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Defect-related luminescent nanostructured hydroxyapatite promotes mineralization through both intracellular and extracellular pathways

机译:缺陷相关的发光纳米结构羟基磷灰石通过细胞内和细胞外途径促进矿化

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摘要

Hydroxyapatite (HAP) is a widely used biomaterial for bone tissue substitution due to its chemical similarity with the natural bone. Defect-related luminescent HAP materials have the same chemical composition as normal HAP and excellent biocompatibility. However, only few works have focused on the defect-related luminescent HAP materials on bone regeneration. In this work, we systematically investigated the bone regeneration pathway induced by nanostructured particles using defect-related luminescent hydroxyapatite (S2) materials. We monitored the subcellular distribution and location of S2 during osteoblast differentiation with the property of defect-related luminescence. Nano-scale S2 could be internalized by osteoblasts (OBs) via caveolae-mediated endocytosis and macropinocytosis. S2 incorporated into the lysosomes dissolved and released calcium ions for the formation of mineralized nodules. Extracellular S2 also promoted bone regeneration as a nucleation site. Taken together, the physical properties of hydroxyapatite control the bone regeneration pathway in osteoblasts.
机译:羟基磷灰石(HAP)是用于骨组织置换的广泛使用的生物材料,因为它与天然骨的化学相似性。缺陷相关的发光HAP材料具有相同的化学组成为正常HAP和优良的生物相容性。然而,只有少数作品都集中在骨再生的缺陷相关的发光材料HAP。在这项工作中,我们系统地研究了通过使用缺陷相关的发光羟基磷灰石(S2)的材料的纳米结构的颗粒引起的骨再生通路。我们与缺陷相关的发光的特性成骨细胞分化过程中监测S2的亚细胞分布和位置。纳米级S2可以由成骨细胞内化(OBS)经由小窝介导的内吞作用和大胞饮。 S2结合到溶解和释放的钙离子矿化结节形成溶酶体。外S2也促进骨再生成核位点。两者合计,羟基磷灰石的物理性质控制在成骨细胞的骨再生通路。

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    《RSC Advances 》 |2019年第62期| 共9页
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  • 正文语种 eng
  • 中图分类 化学 ;
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