Vignery A, Wang F, Ganz M B
Department of Orthopaedics and Rehabilitation, West Haven V.A. Medical Center, Yale University School of Medicine, New Haven, Connecticut 06510.
J Cell Physiol. 1991 Nov;149(2):301-6. doi: 10.1002/jcp.1041490217.
The present study was designed to investigate whether non-activated macrophages express calcitonin (CT) or calcitonin-gene-related peptide (CGRP) receptors. To this end, we first analyzed whether CT and CGRP induce a cAMP accumulation in macrophages. Macrophages were treated for 2 min with increasing concentrations of either CT or CGRP in the presence or absence of IBMX. A dose-dependent cAMP accumulation was measured in response to CGRP with a half-maximal effect attained with 1 nM CGRP. CT failed at all doses to induce an accumulation of cAMP. The effects of CT and CGRP on the activation of the Na-H exchanger were next assessed by spectrofluorometry by using the pH-sensitive dye 2,7 biscarboxyethyl-5(6)-carboxyfluorescein (BCECF). Steady-state pHi of macrophages in a 7.4, HCO3-free solution (HEPES-buffered) was 7.04 +/- 0.08 (n = 22). pHi recovery following an NH4+/NH3 acid load was inhibited by the removal of Na+ or by the addition of the amiloride analog EIPA; therefore recovery is dependent on Na-H exchange activity. CT had no effect on steady-state pHi but CGRP increased pHi in a dose-dependent fashion (10(-12) to 10(-6) M). The pHi change induced by CGRP was due to the stimulation of the Na-H exchanger as CGRP enhanced the rate of recovery (dpHi/dt) from an acid load from 45.3 to 77.2 microMs-1 (n = 8, P less than 0.002) and was completely blocked by EIPA. These data indicate that CGRP both enhances the activity of the Na-H exchanger and increases intracellular cAMP, thus demonstrating that macrophages express functional CGRP receptors.
本研究旨在调查未激活的巨噬细胞是否表达降钙素(CT)或降钙素基因相关肽(CGRP)受体。为此,我们首先分析了CT和CGRP是否能在巨噬细胞中诱导cAMP积累。在存在或不存在异丁基甲基黄嘌呤(IBMX)的情况下,用浓度递增的CT或CGRP处理巨噬细胞2分钟。在1 nM CGRP时达到半数最大效应,对CGRP的反应中检测到剂量依赖性的cAMP积累。所有剂量的CT均未能诱导cAMP积累。接下来,通过使用pH敏感染料2,7-双羧乙基-5(6)-羧基荧光素(BCECF)的荧光分光光度法评估CT和CGRP对钠氢交换体激活的影响。在无HCO3(HEPES缓冲)的7.4溶液中,巨噬细胞的稳态细胞内pH(pHi)为7.04±0.08(n = 22)。去除Na+或添加氨氯吡脒类似物EIPA可抑制NH4+/NH3酸负荷后pHi的恢复;因此,恢复依赖于钠氢交换活性。CT对稳态pHi无影响,但CGRP以剂量依赖性方式(10(-12)至10(-6) M)增加pHi。CGRP诱导的pHi变化是由于钠氢交换体的刺激,因为CGRP将酸负荷后的恢复速率(dpHi/dt)从45.3提高到77.2 μM/s(n = 8,P<0.002),并且被EIPA完全阻断。这些数据表明,CGRP既能增强钠氢交换体的活性,又能增加细胞内cAMP,从而证明巨噬细胞表达功能性CGRP受体。