Hruska K A, Goligorsky M, Scoble J, Tsutsumi M, Westbrook S, Moskowitz D
Am J Physiol. 1986 Aug;251(2 Pt 2):F188-98. doi: 10.1152/ajprenal.1986.251.2.F188.
The effects of parathyroid hormone on the cytoplasmic Ca2+ concentration of canine renal proximal tubule cells grown in primary culture were determined using the fluorescent Ca2+ indicator quin 2. The cultured cells exhibited responses to hormones, enzyme activities, transport functions, and morphology characteristic of the proximal convoluted tubule. Parathyroid hormone stimulated an immediate rise in cytoplasmic Ca2+, both in suspended cells and cells studied as a monolayer on Nuclepore filters. The rise in cytoplasmic Ca2+ induced by the hormone was sustained for 15-30 min, was dose dependent, and was not mimicked by cyclic AMP. Removing Ca2+ from the extracellular media markedly decreased cytoplasmic Ca2+ and abolished the effects of parathyroid hormone on cytosolic Ca2+. 8-(N,N-diethylamino)octyl-3,4,5-trimethoxybenzoate blocked the effects of the hormone on cytosolic Ca2+, but mitochondrial uncouplers failed to inhibit the effects of the hormone to increase cytoplasmic Ca2+. These studies support a role of Ca2+ in the activation of proximal renal tubule cells by parathyroid hormone.
使用荧光钙指示剂喹啉-2测定甲状旁腺激素对原代培养的犬肾近端小管细胞胞质钙离子浓度的影响。培养的细胞表现出对激素、酶活性、转运功能以及近曲小管特征性形态的反应。甲状旁腺激素可刺激悬浮细胞以及在核孔滤膜上作为单层研究的细胞的胞质钙离子立即升高。该激素诱导的胞质钙离子升高持续15 - 30分钟,呈剂量依赖性,且不被环磷酸腺苷模拟。从细胞外培养基中去除钙离子可显著降低胞质钙离子,并消除甲状旁腺激素对胞质钙离子的影响。8 -(N,N - 二乙氨基)辛基 - 3,4,5 - 三甲氧基苯甲酸可阻断该激素对胞质钙离子的影响,但线粒体解偶联剂未能抑制该激素增加胞质钙离子的作用。这些研究支持钙离子在甲状旁腺激素激活近端肾小管细胞中的作用。