Anderson R E, Jee W S, Woodbury D M
Calcif Tissue Int. 1985 Dec;37(6):646-50. doi: 10.1007/BF02554924.
Changes in the acidity of osteoclasts were evaluated by direct measurement of the fluorescent intensity of osteoclasts exposed to acridine orange, a fluorescent weak base which becomes concentrated in acid-containing subcellular compartments. Parathyroid hormone (PTH) produced dose-dependent increases in fluorescent intensity; maximal increases in intensity occurred at doses between 3 and 10 micrograms PTH/ml of culture medium. Acetazolamide, a potent inhibitor of carbonic anhydrase, inhibited the increase in fluorescence induced by PTH, but this drug was less effective in reducing fluorescence in maximally than in submaximally stimulated osteoclasts, indicating that either more enzyme or more resistant enzyme was present in the PTH-stimulated cells. Because increased fluorescence of acridine orange is a sign of greater acidity, these results suggest that (1) PTH stimulates the acidity of osteoclasts, (2) carbonic anhydrase activity is necessary for maximum acidity, and (3) carbonic anhydrase is activated by PTH.
通过直接测量暴露于吖啶橙(一种荧光弱碱,可在含酸的亚细胞区室中浓缩)的破骨细胞的荧光强度,评估破骨细胞酸度的变化。甲状旁腺激素(PTH)使荧光强度呈剂量依赖性增加;在培养基中PTH浓度为3至10微克/毫升时,荧光强度出现最大增加。碳酸酐酶的强效抑制剂乙酰唑胺抑制了PTH诱导的荧光增加,但该药物在最大程度上降低荧光方面,对受最大刺激的破骨细胞的效果比对受次最大刺激的破骨细胞的效果要差,这表明在PTH刺激的细胞中,要么存在更多的酶,要么存在更具抗性的酶。由于吖啶橙荧光增强是酸度增加的标志,这些结果表明:(1)PTH刺激破骨细胞的酸度;(2)碳酸酐酶活性对于最大酸度是必需的;(3)碳酸酐酶被PTH激活。