Department of Medical Science, College of Medicine, Graduate School of Yeungnam University, Daegu, Republic of Korea.
Department of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, Yeungnam University, Daegu, Republic of Korea; Regional Center for Respiratory Diseases, Yeungnam University Medical Center, Daegu, Republic of Korea.
Biochem Biophys Res Commun. 2018 May 15;499(3):655-661. doi: 10.1016/j.bbrc.2018.03.206. Epub 2018 Mar 31.
Adipokines, a group of proteins including leptin, visfatin, resistin, and adiponectin, are produced by adipocytes. Among adipokines, resistin is implicated in insulin resistance and inflammatory response modulation. Mucus hypersecretion has been greatly linked to airway diseases, such as asthma, chronic obstructive pulmonary disease, and rhinosinusitis. Increasing evidence has indicated that adipokines, such as leptin and visfatin, play important regulatory roles in various biological processes involved in mucus secretion. However, the effects of resistin on mucin expression in human airway epithelial cells, as well as the underlying mechanisms, have not been investigated yet. We showed that resistin affected mucin expression in human airway epithelial cells via the mitogen-activated protein kinase/nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathway. Resistin increased MUC5AC and MUC5B expression in NCI-H292 and primary human nasal epithelial cells. Additionally, it significantly increased the phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2), p38, and NF-κB. ERK1/2 and p38 specific inhibitors significantly attenuated resistin-induced MUC5AC/5B expression; however, NF-κB inhibitor reduced resistin-induced MUC5AC, but not MUC5B, expression. Knockdown of ERK1, ERK2, and p38 by ERK1, ERK2, and p38 small interfering RNA (siRNA), respectively, significantly blocked resistin-induced MUC5AC and MUC5B mRNA expression. In addition, NF-κB siRNA attenuated resistin-induced MUC5AC, but not MUC5B, expression. These results suggested that resistin induced MUC5AC and MUC5B expression via activation of different signaling pathways in human airway epithelial cells.
脂肪因子是一组由脂肪细胞产生的蛋白质,包括瘦素、内脂素、抵抗素和脂联素。在脂肪因子中,抵抗素与胰岛素抵抗和炎症反应调节有关。黏液过度分泌与气道疾病密切相关,如哮喘、慢性阻塞性肺疾病和鼻鼻窦炎。越来越多的证据表明,脂肪因子(如瘦素和内脂素)在涉及黏液分泌的各种生物过程中发挥重要的调节作用。然而,抵抗素对人呼吸道上皮细胞黏蛋白表达的影响及其潜在机制尚未得到研究。我们发现抵抗素通过丝裂原活化蛋白激酶/核因子 kappa-轻链增强子的激活 B 细胞(NF-κB)途径影响人呼吸道上皮细胞的黏蛋白表达。抵抗素增加了 NCI-H292 和原代人鼻上皮细胞中 MUC5AC 和 MUC5B 的表达。此外,它还显著增加了细胞外信号调节激酶 1/2(ERK1/2)、p38 和 NF-κB 的磷酸化。ERK1/2 和 p38 的特异性抑制剂显著减弱了抵抗素诱导的 MUC5AC/5B 表达;然而,NF-κB 抑制剂减少了抵抗素诱导的 MUC5AC,但不减少 MUC5B 的表达。ERK1、ERK2 和 p38 的小干扰 RNA(siRNA)分别敲低 ERK1、ERK2 和 p38,显著阻断了抵抗素诱导的 MUC5AC 和 MUC5B mRNA 表达。此外,NF-κB siRNA 减弱了抵抗素诱导的 MUC5AC,但不减少 MUC5B 的表达。这些结果表明,抵抗素通过激活人呼吸道上皮细胞中的不同信号通路诱导 MUC5AC 和 MUC5B 的表达。