首页> 美国卫生研究院文献>Springer Open Choice >Ruffled border formation on a CaP-free substrate: A first step towards osteoclast-recruiting bone-grafts materials able to re-establish bone turn-over
【2h】

Ruffled border formation on a CaP-free substrate: A first step towards osteoclast-recruiting bone-grafts materials able to re-establish bone turn-over

机译:在不含CaP的基材上形成皱纹边界:迈向破骨细胞招募能够重建骨翻转的骨移植材料的第一步

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Osteoclasts are large multinucleated giant cells that actively resorb bone during the physiological bone turnover (BTO), which is the continuous cycle of bone resorption (by osteoclasts) followed by new bone formation (by osteoblasts). Osteoclasts secrete chemotactic signals to recruit cells for regeneration of vasculature and bone. We hypothesize that a biomaterial that attracts osteoclasts and re-establishes BTO will induce a better healing response than currently used bone graft materials. While the majority of bone regeneration efforts have focused on maximizing bone deposition, the novelty in this approach is the focus on stimulating osteoclastic resorption as the starter for BTO and its concurrent new vascularized bone formation. A biodegradable tyrosine-derived polycarbonate, E1001(1k), was chosen as the polymer base due to its ability to support bone regeneration in vivo. The polymer was functionalized with a RGD peptide or collagen I, or blended with β-tricalcium phosphate. Osteoclast attachment and early stages of active resorption were observed on all substrates. The transparency of E1001(1k) in combination with high resolution confocal imaging enabled visualization of morphological features of osteoclast activation such as the formation of the “actin ring” and the “ruffled border”, which previously required destructive forms of imaging such as transmission electron microscopy. The significance of these results is twofold: (1) E1001(1k) is suitable for osteoclast attachment and supports osteoclast maturation, making it a base polymer that can be further modified to optimize stimulation of BTO and (2) the transparency of this polymer makes it a suitable analytical tool for studying osteoclast behavior.
机译:破骨细胞是大型的多核巨细胞,在生理性骨转换(BTO)期间主动吸收骨,BTO是骨吸收(通过破骨细胞)然后是新骨形成(通过成骨细胞)的连续循环。破骨细胞分泌趋化信号以募集细胞,用于血管和骨骼的再生。我们假设,一种吸引破骨细胞并重新建立BTO的生物材料将比目前使用的骨移植材料产生更好的愈合反应。尽管大多数骨骼再生工作都集中在最大程度地增加骨骼沉积上,但是这种方法的新颖之处在于,它以刺激破骨细胞吸收作为BTO及其同时出现的新血管化骨形成的起点。由于其在体内支持骨骼再生的能力,因此将可生物降解的酪氨酸衍生的聚碳酸酯E1001(1k)选作聚合物基础。该聚合物用RGD肽或胶原蛋白I官能化,或与β-磷酸三钙共混。在所有底物上均观察到破骨细胞的附着和主动吸收的早期阶段。 E1001(1k)的透明性与高分辨率共聚焦成像相结合,可以可视化破骨细胞活化的形态特征,例如“肌动蛋白环”和“皱边”的形成,而以前需要破坏性的成像形式,例如透射电子显微镜检查。这些结果的意义有两方面:(1)E1001(1k)适合破骨细胞附着并支持破骨细胞成熟,使其成为基础聚合物,可以进一步修饰以优化BTO的刺激作用;(2)该聚合物的透明性它是研究破骨细胞行为的合适分析工具。

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号