Kakinuma Y, Sakamaki Y, Ito K, Cragoe E J, Igarashi K
Faculty of Pharmaceutical Sciences, Chiba University, Japan.
Arch Biochem Biophys. 1987 Nov 15;259(1):171-8. doi: 10.1016/0003-9861(87)90483-8.
The relationship among activation of the Na+/H+ antiporter, ornithine decarboxylase, and DNA synthesis was examined with bovine small lymphocytes stimulated by concanavalin A (Con A). The Na+/H+ antiport activity was activated immediately after addition of concanavalin A; the maximum was reached 1 h after Con A addition and the activation continued at least 6 h. With increasing concanavalin A concentrations, the activities of the Na+/H+ antiporter, ornithine decarboxylase, and DNA synthesis increased in a parallel manner. In the presence of HCO3- in the medium, the internal alkalinization of lymphocytes was not induced by Con A. Ornithine decarboxylase and DNA synthetic activities were not inhibited by 5-(N-ethyl-N-isopropyl) amiloride (EIPA), a specific inhibitor of the Na+/H+ antiporter. In contrast, in the absence of HCO3- in the medium, the internal pH was alkalinized approximately 0.06 pH units by Con A. EIPA did inhibit the alkalinization of the internal pH or DNA synthesis significantly. Ornithine decarboxylase activity was not inhibited by EIPA. These results indicate that the activation of a Na+/H+ antiporter is not a trigger for cell proliferation, but its activation is important probably through the maintenance of the internal pH optimum, especially in HCO3(-)-free medium.
用伴刀豆球蛋白A(Con A)刺激牛小淋巴细胞,研究了Na⁺/H⁺逆向转运蛋白激活、鸟氨酸脱羧酶和DNA合成之间的关系。加入伴刀豆球蛋白A后,Na⁺/H⁺逆向转运活性立即被激活;在加入Con A后1小时达到最大值,且激活至少持续6小时。随着伴刀豆球蛋白A浓度的增加,Na⁺/H⁺逆向转运蛋白、鸟氨酸脱羧酶的活性和DNA合成以平行方式增加。在培养基中存在HCO₃⁻的情况下,Con A不会诱导淋巴细胞的细胞内碱化。5-(N-乙基-N-异丙基)氨氯吡脒(EIPA)是Na⁺/H⁺逆向转运蛋白的特异性抑制剂,它不会抑制鸟氨酸脱羧酶和DNA合成活性。相反,在培养基中不存在HCO₃⁻的情况下,Con A可使细胞内pH值碱化约0.06个pH单位。EIPA确实能显著抑制细胞内pH值的碱化或DNA合成。鸟氨酸脱羧酶活性不受EIPA抑制。这些结果表明,Na⁺/H⁺逆向转运蛋白的激活不是细胞增殖的触发因素,但其激活可能通过维持细胞内最佳pH值而很重要,特别是在无HCO₃⁻的培养基中。