{"title":"尼古丁通过HMGB1/RAGE诱导人气道上皮细胞分泌TGF-β1和FGF-2","authors":"W. Zou, Xiaoqian Wang, Qing Sheng, Xiaoting Zhou","doi":"10.3760/CMA.J.ISSN.1673-436X.2020.05.008","DOIUrl":null,"url":null,"abstract":"Objective \nTo test whether nicotine induces the secretion of transforming growth factor-β1 (TGF-β1)and fibroblast growth factor 2 (FGF-2) in HBECs in vitro via the high mobility group protein B1 (HMGB1)/receptor for advanced glycation end products (RAGE) signaling pathway. \n \n \nMethods \nCultured HBECs were exposed to nicotine (6×10-6 mol/L) for 24 h. The secretion of HMGB1, TGF-β1 and FGF-2 was assessed by ELISA, the expression of RAGE was assessed by Western blotting.HBECs were either transfected with a small interfering RNA (siRNA) targeting HMGB1 for 48 h or incubated with anti-RAGE antibodies for 1 h and subsequently stimulated with nicotine for 24 h, then the secretion of HMGB1, TGF-β1 and FGF-2 was assessed by ELISA, the expression of RAGE was assessed by Western blotting. \n \n \nResults \nWe showed that cells exposed to nicotine for 24 h exhibited significantly increased HMGB1, TGF-β1 and FGF-2 secretion and RAGE expression.The HMGB1 siRNA prevented these effects.Furthermore, anti-RAGE antibodies significantly decreased the secretion of TGF-β1 and FGF-2 from HBECs. \n \n \nConclusions \nThese results suggest that nicotine induces the secretion of TGF-β1 and FGF-2 in HBECs via the HMGB1/RAGE signaling pathway. \n \n \nKey words: \nNicotine; Transforming growth factor beta1; Fibroblast growth factor 2; Human bronchial epithelial cells; High mobility group protein B1/Receptor for advanced glycation end products","PeriodicalId":10004,"journal":{"name":"Chinese Journal of Asthma","volume":"46 1","pages":"368-372"},"PeriodicalIF":0.0000,"publicationDate":"2020-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nicotine induces the secretion of TGF-β1 and FGF-2 via HMGB1/RAGE in human airway epithelial cells\",\"authors\":\"W. Zou, Xiaoqian Wang, Qing Sheng, Xiaoting Zhou\",\"doi\":\"10.3760/CMA.J.ISSN.1673-436X.2020.05.008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective \\nTo test whether nicotine induces the secretion of transforming growth factor-β1 (TGF-β1)and fibroblast growth factor 2 (FGF-2) in HBECs in vitro via the high mobility group protein B1 (HMGB1)/receptor for advanced glycation end products (RAGE) signaling pathway. \\n \\n \\nMethods \\nCultured HBECs were exposed to nicotine (6×10-6 mol/L) for 24 h. The secretion of HMGB1, TGF-β1 and FGF-2 was assessed by ELISA, the expression of RAGE was assessed by Western blotting.HBECs were either transfected with a small interfering RNA (siRNA) targeting HMGB1 for 48 h or incubated with anti-RAGE antibodies for 1 h and subsequently stimulated with nicotine for 24 h, then the secretion of HMGB1, TGF-β1 and FGF-2 was assessed by ELISA, the expression of RAGE was assessed by Western blotting. \\n \\n \\nResults \\nWe showed that cells exposed to nicotine for 24 h exhibited significantly increased HMGB1, TGF-β1 and FGF-2 secretion and RAGE expression.The HMGB1 siRNA prevented these effects.Furthermore, anti-RAGE antibodies significantly decreased the secretion of TGF-β1 and FGF-2 from HBECs. \\n \\n \\nConclusions \\nThese results suggest that nicotine induces the secretion of TGF-β1 and FGF-2 in HBECs via the HMGB1/RAGE signaling pathway. \\n \\n \\nKey words: \\nNicotine; Transforming growth factor beta1; Fibroblast growth factor 2; Human bronchial epithelial cells; High mobility group protein B1/Receptor for advanced glycation end products\",\"PeriodicalId\":10004,\"journal\":{\"name\":\"Chinese Journal of Asthma\",\"volume\":\"46 1\",\"pages\":\"368-372\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-03-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Asthma\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3760/CMA.J.ISSN.1673-436X.2020.05.008\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Asthma","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.1673-436X.2020.05.008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Nicotine induces the secretion of TGF-β1 and FGF-2 via HMGB1/RAGE in human airway epithelial cells
Objective
To test whether nicotine induces the secretion of transforming growth factor-β1 (TGF-β1)and fibroblast growth factor 2 (FGF-2) in HBECs in vitro via the high mobility group protein B1 (HMGB1)/receptor for advanced glycation end products (RAGE) signaling pathway.
Methods
Cultured HBECs were exposed to nicotine (6×10-6 mol/L) for 24 h. The secretion of HMGB1, TGF-β1 and FGF-2 was assessed by ELISA, the expression of RAGE was assessed by Western blotting.HBECs were either transfected with a small interfering RNA (siRNA) targeting HMGB1 for 48 h or incubated with anti-RAGE antibodies for 1 h and subsequently stimulated with nicotine for 24 h, then the secretion of HMGB1, TGF-β1 and FGF-2 was assessed by ELISA, the expression of RAGE was assessed by Western blotting.
Results
We showed that cells exposed to nicotine for 24 h exhibited significantly increased HMGB1, TGF-β1 and FGF-2 secretion and RAGE expression.The HMGB1 siRNA prevented these effects.Furthermore, anti-RAGE antibodies significantly decreased the secretion of TGF-β1 and FGF-2 from HBECs.
Conclusions
These results suggest that nicotine induces the secretion of TGF-β1 and FGF-2 in HBECs via the HMGB1/RAGE signaling pathway.
Key words:
Nicotine; Transforming growth factor beta1; Fibroblast growth factor 2; Human bronchial epithelial cells; High mobility group protein B1/Receptor for advanced glycation end products