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分析纳米拓扑二氧化钛表面的破骨细胞/成骨细胞形成。

Analysis of Osteoclastogenesis/Osteoblastogenesis on Nanotopographical Titania Surfaces.

机构信息

Centre for Cell Engineering, Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, UK.

Biomaterials Engineering Group, School of Oral and Dental Sciences, University of Bristol, Lower Maudlin Street, Bristol, BS1 2LY, UK.

出版信息

Adv Healthc Mater. 2016 Apr 20;5(8):947-55. doi: 10.1002/adhm.201500664. Epub 2016 Feb 18.

DOI:10.1002/adhm.201500664
PMID:26890261
Abstract

A focus of orthopedic research is to improve osteointegration and outcomes of joint replacement. Material surface topography has been shown to alter cell adhesion, proliferation, and growth. The use of nanotopographical features to promote cell adhesion and bone formation is hoped to improve osteointegration and clinical outcomes. Use of block-copolymer self-assembled nanopatterns allows nanopillars to form via templated anodization with control over height and order, which has been shown to be of cellular importance. This project assesses the outcome of a human bone marrow-derived co-culture of adherent osteoprogenitors and osteoclast progenitors on polished titania and titania patterned with 15 nm nanopillars, fabricated by a block-copolymer templated anodization technique. Substrate implantation in rabbit femurs is performed to confirm the in vivo bone/implant integration. Quantitative and qualitative results demonstrate increased osteogenesis on the nanopillar substrate with scanning electron microscopy, histochemical staining, and real-time quantitative reverse-transcription polymerase chain reaction analysis performed. Osteoblast/osteoclast co-culture analysis shows an increase in osteoblastogenesis-related gene expression and reduction in osteoclastogenesis. Supporting this in vitro finding, in vivo implantation of substrates in rabbit femora indicates increased implant/bone contact by ≈20%. These favorable osteogenic characteristics demonstrate the potential of 15 nm titania nanopillars fabricated by the block-copolymer templated anodization technique.

摘要

骨科研究的重点是改善骨整合和关节置换的效果。已经证明材料表面形貌可以改变细胞的黏附、增殖和生长。使用纳米形貌特征来促进细胞黏附和骨形成有望改善骨整合和临床效果。使用嵌段共聚物自组装纳米图案可以通过模板阳极氧化形成纳米柱,从而控制高度和有序性,这已经被证明对细胞很重要。该项目评估了在经过抛光的二氧化钛和通过嵌段共聚物模板阳极氧化技术制造的具有 15nm 纳米柱的二氧化钛上,人类骨髓来源的黏附性成骨前体细胞和破骨细胞前体细胞的共培养的结果。通过在兔股骨中植入基底来确认体内骨/植入物的整合。通过扫描电子显微镜、组织化学染色和实时定量逆转录聚合酶链反应分析进行定量和定性研究,结果表明纳米柱基底上的成骨作用增加。成骨细胞/破骨细胞共培养分析显示成骨相关基因表达增加,破骨细胞生成减少。体外植入实验表明,体内植入基底后,植入物/骨接触增加了约 20%。这些有利的成骨特性表明,通过嵌段共聚物模板阳极氧化技术制造的 15nm 二氧化钛纳米柱具有潜力。

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