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氟掺杂对人牙滤泡干细胞(hDFSCs)成骨分化的影响。

Effect of Fluoride Doping in Laponite Nanoplatelets on Osteogenic Differentiation of Human Dental Follicle Stem Cells (hDFSCs).

机构信息

Department of Biomedical engineering, Indian Institute of Technology Hyderabad, Kandi, Telangana, India.

Department of Biosciences and Bioengineering, Indian Institute of Technology Bombay, Powai, Mumbai, Maharashtra, India.

出版信息

Sci Rep. 2019 Jan 29;9(1):915. doi: 10.1038/s41598-018-37327-7.

Abstract

Bioactive nanosilicates are emerging prominent next generation biomaterials due to their intrinsic functional properties such as advanced biochemical and biophysical cues. Recent studies show interesting dose-dependent effect of fluoride ions on the stem cells. Despite of interesting properties of fluoride ions as well as nanosilicate, there is no reported literature on the effect of fluoride-doped nanosilicates on stem cells. We have systematically evaluated the interaction of fluoride nanosilicate platelets (NS + F) with human dental follicle stem cells (hDFSCs) to probe the cytotoxicity, cellular transport (internalization) and osteogenic differentiation capabilities in comparison with already reported nanosilicate platelets without fluoride (NS - F). To understand the osteoinductive and osteoconductive properties of the nanosilicate system, nanosilicate treated hDFSCs are cultured in three different medium namely normal growth medium, osteoconductive medium, and osteoinductive medium up to 21 d. NS + F treated stem cells show higher ALP activity, osteopontin levels and significant alizarin red staining compared to NS - F treated cells. This study highlights that the particles having fluoride additives (NS + F) aid in enhancing the osteogenic differentiation capabilities of hDFSCs thus potential nanobiomaterial for periodontal bone tissue regeneration.

摘要

生物活性纳米硅酸盐由于其内在的功能特性,如先进的生化和生物物理线索,是新兴的下一代生物材料。最近的研究表明,氟离子对干细胞具有有趣的剂量依赖性效应。尽管氟离子和纳米硅酸盐具有有趣的特性,但目前尚无关于掺氟纳米硅酸盐对干细胞影响的报道。我们系统地评估了氟纳米硅酸盐片(NS+F)与人类牙囊干细胞(hDFSCs)的相互作用,以研究其细胞毒性、细胞转运(内化)和与已报道的无氟纳米硅酸盐片(NS-F)相比的成骨分化能力。为了了解纳米硅酸盐系统的成骨诱导和骨传导特性,将纳米硅酸盐处理的 hDFSCs 在三种不同的培养基中培养,即正常生长培养基、骨传导培养基和诱导成骨培养基,培养时间长达 21 天。与 NS-F 处理的细胞相比,NS+F 处理的干细胞表现出更高的碱性磷酸酶活性、骨桥蛋白水平和明显的茜素红染色。这项研究强调了具有氟添加剂的颗粒(NS+F)有助于增强 hDFSCs 的成骨分化能力,因此是牙周骨组织再生的潜在纳米生物材料。

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