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垂体前叶细胞外钙的细胞类型特异性信使功能。

Cell-type specific messenger functions of extracellular calcium in the anterior pituitary.

作者信息

Zivadinovic Dragoslava, Tomić Melanija, Yuan Davy, Stojilkovic Stanko S

机构信息

Endocrinology and Reproduction Research Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-4510, USA.

出版信息

Endocrinology. 2002 Feb;143(2):445-55. doi: 10.1210/endo.143.2.8637.

Abstract

Calcium can serve not only as an intracellular messenger, but also as an extracellular messenger controlling the gating properties of plasma membrane channels and acting as an agonist for G protein-coupled Ca(2+)-sensing receptors. Here we studied the potential extracellular messenger functions of this ion in anterior pituitary cells. Depletion and repletion of the extracellular Ca(2+) concentration ([Ca(2+)]e) induced transient elevations in the intracellular Ca(2+) concentration ([Ca(2+)]i), and elevations in [Ca(2+)]e above physiological levels decreased [Ca(2+)]i in somatotrophs and lactotrophs, but not in gonadotrophs. The amplitudes and duration of [Ca(2+)]i responses depended on the [Ca(2+)]e and its rate of change, which resulted exclusively from modulation of spontaneous voltage-gated Ca(2+) influx. Changes in [Ca(2+)]e also affected GH and PRL secretion. The PRL secretory profiles paralleled the [Ca(2+)]i profiles in lactotrophs, whereas GH secretion was also stimulated by [Ca(2+)]e independently of the status of voltage-gated Ca(2+) influx. [Ca(2+)]e modulated GH secretion in a dose-dependent manner, with EC(50) values of 0.75 and 2.25 mM and minimum secretion at about 1.5 mM. In a parallel experiment, cAMP accumulation progressively increased with elevation of [Ca(2+)]e, whereas inositol phosphate levels were not affected. These results indicate the cell type-specific role of [Ca(2+)]e in the control of Ca(2+) signaling and secretion.

摘要

钙不仅可以作为细胞内信使,还可以作为细胞外信使,控制质膜通道的门控特性,并作为G蛋白偶联的Ca(2+) 传感受体的激动剂。在这里,我们研究了这种离子在前脑垂体细胞中的潜在细胞外信使功能。细胞外Ca(2+) 浓度([Ca(2+)]e)的耗尽和补充会引起细胞内Ca(2+) 浓度([Ca(2+)]i)的短暂升高,而[Ca(2+)]e升高至生理水平以上会使生长激素细胞和催乳素细胞中的[Ca(2+)]i降低,但对促性腺激素细胞没有影响。[Ca(2+)]i反应的幅度和持续时间取决于[Ca(2+)]e及其变化率,这完全是由自发电压门控Ca(2+) 内流的调节引起的。[Ca(2+)]e的变化也会影响生长激素(GH)和催乳素(PRL)的分泌。催乳素的分泌模式与催乳素细胞中的[Ca(2+)]i模式平行,而生长激素的分泌也受到[Ca(2+)]e的刺激,与电压门控Ca(2+) 内流的状态无关。[Ca(2+)]e以剂量依赖的方式调节生长激素的分泌,半数有效浓度(EC(50))值为0.75和2.25 mM,在约1.5 mM时分泌最少。在一项平行实验中,环磷酸腺苷(cAMP)的积累随着[Ca(2+)]e的升高而逐渐增加,而肌醇磷酸水平不受影响。这些结果表明[Ca(2+)]e在Ca(2+) 信号传导和分泌控制中具有细胞类型特异性作用。

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