Division of Endocrinology and Metabolism (B.K.M., J.-C.C., I.S., A.K.W., A.K., S.O.-L., J.M.Z.), Department of Internal Medicine; Division of Hypothalamic research (B.K.M., J.-C.C., L.K., I.S., A.K.W., A.K., S.O.-L., J.J.R., J.M.Z.), Department of Internal Medicine; and Departments of Psychiatry (B.K.M., J.-C.C., I.S., A.K.W., A.K., S.O.-L., J.M.Z.) and Physiology (L.K., J.J.R.), University of Texas Southwestern Medical Center, Dallas, Texas 75390.
Endocrinology. 2014 Jan;155(1):98-107. doi: 10.1210/en.2013-1691. Epub 2013 Dec 20.
Ghrelin is an orexigenic hormone secreted principally from a distinct population of gastric endocrine cells. Molecular mechanisms regulating ghrelin secretion are mostly unknown. Recently, norepinephrine (NE) was shown to enhance ghrelin release by binding to β1-adrenergic receptors on ghrelin cells. Here, we use an immortalized stomach-derived ghrelin cell line to further characterize the intracellular signaling pathways involved in NE-induced ghrelin secretion, with a focus on the roles of Ca(2+) and cAMP. Several voltage-gated Ca(2+) channel (VGCC) family members were found by quantitative PCR to be expressed by ghrelin cells. Nifedipine, a selective L-type VGCC blocker, suppressed both basal and NE-stimulated ghrelin secretion. NE induced elevation of cytosolic Ca(2+) levels both in the presence and absence of extracellular Ca(2+). Ca(2+)-sensing synaptotagmins Syt7 and Syt9 were also highly expressed in ghrelin cell lines, suggesting that they too help mediate ghrelin secretion. Raising cAMP with the phosphodiesterase inhibitor 3-isobutyl-1-methylxanthine also stimulated ghrelin secretion, although such a cAMP-mediated effect likely does not involve protein kinase A, given the absence of a modulatory response to a highly selective protein kinase A inhibitor. However, pharmacological inhibition of another target of cAMP, exchange protein-activated by cAMP (EPAC), did attenuate both basal and NE-induced ghrelin secretion, whereas an EPAC agonist enhanced basal ghrelin secretion. We conclude that constitutive ghrelin secretion is primarily regulated by Ca(2+) influx through L-type VGCCs and that NE stimulates ghrelin secretion predominantly through release of intracellular Ca(2+). Furthermore, cAMP and its downstream activation of EPAC are required for the normal ghrelin secretory response to NE.
胃饥饿素是一种主要由胃内分泌细胞分泌的食欲激素。调节胃饥饿素分泌的分子机制大多未知。最近,去甲肾上腺素(NE)通过与胃饥饿素细胞上的β1-肾上腺素能受体结合,被证明可以增强胃饥饿素的释放。在这里,我们使用一种永生化的胃源性胃饥饿素细胞系来进一步描述参与 NE 诱导的胃饥饿素分泌的细胞内信号通路,重点是 Ca(2+)和 cAMP 的作用。通过定量 PCR 发现,几种电压门控 Ca(2+)通道(VGCC)家族成员在胃饥饿素细胞中表达。尼非地平是一种选择性 L 型 VGCC 阻断剂,可抑制基础和 NE 刺激的胃饥饿素分泌。NE 诱导的细胞浆 Ca(2+)水平升高,无论是否存在细胞外 Ca(2+)。Ca(2+)敏感的突触结合蛋白 Syt7 和 Syt9 在胃饥饿素细胞系中也高度表达,表明它们也有助于介导胃饥饿素分泌。用磷酸二酯酶抑制剂 3-异丁基-1-甲基黄嘌呤升高 cAMP 也刺激胃饥饿素分泌,尽管这种 cAMP 介导的效应可能不涉及蛋白激酶 A,因为对高度选择性蛋白激酶 A 抑制剂没有调节反应。然而,另一种 cAMP 的靶标,cAMP 激活的交换蛋白(EPAC)的药理学抑制作用减弱了基础和 NE 诱导的胃饥饿素分泌,而 EPAC 激动剂增强了基础胃饥饿素分泌。我们得出结论,基础胃饥饿素分泌主要受 L 型 VGCC 介导的 Ca(2+)内流调节,而 NE 主要通过释放细胞内 Ca(2+)刺激胃饥饿素分泌。此外,cAMP 及其下游 EPAC 的激活对于正常的胃饥饿素对 NE 的分泌反应是必需的。