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低浓度氟对人牙髓细胞体外增殖及碱性磷酸酶活性的刺激作用。

Stimulation by low concentrations of fluoride of the proliferation and alkaline phosphatase activity of human dental pulp cells in vitro.

作者信息

Nakade O, Koyama H, Arai J, Ariji H, Takada J, Kaku T

机构信息

Department of Oral Pathology, School of Dentistry, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Japan.

出版信息

Arch Oral Biol. 1999 Jan;44(1):89-92. doi: 10.1016/s0003-9969(98)00099-5.

Abstract

Fluoride has been used for decades, either systemically or topically, to prevent dental caries. The purpose of this study was to clarify the effects of low concentrations of fluoride on proliferation, differentiation and extracellular-matrix synthesis in normal human dental pulp cells (DP-1 and DP-2) in vitro. The effects were compared with those on a human osteoblastic osteosarcoma cell line, TE-85. Fluoride at micromolar concentrations significantly and dose-dependently stimulated [3H]thymidine incorporation into DNA in DP-1, DP-2 and TE-85 cells, with optimal effects around 50 microM, by 127 +/- 7%, 124 +/- 0.6% and 152 +/- 13.4%, respectively. To assess the potential influence of fluoride on cell differentiation, the effects of mitogenic concentrations on alkaline phosphatase activity were measured. Fluoride significantly increased the enzyme's activity in DP-1 and TE-85 by 177 +/- 12% and 144 +/- 12.3%. To evaluate the effect on extracellular-matrix synthesis, the synthesis of type I collagen was indirectly determined by an assay of procollagen type I c-peptide production. Fluoride significantly increased that production by 150 +/- 8.7% in TE-85, but not in either DP-1 or DP-2. These observations suggest that fluoride, if used at low concentrations, could be a useful therapeutic agent where increased regeneration of dentine is desired, such as after pulp amputation, by stimulating the proliferation and differentiation of the dental pulp cells.

摘要

几十年来,氟化物一直被用于全身或局部预防龋齿。本研究的目的是阐明低浓度氟化物对正常人牙髓细胞(DP - 1和DP - 2)体外增殖、分化和细胞外基质合成的影响。并将这些影响与对人成骨骨肉瘤细胞系TE - 85的影响进行比较。微摩尔浓度的氟化物能显著且剂量依赖性地刺激DP - 1、DP - 2和TE - 85细胞将[³H]胸苷掺入DNA,最佳效应浓度约为50微摩尔,分别使掺入量增加127±7%、124±0.6%和152±13.4%。为评估氟化物对细胞分化的潜在影响,测量了促有丝分裂浓度的氟化物对碱性磷酸酶活性的影响。氟化物使DP - 1和TE - 85中的该酶活性分别显著增加177±12%和144±12.3%。为评估对细胞外基质合成的影响,通过检测I型前胶原c肽的产生间接测定I型胶原的合成。氟化物使TE - 85中的该产物显著增加150±8.7%,但在DP - 1或DP - 2中均未增加。这些观察结果表明,低浓度使用时,氟化物可能是一种有用的治疗剂,通过刺激牙髓细胞的增殖和分化,在需要增加牙本质再生的情况下,如牙髓切断术后发挥作用。

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