Lehenkari P P, Laitala-Leinonen T, Linna T J, Väänänen H K
Department of Anatomy, University of Oulu, Finland.
Biochem Biophys Res Commun. 1997 Jun 27;235(3):838-44. doi: 10.1006/bbrc.1997.6894.
The present study was performed to clarify the role of vacuolar H+-ATPase in the regulation of the intracellular pH (pHi) in osteoclasts. Bafilomycin A1 or amiloride were added to rat osteoclast cultures to block the H+-ATPases and Na+/H+-exchangers, respectively. Addition of 10(-8) M bafilomycin A1 to osteoclasts cultured on bone induced a rapid decrease of the pHi, while addition of amiloride had only a minor effect. The response to bafilomycin A1 appeared simultaneously with resorption activity and was abolished when resorption was inhibited by calcitonin. Osteoclasts on bone recovered from acid loading caused by propionate in the presence of amiloride, while bafilomycin A1 inhibited this recovery almost completely. The pHi of osteoclasts cultured on glass responded to the addition of amiloride, but was not effected by even high concentrations of bafilomycin A1. In contrast, as little as 10(-10) M bafilomycin A1 caused accumulation of large vesicles in the cytoplasm.
本研究旨在阐明液泡H⁺-ATP酶在破骨细胞内pH(pHi)调节中的作用。分别向大鼠破骨细胞培养物中添加巴弗洛霉素A1或阿米洛利,以分别阻断H⁺-ATP酶和Na⁺/H⁺交换体。向在骨上培养的破骨细胞中添加10⁻⁸M巴弗洛霉素A1会导致pHi迅速下降,而添加阿米洛利的影响较小。对巴弗洛霉素A1的反应与吸收活性同时出现,当降钙素抑制吸收时该反应消失。在阿米洛利存在的情况下,骨上的破骨细胞从丙酸盐引起的酸负荷中恢复,而巴弗洛霉素A1几乎完全抑制了这种恢复。在玻璃上培养的破骨细胞的pHi对阿米洛利的添加有反应,但即使是高浓度的巴弗洛霉素A1也没有影响。相反,低至10⁻¹⁰M的巴弗洛霉素A1会导致细胞质中出现大量囊泡积聚。