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壳聚糖-氧化石墨烯 3D 支架作为促进临界尺寸小鼠颅骨缺损骨再生的有前途的工具。

Chitosan-Graphene Oxide 3D scaffolds as Promising Tools for Bone Regeneration in Critical-Size Mouse Calvarial Defects.

机构信息

Department of Histology, Faculty of Medicine, Vasile Goldis Western University of Arad, 86 Rebreanu, 310414, Arad, Romania.

Department of Experimental and Applied Biology, Institute of Life Sciences, Vasile Goldis Western University of Arad, 86 Rebreanu, 310414, Arad, Romania.

出版信息

Sci Rep. 2017 Nov 30;7(1):16641. doi: 10.1038/s41598-017-16599-5.

Abstract

Limited self-regenerating capacity of human skeleton makes the reconstruction of critical size bone defect a significant challenge for clinical practice. Aimed for regenerating bone tissues, this study was designed to investigate osteogenic differentiation, along with bone repair capacity of 3D chitosan (CHT) scaffolds enriched with graphene oxide (GO) in critical-sized mouse calvarial defect. Histopathological/histomorphometry and scanning electron microscopy(SEM) analysis of the implants revealed larger amount of new bone in the CHT/GO-filled defects compared with CHT alone (p < 0.001). When combined with GO, CHT scaffolds synergistically promoted the increase of alkaline phosphatase activity both in vitro and in vivo experiments. This enhanced osteogenesis was corroborated with increased expression of bone morphogenetic protein (BMP) and Runx-2 up to week 4 post-implantation, which showed that GO facilitates the differentiation of osteoprogenitor cells. Meanwhile, osteogenesis was promoted by GO at the late stage as well, as indicated by the up-regulation of osteopontin and osteocalcin at week 8 and overexpressed at week 18, for both markers. Our data suggest that CHT/GO biomaterial could represent a promising tool for the reconstruction of large bone defects, without using exogenous living cells or growth factors.

摘要

人类骨骼的自我再生能力有限,这使得重建临界尺寸的骨缺损成为临床实践中的一个重大挑战。本研究旨在探讨富含氧化石墨烯(GO)的 3D 壳聚糖(CHT)支架的成骨分化和骨修复能力,以用于临界尺寸小鼠颅骨缺损的再生。植入物的组织病理学/组织形态计量学和扫描电子显微镜(SEM)分析显示,与单独的 CHT 相比,CHT/GO 填充的缺损中有更多的新骨(p<0.001)。当与 GO 结合时,CHT 支架在体外和体内实验中协同促进碱性磷酸酶活性的增加。这种增强的成骨作用得到了骨形态发生蛋白(BMP)和 Runx-2 表达的证实,直到植入后第 4 周,这表明 GO 促进了成骨前体细胞的分化。同时,GO 也在后期促进了成骨作用,如第 8 周骨桥蛋白和骨钙素的上调以及第 18 周的过表达,这两种标志物均如此。我们的数据表明,CHT/GO 生物材料可能是一种有前途的工具,可用于重建大的骨缺损,而无需使用外源性活细胞或生长因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a38/5709492/f52ee435bf83/41598_2017_16599_Fig1_HTML.jpg

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