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首页> 外文期刊>Annals of the New York Academy of Sciences >Clinical Biophysics: The Promotion of Skeletal Repair by Physical Forces
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Clinical Biophysics: The Promotion of Skeletal Repair by Physical Forces

机译:临床生物物理学:物理力量促进骨骼修复

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摘要

Skeletal tissues respond to the physical demands of their environment by altering the synthesis and organization of the extracellular matrix. These observations have major implications for how physical environmental demands result in the clinical observations of atrophy and hypertrophy, and how manipulation of the physical environment can be used therapeutically to stimulate repair. Electrical stimulation will be considered as a paradigm of how musculoskeletal tissues respond to physical stimuli. A model of demineralized bone matrix-induced endo-chondral ossification has been used because it epitomizes the cell biology of endochondral bone formation in a temporally consistent way. We have studied cartilage and bone matrix production, the temporal locus of cell responsiveness, signal dosimetry, and the synthesis of signaling cytokines (TGF-β) using biochemical, immunohistochemical, and molecular techniques. Exposure to certain electrical environments enhances chondro-cyte differentiation reflected as a temporal acceleration and quantitative increase of cartilage extracellular matrix, earlier onset of osteogenesis, and more mature trabecular bone. The cell pool competent to respond resides in the mesenchymal stage. The enhancement in chondrogenesis is associated with an increase in TGF-β synthesis mediated at least in part by binding of the transcription factor AP-1 and may be modulated specifically by phosphorylation of JNK. The clinical practice of orthopedics has empirically created a variety of biophysical environments in attempts to optimize skeletal repair. We are beginning to understand the biological effects of biophysical stimulation and are now poised to replace empiricism with treatment paradigms based upon physiologic understandings of dose and biologic response.
机译:骨骼组织通过改变细胞外基质的合成和组织来响应其环境的物理需求。这些观察结果对物理环境需求如何导致萎缩和肥大的临床观察以及如何对物理环境进行治疗可用于治疗性刺激修复具有重大意义。电刺激将被视为肌肉骨骼组织如何对物理刺激做出反应的范例。使用去矿质骨基质诱导的软骨内骨化的模型是因为它以时间上一致的方式概括了软骨内骨形成的细胞生物学。我们已经使用生化,免疫组织化学和分子技术研究了软骨和骨基质的产生,细胞反应性的时间轨迹,信号剂量测定以及信号传导细胞因子(TGF-β)的合成。暴露于某些电环境会增强软骨细胞的分化,这表现为软骨细胞外基质的时间加速和定量增加,成骨作用的更早发作以及更成熟的小梁骨。能反应的细胞池位于间充质阶段。软骨形成的增强与至少部分地通过转录因子AP-1的结合介导的TGF-β合成的增加有关,并且可以通过JNK的磷酸化来特异性地调节。骨科的临床实践经验性地创建了各种生物物理环境,以优化骨骼修复。我们开始了解生物物理刺激的生物学效应,现在准备根据对剂量和生物学反应的生理学理解,用治疗范例代替经验主义。

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