首页> 外文会议>Biomaterials science: processing, properties and applications II. >INFLUENCES OF SR, ZN AND MG DOPANTS ON OSTEOCLAST DIFFERENTIATION AND RESORPTION
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INFLUENCES OF SR, ZN AND MG DOPANTS ON OSTEOCLAST DIFFERENTIATION AND RESORPTION

机译:SR,ZN和MG掺杂对破骨细胞分化和吸收的影响

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摘要

Osteoclasts, the bone resorbing cells, are specialized macrophages generating from differentiation of mononuclear cells. In this research strontium (Sr), magnesium (Mg) and zinc (Zn) substituted beta-tricalcium phosphate (β-TCP) on differentiation of mononuclear cells into osteoclasts and its resorptive activity were studied. 1.0 wt% Sr, 1.0 wt% Mg, and 0.25 wt% Zn doped β-TCP were prepared by sintering at 1250 ℃. Osteoclast differentiation and resorption was studied in vitro using RAW 264.7 precursor cell, supplemented with receptor activator of nuclear factor kβ ligand (RANKL). Formation of osteoclast cells were monitored by field emission scanning electron microscope (FESEM) and immunohistochemical analysis. Formation of osteoclasts were noticed on pure, Sr doped and Zn doped β-TCP samples after 8 days of culture. However, no such osteoclast formation was found on Mg doped β-TCP samples. Cells on the substrates surface expressed specific osteoclast markers such as; actin ring, multiple nucleus, and vitronectin receptor. Immunohistochemical analysis indicated that matured osteoclasts were formed on β-TCP, Sr, and Zn doped samples after 14 days of culture whereas it took 21 days to form matured osteoclasts on Mg doped samples. Differentiated osteoclasts successfully resorbed β-TCP samples which increased for Zn doped samples and decreased for Sr doped samples. Mg doped β-TCP samples initially restricted osteoclast differentiation, however, once formed showed prominent resorption lacunae formation.
机译:破骨细胞,即骨吸收细胞,是由单核细胞分化产生的专门的巨噬细胞。本研究研究了锶(Sr),镁(Mg)和锌(Zn)取代的β-磷酸三钙(β-TCP)对单核细胞分化为破骨细胞及其吸收活性的影响。通过在1250℃下烧结制备1.0 wt%Sr,1.0 wt%Mg和0.25 wt%Zn掺杂的β-TCP。使用补充有核因子kβ配体的受体激活剂(RANKL)的RAW 264.7前体细胞体外研究了破骨细胞的分化和吸收。通过场发射扫描电子显微镜(FESEM)和免疫组织化学分析监测破骨细胞的形成。培养8天后,在纯,掺Sr和掺锌的β-TCP样品上注意到破骨细胞的形成。但是,在掺Mg的β-TCP样品中未发现破骨细胞形成。基质表面上的细胞表达特定的破骨细胞标记,例如;肌动蛋白环,多核和玻连蛋白受体。免疫组织化学分析表明,培养14天后,在掺有β-TCP,Sr和Zn的样品上形成了成熟的破骨细胞,而在掺Mg的样品上花费了21天才形成成熟的破骨细胞。分化的破骨细胞成功地吸收了β-TCP样品,对于Zn掺杂的样品来说增加,而Sr掺杂的样品则减少。镁掺杂的β-TCP样品最初限制了破骨细胞的分化,但是一旦形成,就会显示出明显的吸收性腔隙形成。

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  • 来源
  • 会议地点 Columbus OH(US);Columbus OH(US);Columbus OH(US)
  • 作者单位

    W. M. Keck Biomedical Materials Research Laboratory School of Mechanical and Materials Engineering Washington State University, Pullman, WA 99164, USA;

    W. M. Keck Biomedical Materials Research Laboratory School of Mechanical and Materials Engineering Washington State University, Pullman, WA 99164, USA;

    W. M. Keck Biomedical Materials Research Laboratory School of Mechanical and Materials Engineering Washington State University, Pullman, WA 99164, USA;

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  • 正文语种 eng
  • 中图分类 生物材料学;生物材料学;
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