Department of Pharmacology, School of Medicine, Kyung Hee University, 26 Kyungheedae-ro, Dongdae-mun-gu, Seoul 02447, Korea.
Department of Medical Engineering, Graduate School, Kyung Hee University, 26 Kyungheedae-ro, Dongdae-mun-gu, Seoul 02447, Korea.
Toxins (Basel). 2021 Nov 1;13(11):773. doi: 10.3390/toxins13110773.
IL-13 induces mucus metaplasia, which causes airway obstruction in asthma. Bee venom (BV) and its components have shown anti-inflammatory effects in allergic diseases such as atopic dermatitis and asthma. In this study, we investigated the effect of BV on IL-13-induced mucus metaplasia through activation of the signal transducer and activator of transcription (STAT6), and regulation of SAM-pointed domain containing Ets-like factor (SPDEF) and forkhead box A2 (FOXA2) in the airway epithelia cell line A549. In A549 cells, BV (1.0 µg/mL) inhibited IL-13 (10 ng/mL)-induced AKT phosphorylation, increase in SPDEF protein expression, and decrease in FOXA2 protein expression-but not STAT6 phosphorylation. BV also prevented the IL-13-induced increase in mucin 5AC (MUC5AC) mRNA and protein expression. Moreover, we observed that inhibition of phosphoinositide 3 kinase (PI3K)/AKT using LY294002 (50 µM) could reverse the alterations in FOXA2 and MUC5AC expression -by IL-13 and BV. However, LY294002 did not affect IL-13- and BV-induced changes in SPDEF expression. These findings indicate that BV inhibits MUC5AC production through the regulation of SPDEF and FOXA2. The inhibition of MUC5AC production through FOXA2 is mediated via the suppression of PI3K/AKT activation by BV. BV may be helpful in the prevention of mucus metaplasia in asthma.
IL-13 诱导黏液化生,导致哮喘中的气道阻塞。蜂毒 (BV) 及其成分已显示出在特应性皮炎和哮喘等过敏性疾病中的抗炎作用。在这项研究中,我们通过激活信号转导和转录激活因子 (STAT6) 以及调节气道上皮细胞系 A549 中的含 SAM 点域的 Ets 样因子 (SPDEF) 和叉头框 A2 (FOXA2),研究了 BV 对 IL-13 诱导的黏液化生的影响。在 A549 细胞中,BV(1.0μg/mL)抑制了 IL-13(10ng/mL)诱导的 AKT 磷酸化、SPDEF 蛋白表达增加和 FOXA2 蛋白表达减少,但不抑制 STAT6 磷酸化。BV 还可防止 IL-13 诱导的粘蛋白 5AC(MUC5AC)mRNA 和蛋白表达增加。此外,我们观察到使用 LY294002(50μM)抑制磷酸肌醇 3 激酶 (PI3K)/AKT 可逆转 IL-13 和 BV 引起的 FOXA2 和 MUC5AC 表达的改变。然而,LY294002 不影响 IL-13 和 BV 诱导的 SPDEF 表达变化。这些发现表明,BV 通过调节 SPDEF 和 FOXA2 抑制 MUC5AC 的产生。BV 通过 FOXA2 抑制 MUC5AC 的产生是通过抑制 PI3K/AKT 激活来介导的。BV 可能有助于预防哮喘中的黏液化生。