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Mesenchymal Stem Cells Derived from Healthy and Diseased Human Gingiva Support Osteogenesis on Electrospun Polycaprolactone Scaffolds

机译:从健康和患病的人牙龈衍生的间充质干细胞支持静电纺丝聚己内酯支架上的成骨作用。

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Periodontitis is a chronic inflammatory disease affecting almost half of the adult US population. Gingiva is an integral part of the periodontium and has recently been identified as a source of adult gingiva-derived mesenchymal stem cells (GMSCs). Given the prevalence of periodontitis, the purpose of this study is to evaluate differences between GMSCs derived from healthy and diseased gingival tissues and explore their potential in bone engineering. Primary clonal cell lines were established from harvested healthy and diseased gingival and characterized for expression of known stem-cell markers and multi-lineage differentiation potential. Finally, they were cultured on electrospun polycaprolactone (PCL) scaffolds and evaluated for attachment, proliferation, and differentiation. Flow cytometry demonstrated cells isolated from healthy and diseased gingiva met the criteria defining mesenchymal stem cells (MSCs). However, GMSCs from diseased tissue showed decreased colony-forming unit efficiency, decreased alkaline phosphatase activity, weaker osteoblast mineralization, and greater propensity to differentiate into adipocytes than their healthy counterparts. When cultured on electrospun PCL scaffolds, GMSCs from both sources showed robust attachment and proliferation over a 7-day period; they exhibited high mineralization as well as strong expression of alkaline phosphatase. Our results show preservation of ‘stemness’ and osteogenic potential of GMSC even in the presence of disease, opening up the possibility of using routinely discarded, diseased gingival tissue as an alternate source of adult MSCs.
机译:牙周炎是一种慢性炎性疾病,几乎影响了美国成年人口的一半。牙龈是牙周组织不可或缺的一部分,最近被确定为成年牙龈来源的间充质干细胞(GMSC)的来源。考虑到牙周炎的流行,本研究的目的是评估源自健康和患病牙龈组织的GMSC之间的差异,并探讨其在骨工程中的潜力。从收获的健康和患病的牙龈中建立原代克隆细胞系,并对其表达进行表征,以表达已知的干细胞标记物和多系分化潜能。最后,将它们在静电纺丝聚己内酯(PCL)支架上培养,并评估其附着,增殖和分化。流式细胞术表明,从健康和患病的牙龈分离的细胞符合定义间充质干细胞(MSCs)的标准。但是,来自患病组织的GMSC表现出降低的菌落形成单位效率,降低的碱性磷酸酶活性,较弱的成骨细胞矿化以及比其健康的对应物更大的分化成脂肪细胞的倾向。当在静电纺丝PCL支架上培养时,两种来源的GMSC在7天的时间内都显示出牢固的附着和增殖。它们显示出高矿化度以及碱性磷酸酶的强表达。我们的结果表明,即使在存在疾病的情况下,GMSC的“干性”和成骨潜能也得以保留,从而开辟了将常规丢弃的,患病的牙龈组织用作成人MSC的替代来源的可能性。

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