Malmström K, Stange G, Murer H
Department of Physiology, University of Zurich, Switzerland.
Biochem J. 1988 Apr 1;251(1):207-13. doi: 10.1042/bj2510207.
Parathyroid hormone (PTH) increased intracellular cyclic AMP and reduces Na+/phosphate cotransport activity in OK cells [Malmström & Murer (1986) Am. J. Physiol. 251, C23-C31; Caverzasio, Rizzoli & Bonjour (1986) J. Biol. Chem. 261, 3233-3237]. It was also shown that PTH activates phosphoinositide metabolism in OK cells [Hruska, Moskowitz, Esprit, Civitelli, Westbrook & Huskey (1987) J. Clin. Invest. 79, 230-239]. In the present paper we show that tumour-promoting phorbol esters are effective in reducing Na+/phosphate cotransport. The Ca2+ ionophores A23187 and ionomycin had only a small effect on Na+/phosphate cotransport; added together, A23187 and phorbol esters showed a synergistic action. Phorbol esters and phorbol esters plus ionomycin stimulated prostaglandin synthesis as well as cyclic AMP production; acetylsalicylic acid prevented phorbol-ester-induced prostaglandin synthesis and cyclic AMP production, but had no effect on inhibition of Na+/phosphate cotransport. In suspensions of OK cells, PTH and thrombin produced a rise in intracellular Ca2+. In contrast with PTH, thrombin did not elevate cellular cyclic AMP in suspended OK cells. PTH and thrombin reduced Na+/phosphate cotransport in suspended OK cells. It is suggested that two regulatory cascades are involved in PTH action on Na+/phosphate cotransport: cyclic AMP/kinase A and Ca2+/diacylglycerol/kinase C.
甲状旁腺激素(PTH)可增加OK细胞内的环磷酸腺苷(cAMP)含量,并降低其Na⁺/磷酸盐共转运活性[马尔姆斯特伦和穆勒(1986年),《美国生理学杂志》251卷,C23 - C31页;卡韦尔扎西奥、里佐利和邦茹尔(1986年),《生物化学杂志》261卷,3233 - 3237页]。研究还表明,PTH可激活OK细胞中的磷酸肌醇代谢[赫鲁斯卡、莫斯科维茨、埃斯普里、奇维泰利、韦斯特布鲁克和赫斯基(1987年),《临床研究杂志》79卷,230 - 239页]。在本文中,我们表明促肿瘤的佛波酯可有效降低Na⁺/磷酸盐共转运。钙离子载体A23187和离子霉素对Na⁺/磷酸盐共转运的影响较小;A23187与佛波酯共同作用时表现出协同效应。佛波酯以及佛波酯加离子霉素可刺激前列腺素合成以及环磷酸腺苷的产生;乙酰水杨酸可阻止佛波酯诱导的前列腺素合成和环磷酸腺苷产生,但对抑制Na⁺/磷酸盐共转运没有作用。在OK细胞悬液中,PTH和凝血酶可使细胞内钙离子浓度升高。与PTH不同的是,凝血酶不会使悬浮的OK细胞内的环磷酸腺苷升高。PTH和凝血酶可降低悬浮OK细胞中的Na⁺/磷酸盐共转运。研究表明,PTH对Na⁺/磷酸盐共转运的作用涉及两条调节途径:环磷酸腺苷/蛋白激酶A和钙离子/二酰基甘油/蛋白激酶C。