| 注册
首页|期刊导航|中国医科大学学报|利拉鲁肽对高糖诱导的炎症单核细胞亚群分化的影响

利拉鲁肽对高糖诱导的炎症单核细胞亚群分化的影响

申亚丽 蒋昆 张敏丽 苏艳红 张大庆

中国医科大学学报2017,Vol.46Issue(9):773-778,6.
中国医科大学学报2017,Vol.46Issue(9):773-778,6.DOI:10.12007/j.issn.0258-4646.2017.09.002

利拉鲁肽对高糖诱导的炎症单核细胞亚群分化的影响

Liraglutide Inhibits Inflammatory Monocyte Differentiation Induced by High Glucose

申亚丽 1蒋昆 1张敏丽 1苏艳红 1张大庆1

作者信息

  • 1. 中国医科大学附属盛京医院心内科,沈阳110004
  • 折叠

摘要

Abstract

Objective To explore the mechanism by which liraglutide modulated the differentiation of monocyte subsets in high glucose (HG) conditions.Methods Primary mouse splenocyte suspensions were cultured in HG conditions induced by IFN-γ in the presence or absence of liraglutide.The cells were harvested,co-incubated with antibodies,and analyzed on a BD FACS Calibur.Mononuclear cells (MNCs) were gated according to lower granularity and larger size by SSC and FSC.Monocytes (MCs) were defined as CD11b+MNC and divided into three subsets based on Ly6C expression:Ly6Clow,Ly6Cmid,and Ly6Chi.ROS production in Ly6C+ and Ly6C-MCs was detected by 2',7'-dichlorofluorescein-diacetate (DCFH-DA) staining and ROS-containing MCs were identified as DCF+ cells in both Ly6C+ and Ly6C-MCs.Results HG (15 mmol/L,25 mmol/L,35 mmol/L) dose-dependently increased Ly6Chi and Ly6Cmid MC differentiation and also enhanced the production of ROS in Ly6C+MCs.Liraglutide (100 U,200 U) dose-dependently inhibited HG-induced Ly6Chi and Ly6Cmid MC differentiation and also promoted the differentiation of Ly6Clow MCs.Moreover,liraglutide significantly inhibited HG-induced ROS production in Ly6C+ MCs.Conclusion Liraglutide treatment significantly inhibited inflammatory MC diferentiation induced by HG and also reduced ROS production in inflammatory MCs.

关键词

利拉鲁肽/糖尿病/氧化应激/炎症单核细胞

Key words

liraglutide/diabetes mellitus/oxidative stress/inflammatory monocyte

分类

医药卫生

引用本文复制引用

申亚丽,蒋昆,张敏丽,苏艳红,张大庆..利拉鲁肽对高糖诱导的炎症单核细胞亚群分化的影响[J].中国医科大学学报,2017,46(9):773-778,6.

基金项目

国家自然科学基金(81200199) (81200199)

辽宁省高等学校杰出青年学者成长计划(LJQ2015117) (LJQ2015117)

中国医科大学学报

OA北大核心CSCDCSTPCD

0258-4646

访问量0
|
下载量0
段落导航相关论文