Holl R W, Thorner M O, Leong D A
Department of Internal Medicine, University of Virginia Medical Center, Charlottesville 22908.
Am J Physiol. 1989 Mar;256(3 Pt 1):E375-9. doi: 10.1152/ajpendo.1989.256.3.E375.
Digital imaging microscopy using the calcium-sensitive indicator probe fura-2 was combined with a reverse hemolytic plaque assay (RHPA) for growth hormone (GH) secretion. This technique allows dynamic measurements of the cytosolic free calcium concentration ([Ca2+]i) in individual pituitary somatotropes. Stimulation by growth hormone-releasing factor (GRF) increases, whereas somatostatin (SRIF) reduces [Ca2+]i in this cell type. [Ca2+]i increased in somatotropes when the cellular content of adenosine 3',5'-cyclic monophosphate (cAMP) was elevated by 1) activating cellular adenylate cyclase with forskolin (5 microM) and 2) treatment with the cAMP-analogues dibutyryl-cAMP (1 mM) or 8-bromo-cAMP (5 mM). The forskolin-induced calcium rise was abolished in the absence of extracellular calcium. This indicates that cAMP increases the influx of calcium into the cytosol and thereby stimulates hormone release. When forskolin was given in combination with SRIF (10 nM), [Ca2+]i decreased to the same level reached with SRIF treatment alone, indicating a site of action distal to the generation of cAMP. Activating protein kinase C with the phorbol ester 12,13-phorbol dibutyrate (PDB; 100 nM) increased [Ca2+]i as well. Again, this effect was dependent on extracellular calcium and blocked when PDB and SRIF were applied simultaneously. Combined stimulation with GRF plus PDB did not augment the response of [Ca2+]i over GRF treatment alone.
使用钙敏感指示剂探针fura-2的数字成像显微镜与用于生长激素(GH)分泌的反向溶血空斑试验(RHPA)相结合。该技术可动态测量单个垂体生长激素细胞中的胞质游离钙浓度([Ca2+]i)。生长激素释放因子(GRF)刺激可使[Ca2+]i升高,而生长抑素(SRIF)则使其降低。当通过以下方式升高细胞内3',5'-环磷酸腺苷(cAMP)的含量时,生长激素细胞中的[Ca2+]i会升高:1)用福司可林(5 microM)激活细胞腺苷酸环化酶;2)用cAMP类似物二丁酰-cAMP(1 mM)或8-溴-cAMP(5 mM)处理。在没有细胞外钙的情况下,福司可林诱导的钙升高被消除。这表明cAMP增加了钙流入胞质溶胶,从而刺激激素释放。当福司可林与SRIF(10 nM)联合使用时,[Ca2+]i降至单独使用SRIF处理时达到的相同水平,表明作用位点在cAMP生成的远端。用佛波酯12,13-二丁酰佛波醇(PDB;100 nM)激活蛋白激酶C也会增加[Ca2+]i。同样,这种作用依赖于细胞外钙,当同时应用PDB和SRIF时会被阻断。GRF加PDB的联合刺激并没有比单独使用GRF治疗增强[Ca2+]i的反应。