河北医科大学学报

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凋亡细胞调控巨噬细胞表达IL-12家族细胞因子的水平

  

  1. 1.河北省承德市中心医院检验科,河北 承德 067000;2.河北医科大学基础医学院免疫学教研室,河北 石家庄 050017
  • 出版日期:2020-01-25 发布日期:2020-02-25
  • 作者简介:刘冰慧(1983-),女,蒙古族,河北承德人,河北省承德市中心医院主管检验师,医学硕士,从事临床检验学研究。
  • 基金资助:
    河北省医学科学研究重点课题(20160300)

Apoptotic cells regulate the level of IL-12 family in macrophages#br#

  1. 1.Department of Clinical Laboratory, Chengde Center Hospital, Hebei Province,Chengde
    067000, China; 2.Department of Immunology, the School of Basic Medicine Sciences,
    Hebei Medical University, Shijiazhuang 050017, China
  • Online:2020-01-25 Published:2020-02-25

摘要: [摘要]
目的  观察凋亡细胞对巨噬细胞中白细胞介素12 (interleukin-12,IL-12)家族细胞因子表达的影响。
方法  将小鼠巨噬细胞系RAW264.7(RAW 细胞)和小鼠腹腔巨噬细胞分别分为空白对照组、脂多糖(lipopolysaccharides,LPS)刺激组(LPS组)、凋亡细胞刺激组(apo组)、脂多糖+凋亡细胞刺激组(LPS+apo组),实时定量PCR检测各组细胞刺激前后mIL-12p35、mIL-12p40、mIL-23p19水平。采用酶联免疫吸附测定方法检测各组激活的RAW细胞培养液中IL-10、前列腺素E2(prostaglandin E2,PGE2)和转化生长因子β(transforming growth factor-β,TGF-β)的含量。
结果  RAW细胞和小鼠腹腔巨噬细胞LPS组IL-12p35、IL-12p40、IL-23p19 mRNA表达量高于空白对照组和apo组,LPS+apo组IL-12p35、IL-12p40、IL-23p19 mRNA表达量高于空白对照组和apo组,低于LPS组(P<0.05)。LPS组和LPS+apo组IL-10、PGE2、TGF-β浓度均高于对照组,LPS+apo组TGF-β浓度高于对照组和LPS组(P<0.05);LPS组和LPS+apo组IL-10、PGE2浓度差异无统计学意义(P>0.05)。
结论  凋亡细胞抑制活化巨噬细胞IL-12p35、IL-12p40、IL-23p19 mRNA的表达。凋亡细胞对IL-10和PGE2分泌无影响,但促进TGF-β的分泌。

关键词: 巨噬细胞, 凋亡细胞, 白细胞介素12

Abstract: [Abstract]Objective〖HTSS〗To investigate the effect of apoptotic cells on expression of interleukin-12(IL-12) family cytokines in macrophages.
Methods〖HTSS〗RAW264.7 (RAW cells) from the mouse macrophage cell lineage and mouse peritoneal macrophages were divided into 4 groups respectively: blank control group, lipopolysaccharide(LPS) stimulation group, apoptotic(apo) cell stimulation group, LPS+apo cell stimulation group, the levels of mIL-12p35, mIL-12p40 and mIL-23p19 in macrophage cell of each group before and after the stimulation were detected by real-time quantitative polymease chain reaction(PCR). The contents of IL-10, prostaglandin E2(PGE2) and transforming growth factor-β (TGF-β) in RAW cell supernatant were detected by enzyme linked immunosorbent assay(ELISA).
Results〖HTSS〗The mRNA expression level of IL-12p35, IL-12p40 and IL-23p19 in RAW cells or mouse peritoneal macrophages were higher in LPS group than in blank control group and apo group. The mRNA level of IL-12p35, IL-12p40 and IL-23p19 in the LPS+apo group were higher than those in the blank control group and in the apo group, and lower than those in the LPS group(P<0.05). The concentrations of IL-10, PGE2 and TGF-β in the LPS group or LPS+apo group were all higher than those in the control group, and  the concentrations of TGF-β in LPS+apo group were significantly higher than those in the LPS group(P<0.05), while the differences of IL-10 or PGE2 concentrations in the LPS group and LPS+apo group were not statistically significant(P>0.05).
Conclusion〖HTSS〗Apoptotic cells inhibit the expression of IL-12p35, IL-12p40 and IL-23p19 mRNA in activated macrophages. Apoptotic cells have no effect on the secretion of IL-10 and PGE2, but can promote the secretion of TGF-β in macrophages.

Key words: macrophages; apoptotic cell, interleukin-12