The first study tested the hypothesis that dynamic mechanical forces are important regulators of disc cellularity and matrix synthesis. The second study hypothesized that exogenous growth factors can stimulate regenerative remodeling in the degenerated disc in vivo.; To study dynamic forces, a murine model of dynamic loading was developed that used an external loading device to cyclically compress a single disc in the tail. Dynamic loading induced differential effects that depended on frequency and stress. The results suggested a tolerance to loading above which evidence of both an anabolic response (increased proteoglycan content and matrix gene expression) and a degenerative response (cell death) were found. Finite element modeling suggested that the responses might be due to variation of strain environment.; The effects of exogenous growth factors on degenerated discs were studied in vivo using a murine model of compression-induced degeneration. Degenerated discs were given single or multiple injections of GDF-5, TGF-β, IGF-1, bFGF, or saline as control and analyzed either one week or four weeks after treatment. In some growth factor treated discs, expansion of inner annular chondrocyte populations into the nucleus were observed. The results indicated that annular chondrocytes may be responsive to some growth factors in vivo, and that GDF-5 and TGF-β may be mitogens for annular chondrocytes.; In summary, this work provides new knowledge of the mechanisms of tissue remodeling in situ in the intervertebral disc. The results have implications in the prevention and treatment of disc degeneration. The responses to dynamic mechanical forces suggest that loading conditions may be optimized to promote maintenance of normal structure and function. The cellular response to growth factors observed in degenerated discs demonstrates the possibility of their use in new therapeutic modalities for repair.
机译:椎间盘退变是一种慢性重塑过程,会导致基质组成改变和细胞减少。这项工作的目的是探讨与椎间盘退变有关的两个重要主题:(1)机械负荷在椎间盘生物学改变中的作用,以及(2)修复退变椎间盘的潜力。第一项研究检验了以下假设:动态机械力是椎间盘细胞性和基质合成的重要调节剂。第二项研究假设外源性生长因子可以刺激体内退化的椎间盘的再生重塑。为了研究动力,开发了一种小鼠动态负荷模型,该模型使用外部负荷装置循环压缩尾巴中的单个椎间盘。动态加载引起取决于频率和应力的微分效应。结果表明对负载的耐受性,在该耐受性以上,发现了同化反应(蛋白聚糖含量和基质基因表达增加)和变性反应(细胞死亡)的证据。有限元建模表明,响应可能是由于应变环境的变化而引起的。使用小鼠压迫性变性模型对体内外源性生长因子对椎间盘的影响进行了体内研究。对退化的椎间盘单次或多次注射GDF-5,TGF-β,IGF-1,bFGF或生理盐水作为对照,并在治疗后1周或4周进行分析。在一些生长因子处理过的椎间盘中,观察到内环形软骨细胞群向核内扩展。结果表明,环形软骨细胞可能对体内某些生长因子具有响应性,而GDF-5和TGF-β可能是环形软骨细胞的促分裂原。总之,这项工作为椎间盘原位重构提供了新的知识。结果对椎间盘退变的预防和治疗具有重要意义。对动态机械力的响应表明,可以优化加载条件以促进正常结构和功能的维持。在退化的椎间盘中观察到的细胞对生长因子的反应证明了它们可用于新的修复治疗方法的可能性。

著录项

  • 作者单位

    University of California, San Francisco with the University of California, Berkeley.;

  • 授予单位 University of California, San Francisco with the University of California, Berkeley.;
  • 学科 Engineering Biomedical.; Health Sciences Radiology.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 96 p.
  • 总页数 96
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物医学工程;预防医学、卫生学;
  • 关键词

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