Department of Molecular Pharmacology, University of Groningen, Groningen, The Netherlands GRIAC Research Institute, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Department of Pulmonology, Leiden University Medical Center, Leiden, The Netherlands.
Thorax. 2015 Jul;70(7):668-76. doi: 10.1136/thoraxjnl-2014-205731. Epub 2015 May 20.
It has been shown that acetylcholine is both a neurotransmitter and acts as a local mediator, produced by airway cells including epithelial cells. In vivo studies have demonstrated an indirect role for acetylcholine in epithelial cell differentiation. Here, we aimed to investigate direct effects of endogenous non-neuronal acetylcholine on epithelial cell differentiation.
Human airway epithelial cells from healthy donors were cultured at an air-liquid interface (ALI). Cells were exposed to the muscarinic antagonist tiotropium (10 nM), interleukin (IL)-13 (1, 2 and 5 ng/mL), or a combination of IL-13 and tiotropium, during or after differentiation at the ALI.
Human airway epithelial cells expressed all components of the non-neuronal cholinergic system, suggesting acetylcholine production. Tiotropium had no effects on epithelial cell differentiation after air exposure. Differentiation into goblet cells was barely induced after air exposure. Therefore, IL-13 (1 ng/mL) was used to induce goblet cell metaplasia. IL-13 induced MUC5AC-positive cells (5-fold) and goblet cells (14-fold), as assessed by histochemistry, and MUC5AC gene expression (105-fold). These effects were partly prevented by tiotropium (47-92%). Goblet cell metaplasia was induced by IL-13 in a dose-dependent manner, which was inhibited by tiotropium. In addition, tiotropium reversed goblet cell metaplasia induced by 2 weeks of IL-13 exposure. IL-13 decreased forkhead box protein A2 (FoxA2) expression (1.6-fold) and increased FoxA3 (3.6-fold) and SAM-pointed domain-containing ETS transcription factor (SPDEF) (5.2-fold) expression. Tiotropium prevented the effects on FoxA2 and FoxA3, but not on SPDEF.
We demonstrate that tiotropium has no effects on epithelial cell differentiation after air exposure, but inhibits and reverses IL-13-induced goblet cell metaplasia, possibly via FoxA2 and FoxA3. This indicates that non-neuronal acetylcholine contributes to goblet cell differentiation by a direct effect on epithelial cells.
已经证明乙酰胆碱既是一种神经递质,也是一种局部介质,由包括上皮细胞在内的气道细胞产生。体内研究表明乙酰胆碱在上皮细胞分化中具有间接作用。在这里,我们旨在研究内源性非神经乙酰胆碱对上皮细胞分化的直接影响。
从健康供体的人呼吸道上皮细胞在气液界面(ALI)培养。细胞暴露于毒蕈碱拮抗剂噻托溴铵(10 nM)、白细胞介素(IL)-13(1、2 和 5 ng/mL)或 IL-13 和噻托溴铵的组合,在 ALI 分化期间或之后。
人呼吸道上皮细胞表达非神经胆碱能系统的所有成分,提示乙酰胆碱的产生。噻托溴铵在空气暴露后对上皮细胞分化没有影响。空气暴露后几乎没有诱导杯状细胞分化。因此,使用 IL-13(1 ng/mL)诱导杯状细胞化生。IL-13 诱导 MUC5AC 阳性细胞(5 倍)和杯状细胞(14 倍),通过组织化学评估,以及 MUC5AC 基因表达(105 倍)。这些作用部分被噻托溴铵(47-92%)预防。杯状细胞化生由 IL-13 呈剂量依赖性诱导,噻托溴铵抑制该作用。此外,噻托溴铵逆转了 2 周 IL-13 暴露诱导的杯状细胞化生。IL-13 降低叉头框蛋白 A2(FoxA2)表达(1.6 倍),增加 FoxA3(3.6 倍)和 SAM 点结构域包含 ETS 转录因子(SPDEF)(5.2 倍)表达。噻托溴铵预防了 FoxA2 和 FoxA3 的作用,但对 SPDEF 没有作用。
我们证明噻托溴铵在空气暴露后对上皮细胞分化没有影响,但抑制和逆转了 IL-13 诱导的杯状细胞化生,可能通过 FoxA2 和 FoxA3。这表明非神经乙酰胆碱通过对上皮细胞的直接作用促进杯状细胞分化。