首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Effect of CSE on M1/M2 polarization in alveolar and peritoneal macrophages at different concentrations and exposure in vitro
【24h】

Effect of CSE on M1/M2 polarization in alveolar and peritoneal macrophages at different concentrations and exposure in vitro

机译:CSE对不同浓度和暴露的肺泡和腹膜巨噬细胞M1 / M2偏振中的影响

获取原文
获取原文并翻译 | 示例
           

摘要

Cigarette smoke exposure is one of the main etiologies for chronic obstructive pulmonary disease. Moreover, cigarette smoke participates in disease progression by inducing abnormal macrophage polarization; however, the effects of cigarette smoke on M1/M2 macrophage polarization have not been established. The aim of the current study was to determine the effects of cigarette smoke extract (CSE) on M1/M2 macrophage polarization in alveolar and peritoneal macrophages (AM and PM, respectively) at different concentrations and exposure times. Rat AM and PM were cultured with CSE at different concentrations. CCK-8 was used as an indicator of cell viability, and mRNA expression of M1 (iNOS, TNF-alpha, and IL-1 beta) and M2 markers (arg-1, CD206, and TGF-beta 1) were measured at 3, 6, 9, 12, and 24 h using qPCR. Expressions of CD86 and CD206 proteins at 12 h were determined using flow cytometry, and the iNOS/arg-1 ratio was used to determine the polarization dominance of M1 and M2. M2 subtypes were detected at 12 h using qPCR and flow cytometry. CSE increased the expression of iNOS, TNF-alpha, and IL-1 beta mRNA, and the proportion of CD86-positive cells in AM and PM promoted M1 polarization, and M1 polarization was continuously enhanced as exposure time and concentration increased. CSE reduced the expression of arg-1, CD206, and TGF-beta 1 mRNA and the proportion of CD206-positive cells in AM and PM and inhibited M2 polarization. At 9-24 h of CSE exposure, the expression of arg-1 in AM and PM gradually increased, showing tendency towards activation of M2 polarization. Besides, CSE might induce M2b and M2d polarization at 12 h. After 12 h of CSE exposure, transformation from M1 to M2 polarization dominance was shown in AM; however, M1 polarization was continuously enhanced in PM within 24 h of CSE exposure. CSE promoted M1 polarization in macrophages, exhibiting dynamic regulatory effects on M2 polarization, first as a suppressor and then as a promoter. The polarization change induced by CSE on AM was more sensitive than PM.
机译:香烟烟雾暴露是慢性阻塞性肺病的主要病因之一。此外,卷烟烟雾通过诱导异常巨噬细胞极化参与疾病进展;然而,尚未建立卷烟烟雾对M1 / M2巨噬细胞极化的影响。目前研究的目的是在不同浓度和暴露时间确定卷烟烟雾提取物(CSE)对肺泡和腹膜巨噬细胞(AM和PM)的影响。大鼠AM和PM以不同浓度的CSE培养。 CCK-8用作细胞活力的指标,并在3点测量M1(InOS,TNF-α和IL-1β)和M2标记物(Arg-1,CD206和TGF-Beta 1)的mRNA表达,6,9,12和24小时使用QPCR。使用流式细胞术测定CD86和CD206蛋白的表达,使用流式细胞术测定,使用INOS / ARG-1比率来确定M1和M2的偏振优势。使用QPCR和流式细胞术在12小时内检测M2亚型。 CSE增加了InOS,TNF-α和IL-1βmRNA的表达,以及AM和PM促进的M1偏振中的CD86阳性细胞的比例,并且在暴露时间和浓度增加时连续增强M1偏振。 CSE降低了ARG-1,CD206和TGF-β1mRNA的表达和AM和PM中CD206阳性细胞的比例并抑制M2偏振。在CSE暴露的9-24小时,ARG-1在AM和PM的表达逐渐增加,逐渐增加,显示出M2极化激活的趋势。此外,CSE可能会在12小时内诱导M2B和M2D偏振。在CSE暴露12小时后,AM显示来自M1至M2偏振偏振的转化;然而,在CSE暴露的24小时内在PM内连续增强M1极化。 CSE在巨噬细胞中促进M1偏振,表现出对M2偏振的动态调节作用,首先作为抑制剂,然后作为启动子。 CSE诱导的偏振变化比PM更敏感。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号