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氟化钠对培养的人口腔角质形成细胞中DNA非定规合成的诱导作用。

Induction of unscheduled DNA synthesis in cultured human oral keratinocytes by sodium fluoride.

作者信息

Tsutsui T, Ide K, Maizumi H

出版信息

Mutat Res. 1984 May;140(1):43-8. doi: 10.1016/0165-7992(84)90069-1.

Abstract

The effect of treatment of cultured human oral keratinocytes with sodium fluoride (NaF) has been investigated with respect to induction of unscheduled DNA synthesis (UDS). Oral keratinocytes were isolated from excised buccal mucosa of normal individuals by trypsinization at 4 degrees C overnight, followed by separation of the epithelium of mucosa from lamina propria mucosae with forceps. Isolated cells were cultured in vitro and all experiments were performed with secondary cultures. For detection of UDS, the keratinocytes were cultivated with medium containing 1% fetal calf serum (FCS) for 2 days and then treated with 100-300 micrograms/ml NaF for 4 h in medium containing 1% FCS and 10 mM hydroxyurea (1% FCS-HU medium). Following treatment with NaF, UDS was measured by direct scintillation counting of [3H]thymidine incorporated into DNA of the cells in 1% FCS-HU medium. Significant levels of UDS were induced in a dose-related fashion by NaF treatment. The results suggest that NaF causes DNA damage in cultured human oral keratinocytes.

摘要

关于氟化钠(NaF)处理培养的人口腔角质形成细胞对诱导非预定DNA合成(UDS)的影响已进行了研究。通过在4℃下用胰蛋白酶消化过夜,从正常个体切除的颊粘膜中分离口腔角质形成细胞,然后用镊子将粘膜上皮与粘膜固有层分离。分离的细胞在体外培养,所有实验均使用传代培养物进行。为了检测UDS,将角质形成细胞在含有1%胎牛血清(FCS)的培养基中培养2天,然后在含有1%FCS和10mM羟基脲的培养基(1%FCS-HU培养基)中用100-300μg/ml NaF处理4小时。用NaF处理后,通过直接闪烁计数掺入1%FCS-HU培养基中细胞DNA的[3H]胸腺嘧啶核苷来测量UDS。NaF处理以剂量相关方式诱导了显著水平的UDS。结果表明,NaF在培养的人口腔角质形成细胞中引起DNA损伤。

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