Department of Respiratory Medicine, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
J Allergy Clin Immunol. 2011 Sep;128(3):626-34.e1-5. doi: 10.1016/j.jaci.2011.04.032. Epub 2011 Jul 18.
Cold air stimulus is a major environmental factor that exacerbates chronic inflammatory airway diseases, such as chronic obstructive pulmonary disease (COPD) and asthma. At the molecular level, cold is detected by transient receptor potential melastatin 8 (TRPM8). To date, TRPM8 expression has not been characterized in the airway epithelium of patients with COPD. The role of TRPM8 channels in a series of airway responses induced by cold stimuli and the molecular and biochemical pathways of TRPM8 in regulating cold-induced responses are largely unknown.
We sought to explore the role of TRPM8 in cold air-provoked mucus hypersecretion and the potential signaling pathway involved in this process.
The expression of TRPM8 in the bronchial epithelium was examined by means of immunohistochemistry, RT-PCR, and Western blotting. TRPM8 receptor function and hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) were characterized by means of Ca(2+) imaging and spatiotemporal dynamics of phospholipase C (PLC) δ1-pleckstrin homology-green fluorescent protein, respectively. The expression of MUC5AC mRNA and MUC5AC mucin protein was measured by using real-time PCR and ELISA, respectively. Four serine residues in the myristoylated alanine-rich C kinase substrate (MARCKS)-phosphorylation site domain were mutated to identify the function of MARCKS in TRPM8-mediated airway mucus hypersecretion.
TRPM8 protein and mRNA expression were significantly increased in patients with COPD compared with expression seen in healthy subjects. Cold produced robust increases in intracellular Ca(2+) levels and promoted translocation of PLCδ1-pleckstrin homology-green fluorescent protein. Cold increased expression of MUC5AC mRNA and intracellular and secreted MUC5AC protein in a nonsustained way. Phosphorylation site domain-mutant MARCKS cDNA hindered MUC5AC secretion induced by cold.
These results indicate that the TRPM8 receptor is involved in cold-induced mucus hypersecretion through the Ca(2+)-PLC-PIP2-MARCKS signaling pathway.
冷空气刺激是加重慢性炎症性气道疾病(如慢性阻塞性肺疾病[COPD]和哮喘)的主要环境因素。在分子水平上,冷由瞬时受体电位 melastatin 8(TRPM8)检测。迄今为止,尚未对 COPD 患者的气道上皮中的 TRPM8 表达进行表征。TRPM8 通道在冷刺激诱导的一系列气道反应中的作用以及调节冷诱导反应的 TRPM8 的分子和生化途径在很大程度上是未知的。
我们旨在探讨 TRPM8 在冷空气诱发的黏液过度分泌中的作用以及该过程中涉及的潜在信号通路。
通过免疫组织化学、RT-PCR 和 Western blot 检查支气管上皮中的 TRPM8 表达。通过 Ca(2+)成像和磷脂酶 C(PLC)δ1-pleckstrin 同源性-绿色荧光蛋白的时空动力学分别表征 TRPM8 受体功能和磷脂酰肌醇 4,5-二磷酸(PIP2)的水解。通过实时 PCR 和 ELISA 分别测量 MUC5AC mRNA 和 MUC5AC 粘蛋白蛋白的表达。将豆蔻酰化丙氨酸丰富的 C 激酶底物(MARCKS)-磷酸化位点结构域中的四个丝氨酸残基突变为鉴定 MARCKS 在 TRPM8 介导的气道黏液过度分泌中的功能。
与健康受试者相比,COPD 患者的 TRPM8 蛋白和 mRNA 表达显著增加。冷刺激可引起细胞内 Ca(2+)水平的剧烈增加,并促进 PLCδ1-pleckstrin 同源性-绿色荧光蛋白的易位。冷刺激可引起 MUC5AC mRNA 以及细胞内和分泌的 MUC5AC 蛋白的非持续增加。冷刺激诱导的 MARCKS 磷酸化位点结构域突变 cDNA 阻碍 MUC5AC 分泌。
这些结果表明,TRPM8 受体通过 Ca(2+)-PLC-PIP2-MARCKS 信号通路参与冷诱导的黏液过度分泌。