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全反式维甲酸对单核细胞中Th1和Th2相关趋化因子产生的影响。

Effects of all-trans retinoic acid on Th1- and Th2-related chemokines production in monocytes.

作者信息

Tsai Yu-Chien, Chang Hui-Wen, Chang Tai-Tsung, Lee Min-Sheng, Chu Yu-Te, Hung Chih-Hsing

机构信息

Department of Pediatrics, Chi-Mei Medical Center, Tainan, Taiwan, Republic of China.

出版信息

Inflammation. 2008 Dec;31(6):428-33. doi: 10.1007/s10753-008-9095-x.

Abstract

Low vitamin C and reduced alpha-carotene intake are associated with increased asthma risk in children. In addition, mean serum vitamin A concentrations are significantly lower in asthmatic children than in controls. All-trans retinoic acid (ATRA) is a derivative of vitamin A. Macrophage-derived chemokine (MDC) is a T helper cell-type 2 (Th2)-related chemokine involved in the recruitment of Th2 cells toward inflammatory sites. On the other hand, Th1-related chemokine, interferon-inducible protein 10 (IP-10)/CXCL10 is also important in allergic inflammation. Both Th1- and Th2-related chemokines play an important role in allergic asthma. To survey whether ATRA and ascorbic acid effect Th1- and Th2-related chemokine expression in monocytes. To test this, THP-1 cells were pre-treated with ATRA or ascorbic acid and stimulated by lipopolysaccharide (LPS) or poly I:C. Supernatants were measured for Th2-related (MDC) and Th1-related (IP-10) chemokine concentrations by ELISA. The effects of ATRA on mitogen-activated protein kinase (MAPK) and NFkb were evaluated with Western blotting. After stimulation, ATRA significantly down-regulated MDC and IP-10 in a dose-dependent manner. Similarly, ascorbic acid reduced the LPS-induced changes in MDC but only with a high dose. However, asorbic acid had no effect on IP-10 changes either induced by LPS or poly I:C. RT-PCR showed ATRA inhibited IP-10 expression through decreasing the level of transcription. Furthermore, ATRA suppressed the expression of LPS-stimulated c-Raf, MKK1/2 and ERK expression of THP-1 cells. In conclusion, ATRA suppressed Th2- and Th1-related chemokines expression in THP-1 cells, at least in part via the c-Raf-MKK1/2-ERK/MAPK pathway.

摘要

维生素C水平低和α-胡萝卜素摄入量减少与儿童哮喘风险增加有关。此外,哮喘儿童的血清维生素A平均浓度显著低于对照组。全反式维甲酸(ATRA)是维生素A的衍生物。巨噬细胞衍生趋化因子(MDC)是一种与2型辅助性T细胞(Th2)相关的趋化因子,参与Th2细胞向炎症部位的募集。另一方面,与Th1相关的趋化因子,即干扰素诱导蛋白10(IP-10)/CXCL10在过敏性炎症中也很重要。Th1和Th2相关趋化因子在过敏性哮喘中均起重要作用。旨在研究ATRA和抗坏血酸是否影响单核细胞中Th1和Th2相关趋化因子的表达。为验证此点,THP-1细胞先用ATRA或抗坏血酸预处理,然后用脂多糖(LPS)或聚肌胞苷酸(poly I:C)刺激。通过酶联免疫吸附测定(ELISA)测量上清液中Th2相关(MDC)和Th1相关(IP-10)趋化因子的浓度。用蛋白质免疫印迹法评估ATRA对丝裂原活化蛋白激酶(MAPK)和核因子κB(NFkb)的影响。刺激后,ATRA以剂量依赖性方式显著下调MDC和IP-10。同样,抗坏血酸可降低LPS诱导的MDC变化,但仅在高剂量时有效。然而,抗坏血酸对LPS或poly I:C诱导的IP-10变化均无影响。逆转录聚合酶链反应(RT-PCR)显示ATRA通过降低转录水平抑制IP-10表达。此外,ATRA抑制THP-1细胞中LPS刺激的c-Raf、MKK1/2和ERK的表达。总之,ATRA至少部分通过c-Raf-MKK1/2-ERK/MAPK途径抑制THP-1细胞中Th2和Th1相关趋化因子的表达。

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