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DNA content and alkaline phosphatase expression in cells of different gingival overgrowths.

机译:不同牙龈过度生长细胞中的DNA含量和碱性磷酸酶表达。

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摘要

The present study compared the alkaline phosphatase (ALPase) expression and DNA content at specific periods in cultured cells derived from non-inflamed enlarged gingivae of idiopathic gingivofibromatosis (IGF) and phenytoin-induced hyperplasia (PHG). Cultured cells from healthy gingiva or periodontal ligament (PDL) were used as controls. The DNA assay, ALPase assay and cytochemical staining for ALPase in cultured cells were performed at four, seven, and nine days. The presence of intense ALPase activity was a prominent feature in cultured IGF cells, whereas very low ALPase activity was detected in PHG cells. The cell lines tested showed no significant differences in DNA content. The expression of ALPase in these cells was population density-dependent. The observation that cells isolated from both types of gingival overgrowth exhibited a different ALPase profile at variance with normal gingival fibroblasts suggested that a distinct pathogenic mechanism may be involved in each type of gingival overgrowth.
机译:本研究将培养细胞的特定时期与衍生自发炎的特发性牙龈作用(IGF)和苯妥林诱导的增生(PHG)的培养细胞的特定时期的碱性磷酸酶(ALPase)表达和DNA含量与培养的细胞中的特定时期进行比较。使用来自健康牙龈或牙周韧带(PDL)的培养细胞作为对照。在四个,七个和九天进行培养细胞中ALP酶的DNA测定,ALPase测定和细胞化学染色。强烈Alpase活性的存在是培养的IGF细胞中的突出特征,而在PHG细胞中检测到非常低的ALPase活性。测试的细胞系显示DNA含量没有显着差异。在这些细胞中的ALPase表达是依赖于群体密度的。观察到从两种类型的牙龈过度生长分离的细胞在常规牙龈细胞的方差上表现出不同的ALPase曲线,表明一种不同的致病机制可以参与每种类型的牙龈过度生长。

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