Harvey B J, Higgins M
Wellcome Trust Cellular Physiology Research Unit, Department of Physiology, University College, Cork, Ireland.
Kidney Int. 2000 Apr;57(4):1395-403. doi: 10.1046/j.1523-1755.2000.00981.x.
Aldosterone at physiological levels induces rapid (<5 min) increases in intracellular protein kinase C (PKC) activity and a rise in calcium and pH in mineralocorticoid hormone target epithelia, such as distal colon and sweat gland. The end targets of these rapid responses in epithelia are Na+/H+ exchange and K+ channels.
The mouse cortical collecting duct (CCD) M-1 cell line was grown to confluency and loaded with Fura-2 for spectrofluorescence measurements of intracellular free calcium at 37 degrees C bathed in Krebs solution.
Aldosterone (1 nmol/L) produced a rapid, transient peak increase in [Ca2+]i in M-1 cells. This effect was abolished upon removal of extracellular Ca2+, but was unaffected by pretreatment with spironolactone (10 micromol/L) or actinomycin D (10 micromol/L). However, pretreatment with the specific PKC inhibitor chelerythrine chloride (1 micromol/L) prevented the aldosterone-induced rise in [Ca2+]i. Dexamethasone, at a concentration 10,000-fold higher than aldosterone (10 micromol/L), also produced a transient increase in [Ca2+]i, but this response was significantly smaller than that of aldosterone. In contrast, hydrocortisone had no effect on [Ca2+]i at either nmol/L or micromol/L concentrations. Both of the sex steroids, 17beta-estradiol (10 nmol/L) and progesterone (10 nmol/L), induced protein kinase C-dependent increases in [Ca2+]i.
Aldosterone and sex steroid hormones activate intracellular calcium signaling in CCD cells via a nongenomic PKC-dependent pathway, which may have important implications for renal transport.
生理水平的醛固酮可在盐皮质激素靶上皮细胞(如远端结肠和汗腺)中诱导细胞内蛋白激酶C(PKC)活性迅速(<5分钟)增加以及钙和pH值升高。这些上皮细胞中这些快速反应的最终靶点是Na+/H+交换和钾通道。
将小鼠皮质集合管(CCD)M-1细胞系培养至汇合,并加载Fura-2,以便在37℃下于Krebs溶液中进行细胞内游离钙的光谱荧光测量。
醛固酮(1 nmol/L)使M-1细胞内的[Ca2+]i迅速出现短暂的峰值增加。去除细胞外钙后,这种效应消失,但不受螺内酯(10 μmol/L)或放线菌素D(10 μmol/L)预处理的影响。然而,用特异性PKC抑制剂氯化白屈菜红碱(1 μmol/L)预处理可阻止醛固酮诱导的[Ca2+]i升高。地塞米松浓度比醛固酮高10000倍(10 μmol/L)时,也会使[Ca2+]i出现短暂增加,但这种反应明显小于醛固酮引起的反应。相比之下,氢化可的松在nmol/L或μmol/L浓度下对[Ca2+]i均无影响。两种性类固醇激素,17β-雌二醇(10 nmol/L)和孕酮(10 nmol/L),均可诱导PKC依赖性的[Ca2+]i增加。
醛固酮和性类固醇激素通过非基因组PKC依赖性途径激活CCD细胞内的钙信号传导,这可能对肾脏转运具有重要意义。