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神经肽YY1受体通过磷脂酶C依赖性途径介导猪主动脉平滑肌细胞内钙离子浓度升高。

Neuropeptide YY1 receptors-mediated increase in intracellular Ca2+ concentration via phospholipase C-dependent pathway in porcine aortic smooth muscle cells.

作者信息

Shigeri Y, Nakajima S, Fujimoto M

机构信息

Shionogi Research Laboratories, Shionogi and Co., Ltd., Osaka.

出版信息

J Biochem. 1995 Sep;118(3):515-20. doi: 10.1093/oxfordjournals.jbchem.a124938.

Abstract

In porcine aortic smooth muscle cells, neuropeptide Y (NPY) stimulates mobilization of CA(2+) from intracellular store sites via Y1 receptors. However, it has been debated whether or not Ca(2+) mobilization by Y1 receptors depends on the generation of inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] following activation of phospholipase C. To examine this question, we studied the effect of U73122, an inhibitor of phospholipase C-mediated inositol phosphate accumulation on the NPY-induced rise in cytosolic free Ca(2+) concentration ([Ca(2+)]i) in comparison with that on angiotensin II (AII)-induced [Ca(2+)]i increase, which is dependent on Ins(1,4,5)P3 generation. Digital-imaging microscopy study using the Ca(2+)-sensitive dye fura-2 revealed that application of AII induced a rapid but transient [Ca(2+)]i increase in a single cell, arising from intracellular calcium stores. Application of NPY to the same cell induced a [Ca(2+)]i rise with a pattern similar to that induced by AII. AII increased the formation of Ins(1,4,5)P3 by about 3.0 fold, while the NPY-induced [Ca(2+) formation was very small. U73122 completely inhibited not only Ins(1,4,5)P3 synthesis, but also Ca(2+) mobilization induced by either agonist. The effect of U73122 on the NPY-induced Ca(2+)i increase was about 10-fold more potent that on the AII-induced one. U73343, an inactive analog of U733343, had no influence on any of the AII- and NPY-mediated effects. Herbimycin A completely inhibited the platelet-derived growth factor-induced [Ca(2+]i increase but had no effect on the NPY-induced [Ca(2+)]i increase, indicating that phospholipase C-gamma is not involved in the NPY effect. These results suggest that NPY-induced Ca2+ mobilization from intracellular stores in porcine smooth muscle cells is secondary to the very small generation of Ins(1,4,5)P3 following stimulation of phospholipase C-beta, which may account for the hypersensitivity of the NPY effect to U73122.

摘要

在猪主动脉平滑肌细胞中,神经肽Y(NPY)通过Y1受体刺激细胞内储存部位的Ca(2+)释放。然而,Y1受体介导的Ca(2+)释放是否依赖于磷脂酶C激活后肌醇1,4,5-三磷酸[Ins(1,4,5)P3]的生成一直存在争议。为了研究这个问题,我们研究了磷脂酶C介导的肌醇磷酸积累抑制剂U73122对NPY诱导的胞质游离Ca(2+)浓度([Ca(2+)]i)升高的影响,并与血管紧张素II(AII)诱导的[Ca(2+)]i升高进行比较,后者依赖于Ins(1,4,5)P3的生成。使用Ca(2+)敏感染料fura-2进行的数字成像显微镜研究表明,应用AII可诱导单个细胞内Ca(2+)迅速但短暂升高,这源于细胞内钙储存。对同一细胞应用NPY可诱导[Ca(2+)]i升高,其模式与AII诱导的相似。AII使Ins(1,4,5)P3的形成增加约3.0倍,而NPY诱导的[Ca(2+)]形成非常小。U73122不仅完全抑制了Ins(1,4,5)P3的合成,还抑制了两种激动剂诱导的Ca(2+)释放。U73122对NPY诱导的Ca(2+)i升高的作用比对AII诱导的作用强约10倍。U73343是U73122的无活性类似物,对AII和NPY介导的任何效应均无影响。赫伯霉素A完全抑制血小板衍生生长因子诱导的[Ca(2+)]i升高,但对NPY诱导的[Ca(2+)]i升高无影响,表明磷脂酶C-γ不参与NPY的作用。这些结果表明,NPY诱导的猪平滑肌细胞内钙储存释放Ca2+是磷脂酶C-β刺激后Ins(1,4,5)P3生成极少的继发结果,这可能解释了NPY效应对U73122的超敏感性。

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