Lyaruu D M, Wöltgens J H, Bervoets T J
Department of Oral Cell Biology, School of Dentistry, Vrije Universiteit, Amsterdam, The Netherlands.
Arch Oral Biol. 1987;32(6):429-32. doi: 10.1016/0003-9969(87)90078-1.
In culture, 1-p-bromotetramisole (pBTM), a specific inhibitor of alkaline phosphatase, significantly inhibited the formation of trichloroacetic acid (TCA)-insoluble [32P]-phosphate from inorganic [32P]-phosphate in the proliferating non-mineralizing second (M2) maxillary molar germs but had no effect in the actively mineralizing first (M1) germs. Addition of 10(-5) M inorganic pyrophosphate in the culture medium with a [32P]-phosphate label increased the inhibition of the formation of TCA-insoluble [32P]-phosphate in the M2. pBTM almost completely inhibited the formation of TCA-insoluble [32P]-phosphate from inorganic [32P]-pyrophosphate in the non-mineralizing M2. In the actively mineralizing M1, the compound significantly inhibited but did not abolish the formation of TCA-insoluble phosphate. These results confirm earlier biochemical findings that alkaline phosphatase possesses a pyrophosphatase activity probably related to the turnover of phosphorylated macromolecules necessary for cell differentiation and proliferation.
在培养过程中,碱性磷酸酶的特异性抑制剂1 - 对溴四咪唑(pBTM)显著抑制了增殖但未矿化的上颌第二磨牙(M2)牙胚中无机[32P] - 磷酸盐形成三氯乙酸(TCA)不溶性[32P] - 磷酸盐,但对正在积极矿化的第一磨牙(M1)牙胚没有影响。在含有[32P] - 磷酸盐标记的培养基中添加10^(-5) M无机焦磷酸盐可增强对M2中TCA不溶性[32P] - 磷酸盐形成的抑制作用。pBTM几乎完全抑制了未矿化的M2中无机[32P] - 焦磷酸盐形成TCA不溶性[32P] - 磷酸盐。在正在积极矿化的M1中,该化合物显著抑制但并未消除TCA不溶性磷酸盐的形成。这些结果证实了早期的生化研究发现,即碱性磷酸酶具有焦磷酸酶活性,这可能与细胞分化和增殖所需的磷酸化大分子的周转有关。