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脉冲低强度超声在琼脂糖和单层培养物中刺激软骨细胞基质合成的潜力。

The potential of pulsed low intensity ultrasound to stimulate chondrocytes matrix synthesis in agarose and monolayer cultures.

机构信息

School of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London, E1 4NS, UK.

出版信息

Med Biol Eng Comput. 2010 Dec;48(12):1215-22. doi: 10.1007/s11517-010-0681-3. Epub 2010 Oct 12.

Abstract

Pulsed low intensity ultrasound (PLIUS) has been used successfully for bone fracture repair and has therefore been suggested for cartilage regeneration. However, previous in vitro studies with chondrocytes show conflicting results as to the effect of PLIUS on the elaboration of extracellular matrix. This study tests the hypothesis that PLIUS, applied for 20 min/day, stimulates the synthesis of sulphated glycosaminoglycan (sGAG) by adult bovine articular chondrocytes cultured in either monolayer or agarose constructs. For both culture models, PLIUS at either 30 or 100 mW/cm(2) intensity had no net effect on the total sGAG content. Although PLIUS at 100 mW/cm(2) did induce a 20% increase in sGAG content at day 2 of culture in agarose, this response was lost by day 5. Intensities of 200 and 300 mW/cm(2) resulted in cell death probably due to heating from the ultrasound transducers. The lack of a sustained up-regulation of sGAG synthesis may reflect the suggestion that PLIUS only induces a stimulatory effect in the presence of a tissue injury response. These results suggest that PLIUS has a limited potential to provide an effective method of stimulating matrix production as part of a tissue engineering strategy for cartilage repair.

摘要

脉冲低强度超声(PLIUS)已成功用于骨折修复,因此被建议用于软骨再生。然而,先前的软骨细胞体外研究结果显示,PLIUS 对细胞外基质的产生有相互矛盾的影响。本研究检验了以下假设:每天应用 20 分钟的 PLIUS 可刺激单层或琼脂糖构建体中培养的成年牛关节软骨细胞合成硫酸化糖胺聚糖(sGAG)。对于这两种培养模型,强度为 30 或 100 mW/cm(2) 的 PLIUS 对总 sGAG 含量均无净影响。尽管在琼脂糖中培养的第 2 天,100 mW/cm(2) 的 PLIUS 可诱导 sGAG 含量增加 20%,但到第 5 天这种反应就消失了。200 和 300 mW/cm(2) 的强度可能导致细胞死亡,这可能是由于超声换能器的加热所致。sGAG 合成的持续上调不足可能反映了这样一种观点,即只有在组织损伤反应存在的情况下,PLIUS 才会诱导刺激作用。这些结果表明,PLIUS 刺激基质产生的潜力有限,可能无法成为软骨修复组织工程策略的有效方法。

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