Hao J, Wang P, Shi J
School of Stomatology, Fourth Military Medical University, Xi'an 710032.
Zhonghua Kou Qiang Yi Xue Za Zhi. 1999 Jul;34(4):239-41.
To evaluate the effects of human basic fibroblast growth factor (hbFGF) on proliferation and differentiation of human dental pulp cells in vitro.
The syntheses of DNA, collagen, fibronection (FN), alkaline phosphatase (ALP) and bone morphogenetic protein (BMP), and the expression of agglutinin were measured with imagine processing and analysis system.
hbFGF at concentration of 1-10 micrograms/L stimulated the cell proliferation measured by MTT colorimetric assay, and promoted incorporation of 3H-thymidine at 1-100 micrograms/L. The expression of type I collagen, FN, Con A receptor, and ALP significantly increased at hbFGF concentration of 10-1,000 micrograms/L, but the expression of type III collagen and WGA receptor markedly decreased at the same concentration. There was no significant difference in expression of BMP.
bFGF has the capability to promote the differentiation of dental pulp cells to odontoblasts in culture.
评估人碱性成纤维细胞生长因子(hbFGF)对体外培养的人牙髓细胞增殖和分化的影响。
采用图像分析系统检测DNA、胶原蛋白、纤连蛋白(FN)、碱性磷酸酶(ALP)和骨形态发生蛋白(BMP)的合成以及凝集素的表达。
浓度为1-10微克/升的hbFGF通过MTT比色法刺激细胞增殖,并在1-100微克/升促进3H-胸腺嘧啶核苷掺入。在hbFGF浓度为10-1000微克/升时,I型胶原蛋白、FN、伴刀豆球蛋白A受体和ALP的表达显著增加,但在相同浓度下III型胶原蛋白和麦胚凝集素受体的表达明显降低。BMP的表达无显著差异。
bFGF有能力促进培养的牙髓细胞向成牙本质细胞分化。