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Zinc silicate mineral-coated scaffold improved in vitro osteogenic differentiation of equine adipose-derived mesenchymal stem cells

机译:硅酸盐矿棉矿棉支架改善了马脂肪衍生的间充质干细胞的体外成骨分化

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In current study we aimed to coat the PLLA scaffold with zinc (Zn) silicate mineral nanoparticles. Then, using equine adipose-derived stem cells (ASCs) we intended to compare the osteogenic induction potency of Zn silicate mineral-coated PLLA scaffold with uncoated PLLA scaffold and tissue culture plastic (TCPS). Adipose tissues were collected from 3 horses, and isolation of ASCs was achieved by enzymatic digestion. PLLA scaffold was successfully prepared using a phase separation method and coated with Zn silicate mineral nanoparticles. The coating efficiency was then characterized by scanning electron microscopy and further evaluated with the application of fourier transform infrared microscopic imaging. Viability and growth characteristics of ASCs on TCPS, uncoated and coated PLAA scaffolds were investigated by MTT assay Alizarin Red staining was performed for determination of calcium deposition following the osteogenic induction. Furthermore, other common osteogenic markers such as alkaline phosphatase (ALP) activity, calcium content, as well as osteogenic (Runx2, ALP, osteonectin, and collagen I) marker genes were also evaluated. Our data showed that Zn silicate mineral nanoparticles was coated successfully on PLLA scaffold and such scaffold had no detrimental effect on cell growth rate as indicated by MTT assay. Moreover, ASCs that differentiated on Zn silicate mineral-coated PLLA scaffold indicated higher ALP activity, more calcium content, and higher expression of bone-related genes than that on uncoated PLLA scaffold and TCPS. Adequate proliferation rate and higher expression of osteogenic markers of stem cells, provides this scaffold as a suitable substrate to support proliferation and differentiation of ASCs in equine.
机译:在目前的研究中,我们的目标是用锌(Zn)硅酸盐矿物纳米颗粒涂覆PLLA支架。然后,使用马脂肪衍生的干细胞(ASCS),我们旨在比较Zn硅酸盐矿物涂覆的PLLA支架与未涂覆的PLLA支架和组织培养塑料(TCP)的溶血性诱导效力。从3匹马收集脂肪组织,通过酶消化来实现ASC的分离。使用相分离方法成功制备PLLA支架并用Zn硅酸盐矿物纳米颗粒涂覆。然后通过扫描电子显微镜表征涂料效率并进一步评估傅里叶变换红外微观成像。通过MTT测定茜素红染色研究了ASCPS对TCPS,未涂层和涂覆的PLAA支架的可活力和生长特性,进行了溶血性诱导后测定钙沉积的测定。此外,还评估了其他常见的骨质骨质原 - 诸如碱性磷酸酶(ALP)活性,钙含量以及骨质发生(RUNX2,ALP,Osteoncencectin和胶原I)标志物基因。我们的数据表明,Zn硅酸盐矿物纳米颗粒在PLLA支架上成功涂覆,并且这种支架对细胞生长速率没有不利影响,如MTT测定所示。此外,在Zn硅酸盐矿物涂覆的PLLA支架上分化的ASCS表示较高的ALP活性,更多的钙含量和骨相关基因的更高表达,而不是未涂覆的PLLA支架和TCP。适当的增殖率和干细胞的成骨标志物的高表达,将该支架提供为合适的基材,以载有QUACE中的ASCS的增殖和分化。

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