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血清素通过一条不依赖乙酰胆碱的途径增加小鼠气管中纤毛驱动的颗粒运输。

Serotonin increases cilia-driven particle transport via an acetylcholine-independent pathway in the mouse trachea.

作者信息

König Peter, Krain Benjamin, Krasteva Gabriela, Kummer Wolfgang

机构信息

Institut für Anatomie, Zentrum für medizinische Struktur- und Zellbiologie, Universität zu Lübeck, Lübeck, Germany.

出版信息

PLoS One. 2009;4(3):e4938. doi: 10.1371/journal.pone.0004938. Epub 2009 Mar 17.

Abstract

BACKGROUND

Mucociliary clearance in the airways is driven by the coordinated beating of ciliated cells. Classical neuromediators such as noradrenalin and acetylcholine increase ciliary beat frequency and thus cilia-driven transport. Despite the fact that the neuromediator serotonin is ciliostimulatory in invertebrates and has been implied in releasing acetylcholine from the airway epithelium, its role in regulating cilia function in vertebrate airways is not established.

METHODOLOGY/PRINCIPAL FINDINGS: We examined the effects of serotonin on ciliary beat frequency and cilia-driven particle transport in the acutely excised submerged mouse trachea and determined the sources of serotonin in this tissue by immunohistochemistry. Serotonin (100 microM) increased cilary beat frequency (8.9+/-1.2 Hz to 17.0+/-2.7 Hz) and particle transport speed (38.9+/-4.6 microm/s to 83.4+/-8.3 microm/s) to an extent that was comparable to a supramaximal dose of ATP. The increase in particle transport speed was totally prevented by methysergide (100 microM). Blockade of muscarinic receptors by atropine (1 microM) did not reduce the effect of serotonin, although it was effective in preventing the increase in particle transport speed mediated by muscarine (100 microM). Immunohistochemistry demonstrated serotonin in mast cells pointing towards mast cells and platelets as possible endogenous sources of serotonin.

CONCLUSIONS/SIGNIFICANCE: These results indicate that serotonin is a likely endogenous mediator that can increase cilia-driven transport independent from acetylcholine during activation of mast cells and platelets.

摘要

背景

气道中的黏液纤毛清除是由纤毛细胞的协同摆动驱动的。经典神经介质如去甲肾上腺素和乙酰胆碱可增加纤毛摆动频率,从而促进纤毛驱动的转运。尽管神经介质5-羟色胺在无脊椎动物中具有纤毛刺激作用,并被认为可从气道上皮释放乙酰胆碱,但其在调节脊椎动物气道纤毛功能中的作用尚未明确。

方法/主要发现:我们研究了5-羟色胺对急性切除并浸没的小鼠气管中纤毛摆动频率和纤毛驱动的颗粒转运的影响,并通过免疫组织化学确定了该组织中5-羟色胺的来源。5-羟色胺(100微摩尔)可增加纤毛摆动频率(从8.9±1.2赫兹增加到17.0±2.7赫兹)和颗粒转运速度(从38.9±4.6微米/秒增加到83.4±8.3微米/秒),其程度与超最大剂量的ATP相当。甲基麦角新碱(100微摩尔)可完全阻止颗粒转运速度的增加。阿托品(1微摩尔)阻断毒蕈碱受体并不能降低5-羟色胺的作用,尽管它能有效阻止毒蕈碱(100微摩尔)介导的颗粒转运速度增加。免疫组织化学显示肥大细胞中有5-羟色胺,表明肥大细胞和血小板可能是5-羟色胺的内源性来源。

结论/意义:这些结果表明,5-羟色胺可能是一种内源性介质,在肥大细胞和血小板激活过程中,可独立于乙酰胆碱增加纤毛驱动的转运。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c53/2654158/2ab302354baa/pone.0004938.g001.jpg

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