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血清素对培养的牛肺动脉平滑肌细胞生长的双重作用。

Dual effect of serotonin on growth of bovine pulmonary artery smooth muscle cells in culture.

作者信息

Lee S L, Wang W W, Moore B J, Fanburg B L

机构信息

Department of Medicine, New England Medical Center, Boston, Mass. 02111.

出版信息

Circ Res. 1991 May;68(5):1362-8. doi: 10.1161/01.res.68.5.1362.

Abstract

We have previously reported that serotonin (5-hydroxytryptamine [5HT]) alters cultured bovine pulmonary artery smooth muscle cell (SMC) configuration through two different regulatory mechanisms. We now report that 5HT also regulates SMC growth through these same two mechanisms--a stimulatory event initiated intracellularly and inhibition of growth resulting from a cell surface action. 5HT (1 microM) plus 0.1 mM iproniazid (a 5HT metabolic inhibitor) produced a severalfold stimulation of DNA synthesis (as measured by [3H]thymidine incorporation) of SMCs after a 17-24-hour incubation with only a slight elevation of cellular cAMP. This stimulatory effect responded synergistically with other growth factors including platelet-derived growth factor, fibroblast growth factor, and epidermal growth factor and was effectively reversed by 5HT uptake inhibition. It was not produced by 5-hydroxyindoleacetic acid, a metabolite of 5HT. In the presence of 1 microM 5HT plus 0.1 mM isobutylmethylxanthine (IBMX), cAMP was elevated eightfold, dendritic formation occurred, and [3H]thymidine labeling of SMCs was inhibited. Inhibition of labeling by [3H]thymidine was mimicked by other agents that elevated cellular cAMP (10 microM histamine, 1 microM isoproterenol plus 0.1 mM IBMX, and 10 microM forskolin) and by 1 mM dibutyryl cAMP. This inhibitory effect was not blocked by either inhibition of 5HT uptake or 5HT-receptor antagonists ketanserin (5HT2); methiothepin, spiperone, and mianserin (5HT1/5HT2); and 3-tropanyl-indole-3-carboxylate and 3-tropanyl-3,5-dichlorobenzoate (5HT3). However, similar to 5HT, the 5HT1A agonist, (+/-)-8-hydroxy-(+/-)-2-dipropylamino-8-hydroxy-1,2,3, 4-tetrahydronaphthalenehydrobromide, in association with IBMX, produced an elevation in cAMP and inhibition of labeling by [3H]thymidine. 5HT, in the presence of either iproniazid or IBMX, did not alter [Ca2+]i, indicating that [Ca2+]i was not a signal for either of these actions.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们之前曾报道,血清素(5-羟色胺[5HT])通过两种不同的调节机制改变培养的牛肺动脉平滑肌细胞(SMC)的形态。我们现在报道,5HT也通过这两种相同的机制调节SMC的生长——一种是细胞内启动的刺激事件,另一种是细胞表面作用导致的生长抑制。5HT(1微摩尔)加0.1毫摩尔异烟肼(一种5HT代谢抑制剂)在与细胞共孵育17 - 24小时后,对SMC的DNA合成(通过[3H]胸苷掺入法测定)产生了几倍的刺激,而细胞内cAMP仅略有升高。这种刺激作用与其他生长因子包括血小板衍生生长因子、成纤维细胞生长因子和表皮生长因子协同反应,并被5HT摄取抑制有效逆转。它不是由5HT的代谢产物5-羟吲哚乙酸产生的。在存在1微摩尔5HT加0.1毫摩尔异丁基甲基黄嘌呤(IBMX)的情况下,cAMP升高了八倍,出现了树突状形成,并且SMC的[3H]胸苷标记受到抑制。其他能升高细胞内cAMP的试剂(10微摩尔组胺、1微摩尔异丙肾上腺素加0.1毫摩尔IBMX以及10微摩尔福斯高林)和1毫摩尔二丁酰cAMP模拟了[3H]胸苷标记的抑制作用。这种抑制作用既不被5HT摄取抑制也不被5HT受体拮抗剂酮色林(5HT2)、甲硫哒嗪、螺哌隆和米安色林(5HT1/5HT2)以及3 - 托烷 - 吲哚 - 3 - 羧酸盐和3 - 托烷 - 3,5 - 二氯苯甲酸盐(5HT3)阻断。然而,与5HT类似,5HT1A激动剂(±)-8 - 羟基 - (±)-2 - 二丙基氨基 - 8 - 羟基 - 1,2,3,4 - 四氢萘氢溴酸盐与IBMX联合使用时,会使cAMP升高并抑制[3H]胸苷标记。在存在异烟肼或IBMX的情况下,5HT不会改变细胞内钙离子浓度([Ca2+]i),这表明[Ca2+]i不是这些作用的信号之一。(摘要截短于250字)

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