human dental pulp cell

基本解釋

Conclusion The expression of TIMP-1, -2 in human dental pulp cell and tissue is detected, and this provides the basis for further studying on the mechanism of TIMP in dental pulp.
結(jié)論TIMP 1、 2在人牙髓成纖維細(xì)胞及牙髓組織均有表達(dá)，為進(jìn)一步研究TIMP在牙髓組織中的作用機(jī)理提供實(shí)驗(yàn)依據(jù)。
Methods:The culture supernatant of monocytes stimulated with Fn LPS was applied to human dental pulp cell in vitro, and activity of ALP in human dental pulp fibroblast was monitored by OD test.
方法：采用經(jīng)具核梭桿菌LPS刺激的單核細(xì)胞培養(yǎng)上清作用于體外培養(yǎng)的人牙髓細(xì)胞，通過OD值測定，觀察單核細(xì)胞培養(yǎng)上清對人牙髓成纖維細(xì)胞堿性磷酸酶（ALP）活性的影響。
To evaluate the cytotoxicity of dental resin monomer exposed to human pulp cells and to investigate the sensitivity of different cell lines to the monomer.
目的：評價(jià)復(fù)合樹脂單體對人牙髓的毒性作用，探討不同細(xì)胞系對檢測敏感性的影響。

牙髓細(xì)胞
Objective: Isolate and cultivate human pulp cells to study their biological Characterization. This study assess Capacitively coupled electric fields as a new type of electrical stimulation to induce the proliferation of the human dental pulp cell.
目的分離培養(yǎng)人牙髓細(xì)胞,探討其基本的增殖、分化等生物學(xué)特性,通過利用電容耦合電刺激牙髓細(xì)胞,研究其對體外培養(yǎng)人牙髓細(xì)胞增殖的影響,以探索利用微電流環(huán)境在牙組織工程中應(yīng)用的前景。