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首页> 外文期刊>Pfluegers Archiv: European Journal of Physiology >Differential calcium responses to the pituitary adenylate cyclase-activating polypeptide (PACAP) in the five main cell types of rat anterior pituitary.
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Differential calcium responses to the pituitary adenylate cyclase-activating polypeptide (PACAP) in the five main cell types of rat anterior pituitary.

机译:大鼠垂体前五种主要细胞类型中对垂体腺苷酸环化酶激活多肽(PACAP)的钙反应差异。

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摘要

We have compared the effects of pituitary adenylate cyclase-activating polypeptide (PACAP-27) on the five main cell types of rat anterior pituitary in primary culture by monitoring changes in cytosolic Ca2+ concentration ([Ca2+]i) in single fura-2-loaded cells. Cells were typed by multiple sequential primary immunocytochemistry at the end of the Ca2+ measurements. PACAP-27 increased [Ca2+]i by three different mechanisms, each one dominant in a given cell type. These involved Ca2+ entry or release from the stores and mediation through different second messenger pathways: (1) stimulation of Ca2+ entry mediated by cAMP was the main mechanism in somatotrophs; (2) Ca2+ release from the intracellular Ca2+ stores mediated by phospholipase C (PLC) was the dominant modality in gonadotrophs; (3) stimulation of Ca2+ entry not mediated by cAMP was the main mechanism in lactotrophs. A minor fraction of somatotrophs (11%) may also use mechanism 3. Corticotrophs and thyrotrophs exhibited weak responses to PACAP (<10% of the cells responded), which in all cases were mediated by mechanism 1. Mechanism 3 represents a novel effect of PACAP which cannot be explained by interaction with the conventional PACAP receptor families.
机译:我们比较了垂体腺苷酸环化酶激活多肽(PACAP-27)对原代培养的大鼠垂体前叶五种主要细胞类型的影响,方法是监测单装呋喃2的胞浆中Ca2 +浓度([Ca2 +] i)的变化。细胞。在Ca2 +测量结束时通过多次连续的一级免疫细胞化学对细胞进行分型。 PACAP-27通过三种不同的机制增加[Ca2 +] i,每种机制在给定的细胞类型中均占优势。这些涉及Ca 2+的进入或从储存中释放或通过不同的第二信使途径进行介导:(1)cAMP介导的Ca 2+进入的刺激是生长体的主要机制; (2)在促性腺激素中,磷脂酶C(PLC)介导的细胞内Ca2 +储存的Ca2 +释放是主要形式; (3)刺激不是由cAMP介导的Ca 2+进入是营养缺陷型的主要机制。极少数的植物营养体(11%)也可以使用机理3。皮质营养体和甲状腺营养体对PACAP的反应较弱(<10%的细胞响应),在所有情况下均由机理1介导。机理3代表了一种新的作用。无法通过与常规PACAP受体家族的相互作用来解释PACAP。

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